Dietary Polyphenols and Their Effects on Cell Biochemistry and Pathophysiology 2014View this Special Issue
Review Article | Open Access
Swapna Upadhyay, Madhulika Dixit, "Role of Polyphenols and Other Phytochemicals on Molecular Signaling", Oxidative Medicine and Cellular Longevity, vol. 2015, Article ID 504253, 15 pages, 2015. https://doi.org/10.1155/2015/504253
Role of Polyphenols and Other Phytochemicals on Molecular Signaling
Optimized nutrition through supplementation of diet with plant derived phytochemicals has attracted significant attention to prevent the onset of many chronic diseases including cardiovascular impairments, cancer, and metabolic disorder. These phytonutrients alone or in combination with others are believed to impart beneficial effects and play pivotal role in metabolic abnormalities such as dyslipidemia, insulin resistance, hypertension, glucose intolerance, systemic inflammation, and oxidative stress. Epidemiological and preclinical studies demonstrated that fruits, vegetables, and beverages rich in carotenoids, isoflavones, phytoestrogens, and phytosterols delay the onset of atherosclerosis or act as a chemoprotective agent by interacting with the underlying pathomechanisms. Phytochemicals exert their beneficial effects either by reducing the circulating levels of cholesterol or by inhibiting lipid oxidation, while others exhibit anti-inflammatory and antiplatelet activities. Additionally, they reduce neointimal thickening by inhibiting proliferation of smooth muscle cells and also improve endothelium dependent vasorelaxation by modulating bioavailability of nitric-oxide and voltage-gated ion channels. However, detailed and profound knowledge on specific molecular targets of each phytochemical is very important to ensure safe use of these active compounds as a therapeutic agent. Thus, this paper reviews the active antioxidative, antiproliferative, anti-inflammatory, or antiangiogenesis role of various phytochemicals for prevention of chronic diseases.
Overwhelming evidence from epidemiological, in vivo, in vitro, and clinical trial data indicates that the plant-based diet can reduce the risk of chronic diseases (e.g., cardiovascular disease, hypertension, diabetes, and cancer) due to presence of biologically active plant compounds or phytochemicals. Steinmetz and Potter identified more than a dozen classes of phytochemicals from plant based diets (fruits, vegetable, nuts, etc.), such as carotenoids, phenolic compounds (flavonoids, isoflavonoids, and lignin), phenolic acid, phytosterols and phytostanols, tocotrienols, organosulfur compounds, and nondigestible carbohydrates (dietary fiber, Table 1) . According to many researchers regular consumption of diet rich in vegetables, fruits, whole grains, herbs, nuts, seeds, which contain plenty of phenolic compounds, terpenoids, phytosterols, organosulfur exert their beneficial effect in disease prevention, by regulating several cellular molecular pathways like regulation of inflammation, redox potentials, metabolic disorder, apoptosis, and so forth . Polyphenols (flavonoids, lignans, stilbenes, etc., see Table 1) are the most diverse group of phytochemicals distributed in vegetables, fruits, olive oil, and wine and exhibit wide range of protective roles such as hypolipidemic, antioxidative, antiproliferative, and anti-inflammatory effects to reduce the onset of disease progression [3–5]. Similarly terpenoids (carotene, lycopene, etc.), another important chemically active natural hydrocarbon, contain oxygen rich moieties like alcohol, aldehydes, and ketones. Epidemiological studies have shown that the oral supplementation of tomato extract (rich in carotenoid, lycopene) significantly control the risk of hyperlipidemia, CVD, metabolic syndrome by regulating several physiological phenonmenon like reduction of blood pressure of low density lipoprotein oxidation, hypertension . Organosulfur, phytosterols are the other widely distributed active phytochemicals which have been found to reduce the generation of inflammatory signaling molecules and also modulate antioxidative effect by inhibition of NF-κB pathways [6, 7]. These phytochemicals (organosulfur, phytosterols) also show protective effect against atherosclerosis by regulating of serum total and LDL-cholesterol levels. Phytochemicals such as resveratrol, epigallocatechin gallate, gingerol, phytosterol, and myricetin directly influence various molecular signal transduction pathways like inflammation cascade, cell proliferation/migration, oxidative stress, and metabolic disorders, which are involved in the development of several noncommunicable diseases. Although beneficial effects of plant based diets or phytochemicals in reducing the risk of chronic diseases have been shown through various epidemiological and in vitro/in vivo studies, much more mechanistic and clinical evidence is required to define a particular phytochemical as an inhibitor of specific cellular pathways or identify the plant derived active compound with specific therapeutics properties. Therefore, this review is focused on the cellular targets of naturally occurring active compounds from various sources in order to explore the protective/therapeutics role as an antioxidative, anti-inflammatory regulation of metabolic disorder as well as antiproliferative properties by targeting specific molecular signal transduction, which might play a crucial role in the pathogenesis of chronic disease.
2. Bioavailability of Phytochemicals
Bioavailability of individual compounds of interest at the target site is one of the important challenges/parameters to determine the therapeutic efficiency of the target drug . Although accurate bioavailability of particular compound is not possible to predict according to Lipinski et al. a compound might have better bioavailability when it contains maximum 5 hydrogen-bond donors, and 10 hydrogen-bond acceptors, in association with having a molecular mass not more than 500 daltons; a partition coefficient log value should not be more than 5 and contains less than 10 rotatable bonds . Most of the phytochemicals, including polyphenols such as curcumin and green tea polyphenols, do not satisfy all these chemical specifications and exhibit low bioavailability . Although compounds such as genistein and biochanin A have all those good absorptive chemical properties, high rate excretion in the gut by efflux mechanism limits their bioavailability . Therefore, other factors like solubility of the compounds, stability due to gastric and colonic pH, metabolism by gut microflora, absorption across the intestinal wall, active efflux mechanism, and first-pass metabolic effects may also play crucial role in limiting the bioavailability of phytochemicals . As an example, limited bioavailability of epigallocatechin gallate is mainly due to poor absorption and rapid first-pass metabolism. Similarly low stability, increased oxidation, and high hepatic uptake are also responsible for the limited the bioavailability of some widely distributed polyphenols such as flavonoids (flavonols, anthocyanines) resveratol 8 (grapes) .
Moreover it has been also reported that rapid conjugation of a phytochemicals, especially by glucuronidation in the intestine and liver, in association with reaction of cytochrome P450 (C-P450) enzymes, which are recognized as important clearance mechanisms, is primarily responsible for their poor bioavailability . Many researchers have shown that codelivery of lead target molecules (phytochemicals) with an agent that can modulate the activity of glucuronidation or inhibit C-P450 mediated clearance mechanism is possible to increase the bioavailability of active compound of interest at the target site [12, 13]. Piperine, a component of black pepper, inhibits glucuronidation and is able to enhance the bioavailability of several bioactive compounds by altering the C-p450 mediated enzymatic biotransformation [8, 14]. Rapid mobilization in the intestine is largely responsible for low bioavailability of curcumin at target site; however consumption of curcumin along with piperin, a known inhibitor of intestinal and hepatic β-glucuronidation of curcumin, may induce the bioavailability of curcumin about 20-fold [8, 14]. Many phytochemicals were identified as promising therapeutics agent in the preliminary in vitro studies. However, when those compounds were tested into in vivo studies, many of them failed to translate the preclinical/clinical findings, because compounds either were unstable in the gut or exhibited poor bioavailability [8, 14]. Therefore, detailed preclinical and clinical studies on bioavailability of phytochemicals/active compounds are urgently needed to understand their therapeutic limitation as well as to find out the better compound delivery system to achieve the best efficiency level of the drug at the target organ.
3. Molecular Mechanism of Photochemical in Redox Modulation
Cells use enzymes and oxygen to perform its normal physiological functions are continuously exposed to free radicals. Free radicals are oxygen containing highly reactive molecules with one or more unpaired electrons. This highly reactive oxygen species (ROS) includes numerous partially reduced oxygen metabolites such as hydrogen peroxide (H2O2), hydroxyl radicals (∙OH), and superoxide anions () radicals. ROS are generated intracellularly as a byproduct of normal metabolism and as second messengers in various signal transduction pathways . ROS are also generated exogenously due to direct uptake by cells from the extracellular sources or produced during exposure of cells to some environmental triggers. It has been well established that ROS are heterogeneous and can exert their beneficial or detrimental effect depending on the concentrations at which they are present in the cellular level. At low levels, ROS can be driven by NADPH/NADPH oxidase and is required to maintain homeostatic signaling events as well as inducing cell proliferation and survival through the posttranslational modification of kinases and phosphatase . However, overproduction of ROS or exposure of cells to ROS for extended period may cause irreversible damage to DNA, protein, and lipids. Therefore, numerous innate defense systems have developed to detoxify or prevent the detrimental effect of ROS. These include nonenzymatic molecules (e.g., glutathione, vitamins A, C, and E, and flavonoids) as well as induction of phase II detoxifying/antioxidative enzymes (e.g., superoxide dismutase (SOD), catalase, and glutathione peroxidase (GSH-Px) and hemeoxygenase-1 (HO-1), which are involved to eliminate or inactivate the ROS from cellular level) . An imbalance between ROS generation and defense mechanism or inadequate presence of antioxidant molecules results in the state known as oxidative stress. Growing evidence indicates that chronic and acute excess generation of ROS under pathophysiologic conditions is pivotal in the development of cardiovascular diseases (CVD) or premature atherosclerosis progression, cancer, pulmonary fibrosis, and neurodegenerative disorder [18–20]. Oxidative modification of low density lipoprotein (Ox-LDL) regulates many signaling pathways, which causes inhibition of endothelial nitric oxide synthase (eNOS) and promotes vasoconstriction, expression of adhesion molecules, and progression of platelet aggregation. Additionally proliferation of smooth muscle cell (SMC) by Ox-LDL stimulates hypertension due to reduction of blood vessel lumen. Similarly excessive generation of ROS, particularly H2O2, has been detected in cancer cells. Though the exact sources of H2O2 generation in cancer cells are not known, the higher amount of H2O2 increases level of hydroxyl radical (OH), which in turn mediates oxidative damage of DNA and ultimately results in genomic instability. Transcriptional activation of some genes like cyclooxygenase-2 (COX-2), matrix metalloproteinases (MMPs), and cyclin B1 has been reported to be due to oxidative stress or induced generation of H2O2 [21–23]. Overexpression of these genes and H2O2 generations are also observed in breast cancer tissue, colon cancer, and cervical cancer tissue. Compelling evidence from epidemiological, clinical, and experimental studies demonstrated that phenolic and other naturally occurring compounds present in cereals, legumes, nuts, olive oil, vegetables, fruits, tea, and red wine exert antioxidative/anti-inflammatory effect through their free radical scavenging properties, as well as enhancement of antioxidative enzymes [18, 20].
Phytochemicals like curcumin, resveratrol, terpenoids, epigallocatechin-3-gallate (EGCG), and isothiocyanates share common properties and play an important role to activate the phase II detoxifying and antioxidant enzymes like HO-1, GSH-Px, and glutathione-S-transferase (GST) by targeting the common transcription factor Nrf2 [nuclear factor (erythroid derived 2) related factor] [20, 24]. Epidemiological studies reported regular consumption of lycopene (rich in tomato, spinach, etc.) significantly induced the antioxidant enzymes like SOD, GSH-Px, and glutathione reductase (GR) and reduced form of glutathione (GSH); moreover this bioactive compound also reduced the levels of lipid peroxide malondialdehyde (MDA), LDL oxidation, and ROS mediated DNA damage. Additionally, lycopene was found to induce cardioprotective effect by reducing MDA levels and increasing GSH levels in postmenopausal women [25, 26]. The redox-sensitive transcription factor Nrf2 plays an important role in regulating induction of phase II detoxifying or antioxidant enzymes (HO-1, SOD, etc.) which result in cellular defense against oxidative stress and exert cytoprotective mechanism . Many researchers have elucidated the molecular mechanisms responsible for activation of Nrf2. A cytoskeleton binding protein called Kelch-like erythroid CNC homologue- (ECH-) associated protein 1 (Keap1) binds to Nrf2 regulating its translocation to the nucleus or its activation . Following nuclear translocation, Nrf2 binds not only to the specific consensus cis-element called antioxidative responsive element (ARE) or electrophile response element (EpRE) present in the promoter region of genes encoding many antioxidant enzymes but also to other trans-acting factors such as small Maf-F/G/K as well as the coactivators of ARE including cAMP response element binding protein (CREB-binding protein or CBP), p300 that can coordinately regulate the ARE-driven antioxidant gene transcription [28–30]. Tea extract contain large amount of polyphenols (theaflavins, catechins, epicatechins, epicatechins-3-gallate, EGCG), which are characterized by 2 or more aromatic rings with at least one hydroxyl group linked by a carbon bridge. Hydroxyl group of tea polyphenols (TPs) are actually the main source for electron donor and efficiently scavenging singlet oxygen (e.g., NO, peroxynitrite). In vitro study by Leung et al. found significant reduction of oxidized LDL following application of theaflavins and catechins . Similar response was also observed by Lee et al. showing decrease in oxidized LDL in plasma of individuals after 4 weeks of green tea consumption [32, 33]. Many researchers have reported that antioxidative properties of tea polyphenols (theaflavins and catechins) might be due to inhibition of ROS-generating enzymes (e.g., iNOS), which contribute for the production of NO mediated free radicals. The molecular mechanism of antioxidant enzyme induction by EGCG or other TPs and polyphones still remain unexplored in large extent . A widely accepted model for induction of ARE-mediated antioxidant gene expression involves phosphorylation of serine/threonine residues of Nrf2 by protein kinases, leading to enhanced nuclear accumulation of Nrf2 and subsequent ARE binding. Furthermore, Wu et al. observed induction of HO-1 enzyme in endothelial cells due to activation of Akt and Nrf2 by EGCG, which impart protective measure of endothelial cell against H2O2 mediated oxidative stress . Supplementation of curcumin as well as EGCG has been reported to enhance Nrf2 nuclear translocation and upregulation of HO-1 by Akt, EKR1/2, and p38 MAPK signaling in human breast epithelial cells as wells as B lymphoblasts [27, 28, 35]. Other plausible mechanisms of EGCG-induced Nrf2 activation are oxidation or modification of cysteine thiols present in Keap1 by ROS and/or via active form of EGCG during its redox-cycling . Although EGCH mediated ARE-mediated upregulation of antioxidative gene may also be plausible through activation of MAPKs, which finally activate Nrf2. However, in contrast many studies have reported that inhibition of MAPKs by phytochemicals finally induced Nrf2 activity [27, 28]. Procyanidin B2 was found to increase nuclear translocation of Nrf2 via regulation of ERKs and p38 signaling . Similarly soy isoflavones and polyphenols rich in red wine, tea, and dark chocolate regulate vascular reactivity by targeting endothelial nitric oxide synthase (eNOS) and inducing nuclear accumulation of Nrf2. Induced endothelium-dependent NO generation in response to phytochemicals (polyphenol) may further activate cellular sensor(s) for oxidative stress and thereby enhance NO bioavailability . NO can react further with superoxide anions () to form peroxynitrite, which further upregulates nuclear accumulation of Nrf2 and activates ARE dependent transcription of phase II and antioxidant defense enzymes [37, 38]. Epidemiological studies have demonstrated that supplementation of soy isoflavones for longer period improves arterial compliance in men and postmenopausal women, induces plasma nitrite/nitrate levels, and decreases plasma endothelin-1 levels. However, in contrast, an isoflavone deficient diet fed from conception throughout adult life might result in decreased GSH concentrations and mRNA levels for eNOS. In vivo studies on aged male rats by Mahn et al. have shown that supplementation of soy protein diet rich in genistein and daidzein, found to interact with estrogen receptors, increases mRNA levels of eNOS and antioxidant enzymes . Hence, vascular protection and antioxidative effect of soy isoflavone diets mostly related to an upregulation of eNOS expression and activity, NO bioavailability in association with accumulation of Nrf2, and ARE dependent activation of antioxidant defense enzymes [37, 40]. Impaired metabolism and overproduction of ROS also contribute for neuronal degeneration and onset of neuronal diseases such as Alzheimer’s disease (AD) and Parkinson’s disease (PD). Therefore, neutralization of ROS and other types of free radicals by endogenous antioxidative enzymes (HO, GST) or regulation of oxidative stress by inducing supplementary intake of natural antioxidant is considered as a primary preventive therapeutic measure for the clinicians to protect from chronic neuronal disorder. Numerous pieces of evidence reported curcumin (rhizome of Curcuma longa), EGCG (tea), and resveratrol (grapes, berry) as potential natural occurring bioactive neuroprotective compounds because of their antioxidative properties [41, 42]. Curcumin has been shown to exert protective effect against neuronal degeneration by scavenging ROS and neutralizing NO induced free radicals. In vivo study on Alzheimer’s disease (AD) transgenic mouse model by Lim et al. demonstrated that curcumin reduces neuronal oxidative stress by inducing expression of cytoprotective proteins or antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR), glutathione peroxidase (GPx), heme oxygenase 1 (HO-1), and glutathione-S-transferase (GST) . Additionally curcumin is also able to increase the intracellular glutathione (GSH) pool by affecting the nuclear content or by triggering specific transcription factors such as 12-tetradecanoate 13-acetate (TPA), electrophilic response element (EpRE) [44, 45]. Reversal of intracellular GSH pool in AD patient by curcumin makes it unique therapeutics for AD treatment as depletion of cellular GSH level plays a pivotal role in AD pathogenesis. However because of curcumin’s low water solubility and poor bioavailability the major challenge to use curcumin as therapeutic agent for the treatment of AD is to cross the blood brain barrier (BBB) . However EGCG, main phenolic component of green tea, has been reported to have slow rate of BBB penetration and about 5% bioavailability following oral consumption . Series of rodent studies have shown the pleiotropic effect of EGCG, which exert the neuroprotective measure by modulation of antioxidative enzyme activity (SOD, GST) in association with suppression of ROS generation and protection of neuronal cells from glycation induced neurotoxicity.
Resveratrol is one of the most widely distributed phenolic compounds in fruits (apple, berry, and grapes), nuts, and so forth. Extensive study over resveratrol has shown its antioxidant properties and protective role in many chronic health issues like neural disorder (AD, PD), inflammation, CVD, and so forth. Central nervous system is one of the target organs for resveratrol as it is able to cross the BBB, although bioavailability of resveratrol is very low as it is metabolized quickly to glucuronide and sulfate conjugate. Similar to curcumin and EGCG, administration of resveratrol also mediates its neuroprotective effect via stimulation/upregulation of various antioxidant enzymatic activities such as HO, GST, and SOD. Additionally administration of resveratrol on transgenic mouse model of AD has shown protective role of this particular phytochemical against neuronal impairments mainly through inhibition of NF-κB modulated expression of several pathways like iNOS, prostaglandin E2(PGE2) [47–50]. Recent study by D’evoli et al. has shown the antioxidative and cytoprotective effects of red chicory leaf extract to improve intestinal complications are mainly due to its high content of both anthocyanins and phenolic compounds. Molecular targets of chemopreventive dietary phytochemicals are nuclear transcription factors NF-κB and hypoxia inducible transcription factor (HIF) . This finding has been further supported recently by Bak et al., who demonstrated that wild grape seed procyanidins (WGP) effectively suppressed the generation of oxidative stress mediators like ROS and nitric oxide (NO) mainly by preventing the activation of NF-κB and p38 mitogen-activated protein kinases (MAPKs) pathway in LPS-RAW264.7 cells . Bak et al. have also shown that antioxidative and chemopreventive effects of WGP are associated with induction of nuclear factor E2-related factor 2 (Nrf2)/antioxidant response element (ARE) pathway in the human hepatoma HepG2 cell line .
Induced oxidative stress and oxidative modification of LDL by ROS are one of the key risk factors for atherosclerotic plaque formation, which restricts blood flow and results in high blood pressure. Numerous phenolic/flavonoid compounds are potent inhibitors of LDL oxidation and exert their cardioprotective role by inducing antiplatelet and anti-inflammatory effects at localized (microvascular) and/or systemic level. Additionally polyphenols may also increase HDL levels and improve endothelial function. The mechanism of antioxidant activity of phenolics/flavonoid compounds can be characterized by direct scavenging or quenching of oxygen free radicals, which are mostly attributed to the o-dihydroxyl group in the A and/or B ring (catechol group) of their diphenylpropane structure . Catechol type flavonoids (e.g., quercetin, heliosin) therefore possess powerful antioxidant activity.
Human study by Aviram et al. reported small but significant (6%) decrease of lipid peroxidation in plasma following 2 wk consumption of pomegranate juice (PJ, 50 mL/day) by 13 healthy, nonsmoking men aged 20–35 years compared with plasma obtained before study entry . Additionally, a significant (9%) increase in plasma total antioxidant status was also observed after 2 wk of PJ consumption. Supplementation with 50 mL PJ/d for additional one week resulted in a further 21% decrease in plasma lipid peroxidation, whereas an additional increase in PJ supplementation to 80 mL PJ/d for another week did not inhibit plasma susceptibility to lipid peroxidation further. The inhibitory effect of PJ consumption on plasma lipid peroxidation was maintained for 2 wk after PJ supplementation ended. This study therefore showed that daily consumption of PJ may reduce the progression of atherosclerotic lesions by reducing the plasma lipid peroxidation and by virtue of its ability to attenuate platelet activations .
4. Role of Phytochemical in Inflammatory Process
Inflammation is defined as a series of immunological, biochemical, and/or cellular alterations in response to exogenous or endogenous stimuli. Both chronic and acute phase inflammatory processes act locally and systematically to activate the cells associated with inflammatory process (macrophages, endothelial cells, and fibroblast) to induce the inflammatory mediators like ROS, NO, prostaglandin E2, and proinflammatory mediators such as cytokines, TNF-alpha, and COX-2. Multiple studies have shown that overexpression of proinflammatory genes including TNF-alpha and interleukin is associated with activation of transcription factor NF-κB . Activated transcription factor translocates to the nucleus and either regulates the release of inflammatory mediators or induces the upregulation of inflammatory gene expression by binding with the DNA. Furthermore, phosphorylation of MAPK plays important role in chronic inflammation by regulating production of NO and proinflammatory genes from macrophages as well as in the activation of NF-κB [52, 56]. Hence, suppression or inhibition of those inflammatory/proinflammatory mediators is one of the major targets for treatment of many chronic diseases (cancer, CVD, and diabetes) using anti-inflammatory compounds.
Wild grapes procyanidins (WGP) induced anti-inflammatory effect and the molecular mechanism of procyanidins was studied in detail by Bak et al. using lipopolysaccharide (LPS) stimulated RAW 264.7 . In this study Bak et al. have shown that incubation of RAW 264.7 cells by WGP significantly blocked inflammatory phenomenon by reducing protein expression of iNOS and COX-2, two important inducible enzymes which play critical role in NO, PGE2 generation . Moreover, authors have shown that WGP treatment significantly reduced LPS stimulated expression of proinflammatory cytokines such as tumor necrosis factor α (TNF-α) and interleukin-1β (IL-1β) in RAW 264.7 cells. These effects of WGP might be due to suppression of nuclear factor-κB (NF-κB) activity via downregulation of MAPK and p38 pathways. Hence, suppression of NF-κB by WGP would be an important protective measure to reduce the chances of inflammation mediated chronic health issues, as transcription factor NF-κB activity plays a central role in inflammatory process . Similarly brassica derived phytochemicals like sulforaphane (SFN), phenethyl-isothiocyanate (PEITC), and indole-3-carbinol (I3C) are also found to exert anti-inflammatory effect by downregulation of LPS induced expression of COX-2, iNOS in mouse macrophages mainly by inhibiting NF-κB pathways [57–59]. In vivo study on C57BL/6 showed that pretreatment of mice with SFN resulted in significant reduction of dextran-sodium-sulfate induce colitis compared to PBS treated control mice . Similar to brassica phytochemicals, tea polyphenols, primarily EGCG, epicatechin-3-gallate (ECG), and epigallocatechin (EGC) work as chemopreventive compounds by inducing anti-inflammatory effect in cancer cells. Both EGCG and theaflavins reduced LPS-induced TNF-alpha generation and also iNOS expression by preventing activation of NF-κB [19, 61]. In vivo study by Chen et al. demonstrated that tea flower extract (TEE), rich with many polyphenols (EGCG, EGC, and ETC), possesses anti-inflammatory effect against chronic inflammation. In this study authors have shown that oral administration of TEE in mice is associated with significant reduction of tissue specific (liver) acute inflammation by blocking cytokines (TNF-alpha, IL-1β) expression and NO production . Recently increasing interest on beneficial effect of extra-virgin olive oil (EVOO) is mainly focused on the anti-inflammatory effect of phenolic compounds present in the EVOO. Glycoside oleuropein, hydroxytyrosol, and tyrosol are the major phenolic component of EVOO and have been able to inhibit inflammation by blocking eicosanoids (prostaglandin I2, Leukotriene B4) production enzymes such as COX-2, lipoxygenase (LOX), and phospholipase A2 (PLA2) in animal and human cells . Additionally, hydroxytyrosol one of the main component of EVOV reported to impart anti-coagulatory/anti-atherosclerotic effect in association with their anti-inflammatory activity in individuals with type 1 diabetic by reducing the production and accumulation of thromboxan B2 (TXB2) and hydroxyeicosatetraenoic 27 acids (HETE) in serum, which results in reduced platelet aggregation. Moreover, this particular phenolic component of EVOV can also be considered as potent anti-inflammatory agent as this is able to prevent the expression of COX-2 and iNOS in LPS-stimulated macrophages [64, 65].
Polyphenol present in red wine and black tea, for instance, quercetin, EGCG, ECG, and theflavins, are able to inhibit COX-2 and LOX in dose dependent manner following application to LPS activated murine macrophage RAW 264 cells . Likewise, kaempferol, a flavonoid widely distributed in many natural sources including apples, grapes, cabbage, and tomato, significantly reduces inflammation by inhibiting the generation of PGE2. Researchers have shown that cocoa polyphenols (flavonols, anthocyanidins, catechins, etc.) decrease the inflammation by numerous mechanisms such as inhibition of mitogen induced activation of T cells and reduced expression of IL-2 and other cytokines (IL-6, TNF-alpha). Curcumin has been identified as naturally occurring active component with wide range of medicinal effects against many chronic diseases like CVD, cancer, and metabolic disorder due to its strong antioxidative and anti-inflammatory response in vitro and in vivo. Aggarwal and Harikumar reported oral application of 70–100 mg/kg curcumin reduces systemic (plasma) and tissue specific (aortic tissue) inflammatory response as well as LDL oxidation and hypocholesteromic effects in rodents . Similarly, Nemmar et al. have shown that supplementation of curcumin as oral gavage (45 mg/kg) in male mice significantly reduces systemic inflammation by preventing the release of TNF-α and C-reactive protein (CRP) . CRP is an acute phase protein and has been identified to play an important pathogenic role in the progression of many chronic degenerative diseases like CVD, arthritis. Increased level of CRP has been observed in almost every inflammation mediated diseases onset. Similar to curcumin Pauwels et al. have shown antiarthritic/inflammatory potentials of type-A procyanidine polyphenol (TAPP) extracted from cinnamon bark. Rheumatoid arthritis (RA) is an acute inflammatory condition in joint with functional impairments mainly involved with localized (skeletal join) excessive prostaglandin synthesis as well as systemic inflammation characterized by increased level of serum CRP. Oral consumption of cinnamon bark extract and its polyphenol (procyanidine) has been found to regulate systemic inflammation by reducing CRP and was also able to stimulate autoimmune system by blocking expression of many inflammatory mediators (prostaglandin E2, NO) in RA rats . Results showed the therapeutic value of this particular polyphenol and its potential to reduce or reversal of RA progression. Due to its strong anti-inflammatory potentials TAPP is found to be successfully used to regulate airway hyperresponsiveness (AHR) or asthma by reducing inflammatory mediators like IL-4 and IL-13, which played critical role in mucus hyper-secretion and the onset of AHR . Recently Hazewindus et al. have shown synergistic effect of bioactive compounds such as lycopene, ascorbic acid, and α-tocopherol, rich in tomato. In this study authors have shown that lycopene alone significantly exerts anti-inflammatory effect by reducing the release of proinflammatory cytokine TNF-α via regulation of NF-κB activation. Moreover significant inhibition of lipid peroxidation by the combination of ascorbic acid and α-tocopherol is the complementary to the anti-inflammatory effect of lycopene.
5. Role of Phytochemicals in Metabolism Regulation
Metabolism is the cascade of cellular chemical transformation regulated by a pool of enzymes which break down the organic matter, harvest the energy (digestion), and allow the cells to grow, reproduce, and respond to molecular signal by maintaining inter- and intracellular homeostasis. Any alteration of this chain of chemical event may lead to metabolic disorder or unregulated metabolism which ultimately results in high plasma glucose level (diabetic), obesity, high blood pressure (hypertension), CVD, organ failure, and so forth. Diseases or cluster of physiological changes induced mostly by metabolic disorder like diabetes, CVD are the major health concern for morbidity with high socioeconomic burden worldwide. Modification of dietary pattern in association with regulation in life style (regular exercise, weight loss) plays an effective role to slow the deleterious effect metabolic syndrome . Epidemiological, randomized, and controlled dietary studies on human or rodents provide a lot of evidence showing that consumption of dietary fibers improves the indices of diabetes risk by regulating glycemic and plasma glucose level. The important pathogenic factors responsible for the development of metabolic disorder, insulin resistance, β-cells dysfunction, and finally diabetes are oxidative stress and tissue specific (localized) and/or systemic inflammation. Phytochemicals present in the whole grains including phytosterol, flavanols, anthocyanidins, and cinnamic acids modulate the diabetic risk by exerting their antioxidative and anti-inflammatory effect [70, 71]. Increasing number of controlled epidemiological studies has reported significant reduction of plasma cytokines (IL-6) or CRP in healthy individuals following regular consumption of rye bran and whole wheat bread. Furthermore, short-chain fatty acid of cereal fibre prevents inflammatory response in colonic mucosa by binding to the G-protein coupled receptor and also by blocking transcription factor NF-κB. Similarly consumption of brown and black rice for 4 months was found to exert cardioprotective effect by regulating oxidative stress in individuals with preexisting complications, coronary heart disease (CHD) . Although the detailed molecular mechanism is still unexplored, controlled epidemiological studies have reported the significant reduction of oxidized plasma malondialdehyde and urine prostaglandin in subjects with CHD. Similar to wholegrain, fenugreek seed and cinnamon extract has been widely used for its medicinal value in the treatment of diabetes. The hypoglycemic and hypocholesterolemic effect of fenugreek seed is mainly attributed to its high concentration of soluble fiber content, which helps to decrease the postprandial blood glucose . TAPP, the main active component of cinnamon extract significantly lowered the blood HbA1c level and also improved the insulin signaling in murine models of diabetes . Hypoglycemic effect of blueberry extract in humans is mainly due to presence of anthocyanin and myrtillin. Significant reduction of blood pressure in salt-sensitive spontaneously hypertensive rats (SHRs) supplemented with 3% blueberry enriched diet for 8 weeks might be due to vasodilator effect of blueberry polyphenol through an endothelium mediated stimulation of NO metabolism and activation of COX-induced product [74, 75]. Similarly, grape seed extract (GSE), which is a rich source of polyphenols (approximately 90% of which are procyanidins and 7% other polyphenol compounds), has become popular for the treatment and prevention of chronic cardiac disease and other disorders. In vivo studies on spontaneously hypertensive rats have shown that regular consumption of 0.5% GSE-supplemented diet significantly reduced the arterial blood pressure possible due to induction of endothelium dependent vascular dialtion . Aldolase reductase (AR), a rate limiting enzyme in polyol pathways plays an important role in the progression of diabetic complications and other chronic metabolic disorder. Detailed phytochemicals analysis by Termentzi et al. has shown Sorbus domestica fruits extract content high concentration of flavonoids and hydroxycinnamoyl esters. Further evaluation on in vitro study of Sorbus domestica fruits extract indicates high content hydroxycinnamoyl esters possess AR blocking activity. Thus regular consumption of this particular fruit extract can be the promising natural therapeutic measure for regulation of chronic or long-term diabetic complications [77, 78]. Furthermore, Russian tarragon (Artemisia dracunculus L.) extract was demonstrated to attribute antidiabetic/antihyperglycemic effect in both streptozotocin induced genetically diabetic KKAy murine models. In vitro study on hepatic cells showed that bioactive components like 6-demethoxycapillarisin and 2′,4′-dihydroxy-4-methoxydihydrochalcone are involved in hepatic glucose output by inhibiting the transcription factor for a primary enzyme, phosphoenol pyruvate carboxykinase (PEPCK) . Regular consumption of fresh bitter melon juice (popular vegetables of Asian origin) or dried whole vegetables have been found to significantly regulate the blood glucose level and diabetes-related complications including nephropathy, insulin resistance, and early cataract formation. The observed hypoglycemic effect of bitter melon might be due to presence of cucurbitane-type triterpenoids steroidal saponins called charantins, insulin-like peptides and alkaloids, which are associated with hypoglycemic activity . Similar as bitter melon, antidiabetic effect of garlic was not well documented in human studies, but garlic was found to be an effective in regulating blood glucose level in streptozotocin-induced as well as alloxan-induced diabetes mellitus in rats and mice. Although the exact mechanism of garlic as an antidiabetic agent is not clearly understood, but several in vitro studies proposed that allicin (main component of garlic) may enhance serum insulin following effective combination with cystein, or garlic can simply exert its antidiabetic effect by inducing secretion of insulin from the pancreatic beta cells or its release from bound insulin [80, 81]. However, cardioprotective role of garlic has been well documented both in vivo and controlled human studies mainly by regulation of metabolism and due to its anti-atherosclerotic effect. Many in vivo studies reported supplementation of 1–4% garlic and garlic protein diet in hypercholesterolemic rats significantly reduced serum cholesterol, triglyceride, and LDL cholesterol. Similarly, controlled human studies have shown that a dose of 4 grams of garlic cloves per day, 6 days a week for 6 months, significantly affects the LDL-C or other plasma lipid concentrations in adults (30–65 years) with moderate hypercholesterolemia . Garlic extract contains high levels of water soluble phytochemicals such as S-allyl-cystein (SAC) as well as small amount of oil soluble compounds . In vitro studies further demonstrated that this cholesterol-lowering effect of garlic might be because garlic triggers the formation of allicin through action of alliinase enzymes and allicin inhibits cholesterol synthesis in vitro [83, 84]. Even in vitro studies reveled that antiatherosclerotic and antiatherogenic activities of garlic are due to reduction of lipid content and/or LDL oxidations by allicin and SAC present in the garlic extract . Moreover, antihypertensive effect of garlic extract was also evaluated both in hypertensive rats and in controlled human (hypertensive) studies. The gamma-glutamylcysteine component of garlic might be responsible for lowering blood pressure by inhibiting angiotensin-converting enzyme in vitro [14, 80, 85]. Similar to organosulfur compound in garlic, phytosterols (including sitosterol, campesterol, and stanols) are also efficiently inducing cholesterol lowering effect both in animal and in human studies. The primary sources of phytosterols are vegetables, nuts, fruits seeds, and vegetable oil (olive oil, canola oil). Sitosterol and campesterol are the most frequent plant sterols and constitute about 60% and 35%, respectively, of plant sterols in food . Phytosterols and cholesterol are structurally similar but are metabolized differently. Due to their structural similarity to cholesterol, plant sterols are well studied for their ability to inhibit cholesterol absorption. In addition to their cholesterol lowering effect, plant sterols may possess antiatherosclerosis, anti-inflammation, and antioxidative activities . Pelletier et al. demonstrated that consumption of 0.7 g of soy sterols fed to 12 normocholesterolemic individuals reduced LDL cholesterol by 15.2% relative to the control . Many in vitro studies on caco-2 cells have shown that the hypocholesterolemic effect of plant stanols might be by reduced intestinal cholesterol due to structural similarity between plant stanols and cholesterol .
Phenolic compounds, namely, chlorogenic acid and ferulic acid, and a plant alkaloid, berberine, are also considered as potent antidiabetic agent with high therapeutic efficiency as well as less side effect. All these three phytochemicals are reported to enhance the uptake of 2 deoxyglucose (2DG) in time- and dose-dependent manner. Reduced glucose transporter (GLUT4) translocation along with impaired glucose transport is the major pathogenesis of diabetes progression. Treatment of L6 myoblasts with these above mentioned phytochemicals shows that chlorogenic acid and berberine significantly upregulate the expression of GLUT4 and peroxisomal proliferator-activated receptors-gamma (PPAR-γ) expression whereas treatment of L6 myoblasts with ferulic acid results in significant induction of GLUT4 and phosphoinositide-3-kinase (PI3K) gene expression. Based on this study researchers concluded that chlorogenic acid and berberine exert their antidiabetic effect or increased glucose uptake in PI3K independent manner; however increased glucose uptake with ferulic acid is highly dependent on PI3K pathway [90, 91]. Several in vivo and in vitro studies have demonstrated the synergistic effect of resveratrol, quercetin, and genistein in preventing obesity/weight gain and adipogenesis and also contribute to control multiple metabolic disorders like dyslipidemia, insulin resistance, and so forth. Hypolipidemic effect of resveratrol has been found to exert significant reduction of serum total cholesterol, triglycerides, and lipid content in hepatic tissue in high-fat diet hamster . Lagouge et al. revealed that the protecting activity of resveratrol on regulation of metabolism is mainly achieved due to enhancement of sirtuin 1 (Sirt1), a NAD+-dependent deacetylase activity, which improving the cellular insulin sensitivity. Therefore, consumption of plant based diet imparts beneficial effect by preventing the development and progression of age chronic diseases that are highly associated with metabolic disorder .
6. Role of Phytochemicals in Cell Migration and Proliferation
Abnormal proliferation and migration of vascular smooth muscle cells (VSMC) are the primary event contributing to the pathogenesis of atherosclerosis or restenosis and is also linked with other cellular process such as localized inflammation, arterial hypertension due to narrowing of blood vessel. Similarly excessive cell proliferation and impaired programmed cell death or apoptosis represent major causative factors for the development and progression of cancer . Therefore, this particular event is considered as a main target for the reversal of the neovascularization mediated health effect (atherosclerosis, cancer, etc.). Series of in vitro and in vivo studies has demonstrated tea as healthy beverage as it is rich source of many polyphenols (catechins, EGC, and EGCG) and is capable of reducing or slowing the progression of atherosclerosis by inhibiting the SMC proliferation and arrested the cells in G1 phase [94, 95]. EGCG is found to be effectively inducing SMC arrest by blocking cyclin D1 and cyclin E; beside this EGCG is also inhibiting the cell growth markers PCNA [94, 95]. Tea polyphenols exert antiproliferative effects by interacting also with matrix metalloproteinase (MMP) system. Expression of various MMPs has been found to be upregulated mostly in any type of cancer cells. Many studies have already shown that MMP transcription is induced and regulated by many regulators like cytokines, growth factor, ROS, and so forth. Several MMPs have been found to be as key agonists in tumor invasion, metastasis, and angiogenesis, including MMPs 1, 2, 3, 9, and 14 [96–98]. Two particular subtypes of this family, MMP 2 and MMP 9, are found to be actively involved in the turnover of basement membrane collagen and alteration of matrix proteins during angiogenesis and also plays important role for tissue remodeling. Both catechins and EGCG reduce MMP2/MMP-9 secretion in VSMC by preventing NfKB and AP-1 activities . Khan et al. have reported administration of green tea polyphenol (e.g., EGCG) in transgenic adenocarcinoma mice results in significant inhibition of cancer progression or metastasis of prostrate tissue by regulating MMP 2 and MMP 9 expression . Additionally it has been shown that both catechins and EGCG suppress PDGF-BB induced activation of PDGF-receptor mediated signal transduction pathways in VSMC by blocking tyrosine phosphorylation and their downstream molecular targets . These findings are consistent with our recent study on antiproliferative effect of Gentiana lutea and its main constituent isovitexin where Kesavan et al. have reported aqueous root extract of G. lutea and isovitexin significantly inhibit PDGF-BB induced proliferation of SMC by downregulation of ERK1/2 and iNOS expression . Similarly in another study we have shown significant antiproliferative effect of ellagic acid (EA), phenolic compound present mainly in barriers, which might be due to prevention of PDGF-BB receptor tyrosine phosphorylation/activation, reduced ROS generation, and downstream stimulation of ERK1/2 . In this study authors have also demonstrated that treatment of streptozotocin-induced diabetic rats with EA reduced the onset of atheroma formation by blocking SMC proliferation and downregulation of cyclin D1 expression . Hence all these findings suggest that regular consumption of phytochemicals is associated with prevention of cardiovascular complications. Antiproliferative effect of phytochemicals are not only inhabit the onset of CVD progressionbut also plays a significant role in cancer prevention. Curcumin and its derivatives have been found to inhibit the proliferation of breast cancer (BC) cell lines and by downregulation of matrix metalloproteinase-1 (MMP-1) expression . Resveratrol is also effectively preventing cell proliferation by stimulating cell cycle arrest via regulation of cell cycle proteins such as cyclins E and D1. Furthermore, resveratrol induces apoptosis by controlling series of events including upregulation of tumor suppressor genes p21Cip1/WAF1, p53, the proapoptotic protein Bax expression, activating caspase apoptotic signals, and downregulation of antiapoptotic proteins Bcl-2, Bcl-XL, and survivin expression. Likewise, quercetin may also act as a plant derived anticancer drug by upregulating expression of Bax, which finally leads to cell apoptosis and is able to impart antiproliferative effect by suppression of Bcl-2 protein activity and stimulation of DNA fragmentation procedure [103, 104]. Many studies reported that antimetastatic effects of phytochemicals are mainly due to alteration of activity or expression of cell adhesion molecules (CD44), which are significantly upregulated during metastasis and primarily contribute to the cancer cell growth. Ouhtit et al. have shown that treatment of BC cell line with cocktail of six phytochemicals (indole-3-carbinol, resveratrol, genistein and curcumin, C-phycocyanin, quercetin) caused a marked inhibition of proliferation and motility of cells in combination with suppression of cell adhesion molecule CD44 expression, which plays an important role as a metastasis initiating factor .
7. Role of Phytochemicals in Angiogenesis
Angiogenesis is a complex controlled phenomenon for growth and development with proangiogenic and antiangiogenenic factors. Angiogenesis is well orchestrated physiological balance between the stimulatory and inhibitory signals for new blood vessels development or preexisting vasculature. Any alteration in normal angiogenesis results in either poor vascularisation or abnormal vasculature. Chronic ischemic wound is the result of insufficient blood vessel formation or reduced angiogenesis. In contrast cancer cells or tumors induced uncontrolled angiogenesis or abnormal blood vessel growth to spread metastasis by secreting proangiogenic factors like vascular endothelial growth factors (VEGF). In a very recent work Kowshik et al. have demonstrated antiangiogenic effects of ellagic acid in a hamster model of oral oncogenesis by examining the transcript and protein expression of hypoxia-induced VEGF signaling cascade. In this study authors have found ellagic acid significantly inhibiting angiogenesis in hamster buccal punch maybe by abolishing phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K/Akt) and MAPK and VEGF signaling pathways, which involves suppression of histone deacetylase 6 (HDAC6) and hypoxia-inducible factor 1-alpha (HIF-1α) responses . Wound healing capacity of Tephrosia purpurea was studied by Lodhi et al. in rats with three different types of wound such as incision wound, excision wound, and dead space wound. Histopathological study following treatment of wound area with T. purpurea ethanolic extract has shown significant increase in angiogenesis or blood vessels formation, fibroblast cells, and collagen fibres generation due to presence of large amount of flavonoids in the extract . Several in vivo and in vitro studies have shown combination of EGCG and curcumin exhibited synergistic growth inhibition of premalignant and malignant cells through the suppression of angiogenesis, cell proliferation, and upregulation of apoptosis . Similarly Kowshik et al. have reported role of astaxanthin as a cancer preventive agent by suppression of angiogenesis. Astaxanthin, which is a non-provitamin A carotenoid predominantly distributed in microalgae, fungi, plants, and sea foods, is found to inhibit the onset of tumor progression by targeting signal transducer and activator of transcription 3 (STAT3)/Janus kinase 2 (JAK-2) .
8. Summary: Future of Phytochemicals and Therapeutic Mechanism
Relationship between phytochemicals and disease prevention has been a major focus of health research for almost half a century. Epidemiological and clinical studies indicate that the risk of chronic or noncommunicable diseases is reduced by a diet rich in fruits, vegetables, and unrefined grains. Other foods such as mono- and polyunsaturated fats, brans, nuts, plant sterols, and soy proteins have all been shown to have a favorable effect on pathogenesis of CVD (e.g., lipid profile and blood pressure lowering effect), cancer, and/or neurodegeneration. The progression in the knowledge of both the disease pathomechanisms and the targeted pathways by dietary components to exert their medicinal effect may provide new avenues to develop dietary strategies to prevent and/or to treat the numerous disorders. Based on the epidemiological and/or clinical evidence, it has been found that phytochemicals and/or naturally occurring active compounds are having broad range of physiological effects, which include reduction of inflammatory cascades, oxidative stress, improved metabolic disorder, vascular homeostasis, or antiproliferation (Figure 1). However, it is still not clear whether an individual component of the diet or a combination of nutrients and dietary habits is responsible for the observed protective effects. Therefore, screening of large scale of potential beneficial molecules present in the regular diet may provide lead molecules that may be used in the future as inexpensive dietary supplements specific to disease prevention. The products being naturally occurring in the markets would be easily available for all strata of the society. This would also open up a huge possibility of herbal product based markets and scopes of employment. The area of phytochemicals and its protective effect will only grow successfully if preclinical and/or clinical research is able to integrate credible science with thorough consumer understanding, uncompromised taste, and convenience, along with awareness about the preventive role of dietary product on the development of chronic diseases.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
Swapna Upadhyay acknowledges Council for Scientific and Industrial Research (CSIR), Government of India [Reference: CSIR-SRA (13-8553A)-2012/POOL]. Madhulika Dixit acknowledges Department of Biotechnology, Government of India-sponsored Indo-EU “FUNCFOOD” project.
- K. A. Steinmetz and J. D. Potter, “Vegetables, fruit, and cancer. I. Epidemiology,” Cancer Causes and Control, vol. 2, no. 5, pp. 325–357, 1991.
- T. Maraldi, D. Vauzour, and C. Angeloni, “Dietary polyphenols and their effects on cell biochemistry and pathophysiology 2013,” Oxidative Medicine and Cellular Longevity, vol. 2014, Article ID 576363, 3 pages, 2014.
- E. M. Alissa and G. A. Ferns, “Functional foods and nutraceuticals in the primary prevention of cardiovascular diseases,” Journal of Nutrition and Metabolism, vol. 2012, Article ID 569486, 16 pages, 2012.
- T. W. George, C. Niwat, S. Waroonphan, M. H. Gordon, and J. A. Lovegrove, “Effects of chronic and acute consumption of fruit- and vegetable-puree- based drinks on vasodilation, risk factors for CVD and the response as a result of the eNOS G298T polymorphism,” Proceedings of the Nutrition Society, vol. 68, no. 2, pp. 148–161, 2009.
- R. H. Liu, “Health benefits of fruit and vegetables are from additive and synergistic combinations of phytochemicals,” The American Journal of Clinical Nutrition, vol. 78, no. 3, supplement, pp. 517S–520S, 2003.
- S. Hirai, T. Uemura, N. Mizoguchi et al., “Diosgenin attenuates inflammatory changes in the interaction between adipocytes and macrophages,” Molecular Nutrition and Food Research, vol. 54, no. 6, pp. 797–804, 2010.
- S. C. Sahu, “Dual role of organosulfur compounds in foods: a review,” Journal of Environmental Science and Health C: Environmental Carcinogenesis & Ecotoxicology Reviews, vol. 20, no. 1, pp. 61–76, 2002.
- F. Aqil, R. Munagala, J. Jeyabalan, and M. V. Vadhanam, “Bioavailability of phytochemicals and its enhancement by drug delivery systems,” Cancer Letters, vol. 334, no. 1, pp. 133–141, 2013.
- C. A. Lipinski, F. Lombardo, B. W. Dominy, and P. J. Feeney, “Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings,” Advanced Drug Delivery Reviews, vol. 46, no. 1–3, pp. 3–26, 2001.
- S. Gao and M. Hu, “Bioavailability challenges associated with development of anti-cancer phenolics,” Mini-Reviews in Medicinal Chemistry, vol. 10, no. 6, pp. 550–567, 2010.
- C. S. Yang, S. Sang, J. D. Lambert, and M.-J. Lee, “Bioavailability issues in studying the health effects of plant polyphenolic compounds,” Molecular Nutrition and Food Research, vol. 52, supplement 1, pp. S139–S151, 2008.
- C. Manach, A. Scalbert, C. Morand, C. Rémésy, and L. Jiménez, “Polyphenols: Food sources and bioavailability,” The American Journal of Clinical Nutrition, vol. 79, no. 5, pp. 727–747, 2004.
- B. Wu, K. Kulkarni, S. Basu, S. Zhang, and M. Hu, “First-pass metabolism via UDP-glucuronosyltransferase: a barrier to oral bioavailability of phenolics,” Journal of Pharmaceutical Sciences, vol. 100, no. 9, pp. 3655–3681, 2011.
- I. Rahman, S. K. Biswas, and P. A. Kirkham, “Regulation of inflammation and redox signaling by dietary polyphenols,” Biochemical Pharmacology, vol. 72, no. 11, pp. 1439–1452, 2006.
- V. J. Thannickal and B. L. Fanburg, “Reactive oxygen species in cell signaling,” American Journal of Physiology: Lung Cellular and Molecular Physiology, vol. 279, no. 6, pp. L1005–L1028, 2000.
- R. A. Cairns, I. S. Harris, and T. W. Mak, “Regulation of cancer cell metabolism,” Nature Reviews Cancer, vol. 11, no. 2, pp. 85–95, 2011.
- J. L. Martindale and N. J. Holbrook, “Cellular response to oxidative stress: signaling for suicide and survival,” Journal of Cellular Physiology, vol. 192, no. 1, pp. 1–15, 2002.
- G. Loo, “Redox-sensitive mechanisms of phytochemical-mediated inhibition of cancer cell proliferation,” The Journal of Nutritional Biochemistry, vol. 14, no. 2, pp. 64–73, 2003.
- V. Stangl, H. Dreger, K. Stangl, and M. Lorenz, “Molecular targets of tea polyphenols in the cardiovascular system,” Cardiovascular Research, vol. 73, no. 2, pp. 348–358, 2007.
- F. Tosetti, D. M. Noonan, and A. Albini, “Metabolic regulation and redox activity as mechanisms for angioprevention by dietary phytochemicals,” International Journal of Cancer, vol. 125, no. 9, pp. 1997–2003, 2009.
- M. L. Parkett, R. E. Harris, F. S. Joarder, M. S. Ross, K. P. Clausen, and F. M. Robertson, “Cyclooxygenase-2 gene expression in human breast cancer,” International Journal of Oncology, vol. 10, no. 3, pp. 503–507, 1997.
- H. Sano, Y. Kawahito, R. L. Wilder et al., “Expression of cyclooxygenase-1 and -2 in human colorectal cancer,” Cancer Research, vol. 55, no. 17, pp. 3785–3789, 1995.
- J. Westermarck and V.-M. Kähäri, “Regulation of matrix metalloproteinase expression in tumor invasion,” The FASEB Journal, vol. 13, no. 8, pp. 781–792, 1999.
- K. T. Liby, M. M. Yore, and M. B. Sporn, “Triterpenoids and rexinoids as multifunctional agents for the prevention and treatment of cancer,” Nature Reviews Cancer, vol. 7, no. 5, pp. 357–369, 2007.
- K. S. C. Bose and B. K. Agrawal, “Effect of lycopene from cooked tomatoes on serum antioxidant enzymes, lipid peroxidation rate and lipid profile in coronary heart disease,” Singapore Medical Journal, vol. 48, no. 5, pp. 415–420, 2007.
- D. V. Ratnam, D. D. Ankola, V. Bhardwaj, D. K. Sahana, and M. N. V. R. Kumar, “Role of antioxidants in prophylaxis and therapy: a pharmaceutical perspective,” Journal of Controlled Release, vol. 113, no. 3, pp. 189–207, 2006.
- J. H. Lee, T. O. Khor, L. Shu, Z.-Y. Su, F. Fuentes, and A.-N. T. Kong, “Dietary phytochemicals and cancer prevention: Nrf2 signaling, epigenetics, and cell death mechanisms in blocking cancer initiation and progression,” Pharmacology and Therapeutics, vol. 137, no. 2, pp. 153–171, 2013.
- H.-K. Na and Y.-J. Surh, “Modulation of Nrf2-mediated antioxidant and detoxifying enzyme induction by the green tea polyphenol EGCG,” Food and Chemical Toxicology, vol. 46, no. 4, pp. 1271–1278, 2008.
- S. Dhakshinamoorthy and A. K. Jaiswal, “Small Maf (MafG and MafK) proteins negatively regulate antioxidant response element-mediated expression and antioxidant induction of the NAD(P)H:quinone oxidoreductase1 gene,” Journal of Biological Chemistry, vol. 275, no. 51, pp. 40134–40141, 2000.
- G. Shen, V. Hebbar, S. Nair et al., “Regulation of Nrf2 transactivation domain activity: the differential effects of mitogen-activated protein kinase cascades and synergistic stimulatory effect of Raf and CREB-binding protein,” Journal of Biological Chemistry, vol. 279, no. 22, pp. 23052–23060, 2004.
- L. K. Leung, Y. Su, R. Chen, Z. Zhang, Y. Huang, and Z.-Y. Chen, “Theaflavins in black tea and catechins in green tea are equally effective antioxidants,” Journal of Nutrition, vol. 131, no. 9, pp. 2248–2251, 2001.
- P. V. A. Babu and D. Liu, “Green tea catechins and cardiovascular health: an update,” Current Medicinal Chemistry, vol. 15, no. 18, pp. 1840–1850, 2008.
- M.-J. Lee, Z.-Y. Wang, H. Li et al., “Analysis of plasma and urinary tea polyphenols in human subjects,” Cancer Epidemiology Biomarkers and Prevention, vol. 4, no. 4, pp. 393–399, 1995.
- C. C. Wu, M. C. Hsu, C. W. Hsieh, J. B. Lin, P. H. Lai, and B. S. Wung, “Upregulation of heme oxygenase-1 by Epigallocatechin-3-gallate via the phosphatidylinositol 3-kinase/Akt and ERK pathways,” Life Sciences, vol. 78, no. 25, pp. 2889–2897, 2006.
- C. K. Andreadi, L. M. Howells, P. A. Atherfold, and M. M. Manson, “Involvement of Nrf2, p38, B-Raf, and nuclear factor-κB, but not phosphatidylinositol 3-kinase, in induction of hemeoxygenase-1 by dietary polyphenols,” Molecular Pharmacology, vol. 69, no. 3, pp. 1033–1040, 2006.
- I. Rodríguez-Ramiro, S. Ramos, L. Bravo, L. Goya, and M. Á. Martín, “Procyanidin B2 induces Nrf2 translocation and glutathione S-transferase P1 expression via ERKs and p38-MAPK pathways and protect human colonic cells against oxidative stress,” European Journal of Nutrition, vol. 51, no. 7, pp. 881–892, 2012.
- G. E. Mann, D. J. Rowlands, F. Y. L. Li, P. de Winter, and R. C. M. Siow, “Activation of endothelial nitric oxide synthase by dietary isoflavones: role of NO in Nrf2-mediated antioxidant gene expression,” Cardiovascular Research, vol. 75, no. 2, pp. 261–274, 2007.
- T. W. Kensler, N. Wakabayashi, and S. Biswal, “Cell survival responses to environmental stresses via the Keap1-Nrf2-ARE pathway,” Annual Review of Pharmacology and Toxicology, vol. 47, pp. 89–116, 2007.
- K. Mahn, C. Borrás, G. A. Knock et al., “Dietary soy isoflavone induced increases in antioxidant and eNOS gene expression lead to improved endothelial function and reduced blood pressure in vivo,” The FASEB Journal, vol. 19, no. 12, pp. 1755–1757, 2005.
- P. Nestel, A. Fujii, and L. Zhang, “An isoflavone metabolite reduces arterial stiffness and blood pressure in overweight men and postmenopausal women,” Atherosclerosis, vol. 192, no. 1, pp. 184–189, 2007.
- K. C. Das and C. W. White, “Redox systems of the cell: possible links and implications,” Proceedings of the National Academy of Sciences of the United States of America, vol. 99, pp. 9617–9618, 2002.
- S. Davinelli, N. Sapere, D. Zella, R. Bracale, M. Intrieri, and G. Scapagnini, “Pleiotropic protective effects of phytochemicals in Alzheimer’s disease,” Oxidative Medicine and Cellular Longevity, vol. 2012, Article ID 386527, 11 pages, 2012.
- G. P. Lim, T. Chu, F. Yang, W. Beech, S. A. Frautschy, and G. M. Cole, “The curry spice curcumin reduces oxidative damage and amyloid pathology in an Alzheimer transgenic mouse,” Journal of Neuroscience, vol. 21, no. 21, pp. 8370–8377, 2001.
- D. A. Dickinson, K. E. Iles, H. Zhang, V. Blank, and H. J. Forman, “Curcumin alters EpRE and AP-1 binding complexes and elevates glutamate-cysteine ligase gene expression,” The FASEB Journal, vol. 17, no. 3, pp. 473–475, 2003.
- H. Liu, L. E. Harrell, S. Shenvi, T. Hagen, and R.-M. Liu, “Gender differences in glutathione metabolism in Alzheimer’s disease,” Journal of Neuroscience Research, vol. 79, no. 6, pp. 861–867, 2005.
- L.-C. Lin, M.-N. Wang, T.-Y. Tseng, J.-S. Sung, and T.-H. Tsai, “Pharmacokinetics of (-)-epigallocatechin-3-gallate in conscious and freely moving rats and its brain regional distribution,” Journal of Agricultural and Food Chemistry, vol. 55, no. 4, pp. 1517–1524, 2007.
- J. A. Baur, K. J. Pearson, N. L. Price et al., “Resveratrol improves health and survival of mice on a high-calorie diet,” Nature, vol. 444, no. 7117, pp. 337–342, 2006.
- J. A. Baur and D. A. Sinclair, “Therapeutic potential of resveratrol: the in vivo evidence,” Nature Reviews Drug Discovery, vol. 5, no. 6, pp. 493–506, 2006.
- D. Kim, M. D. Nguyen, M. M. Dobbin et al., “SIRT1 deacetylase protects against neurodegeneration in models for Alzheimer’s disease and amyotrophic lateral sclerosis,” The EMBO Journal, vol. 26, no. 13, pp. 3169–3179, 2007.
- Y. A. Kim, S.-Y. Lim, S.-H. Rhee et al., “Resveratrol inhibits inducible nitric oxide synthase and cyclooxygenase-2 expression in β-amyloid-treated C6 glioma cells,” International Journal of Molecular Medicine, vol. 17, no. 6, pp. 1069–1075, 2006.
- L. D’evoli, F. Morroni, G. Lombardi-Boccia et al., “Red chicory (Cichorium intybus L. cultivar) as a potential source of antioxidant anthocyanins for intestinal health,” Oxidative Medicine and Cellular Longevity, vol. 2013, Article ID 704310, 8 pages, 2013.
- M.-J. Bak, V. L. Truong, H.-S. Kang, M. Jun, and W.-S. Jeong, “Anti-inflammatory effect of procyanidins from wild grape (Vitis amurensis) seeds in LPS-induced RAW 264.7 cells,” Oxidative Medicine and Cellular Longevity, vol. 2013, Article ID 409321, 11 pages, 2013.
- J. Terao, “Dietary flavonoids as antioxidants,” Forum of Nutrition, vol. 61, pp. 87–94, 2009.
- M. Aviram, M. Rosenblat, D. Gaitini et al., “Pomegranate juice consumption for 3 years by patients with carotid artery stenosis reduces common carotid intima-media thickness, blood pressure and LDL oxidation,” Clinical Nutrition, vol. 23, no. 3, pp. 423–433, 2004.
- R. Korhonen, A. Lahti, H. Kankaanranta, and E. Moilanen, “Nitric oxide production and signaling in inflammation,” Current Drug Targets: Inflammation and Allergy, vol. 4, no. 4, pp. 471–479, 2005.
- Y. Shan, R. Zhao, W. Geng et al., “Protective effect of sulforaphane on human vascular endothelial cells against lipopolysaccharide-induced inflammatory damage,” Cardiovascular Toxicology, vol. 10, no. 2, pp. 139–145, 2010.
- E. Heiss, C. Herhaus, K. Klimo, H. Bartsch, and C. Gerhäuser, “Nuclear factor κB is a molecular target for sulforaphane-mediated anti-inflammatory mechanisms,” Journal of Biological Chemistry, vol. 276, no. 34, pp. 32008–32015, 2001.
- A. Prawan, C. L. L. Saw, T. O. Khor et al., “Anti-NF-κB and anti-inflammatory activities of synthetic isothiocyanates: effect of chemical structures and cellular signaling,” Chemico-Biological Interactions, vol. 179, no. 2-3, pp. 202–211, 2009.
- A. E. Wagner, A. M. Terschluesen, and G. Rimbach, “Health promoting effects of brassica-derived phytochemicals: from chemopreventive and anti-inflammatory activities to epigenetic regulation,” Oxidative Medicine and Cellular Longevity, vol. 2013, Article ID 964539, 12 pages, 2013.
- A. E. Wagner, O. Will, C. Sturm, S. Lipinski, P. Rosenstiel, and G. Rimbach, “DSS-induced acute colitis in C57BL/6 mice is mitigated by sulforaphane pre-treatment,” Journal of Nutritional Biochemistry, vol. 24, no. 12, pp. 2085–2091, 2013.
- Y.-L. Lin, S.-H. Tsai, S.-Y. Lin-Shiau, and C.-T. Ho, “Theaflavin-3,3’-digallate from black tea blocks the nitric oxide synthase by down-regulating the activation of NF-κB in macrophages,” European Journal of Pharmacology, vol. 367, no. 2-3, pp. 379–388, 1999.
- B.-T. Chen, W.-X. Li, R.-R. He et al., “Anti-inflammatory effects of a polyphenols-rich extract from tea (Camellia sinensis) flowers in acute and chronic mice models,” Oxidative Medicine and Cellular Longevity, vol. 2012, Article ID 537923, 7 pages, 2012.
- C. Santangelo, R. Varì, B. Scazzocchio, R. di Benedetto, C. Filesi, and R. Masella, “Polyphenols, intracellular signalling and inflammation,” Annali dell’Istituto Superiore di Sanita, vol. 43, no. 4, pp. 394–405, 2007.
- C. L. Léger, M. A. Carbonneau, F. Michel et al., “A thromboxane effect of a hydroxytyrosol-rich olive oil wastewater extract in patients with uncomplicated type 1 diabetes,” European Journal of Clinical Nutrition, vol. 59, no. 5, pp. 727–730, 2005.
- M. C. Maiuri, D. De Stefano, P. Di Meglio et al., “Hydroxytyrosol, a phenolic compound from virgin olive oil, prevents macrophage activation,” Naunyn-Schmiedeberg’s Archives of Pharmacology, vol. 371, no. 6, pp. 457–465, 2005.
- D. Ichikawa, A. Matsui, M. Imai, Y. Sonoda, and T. Kasahara, “Effect of various catechins on the IL-12p40 production by murine peritoneal macrophages and a macrophage cell line, J774.1,” Biological and Pharmaceutical Bulletin, vol. 27, no. 9, pp. 1353–1358, 2004.
- B. B. Aggarwal and K. B. Harikumar, “Potential therapeutic effects of curcumin, the anti-inflammatory agent, against neurodegenerative, cardiovascular, pulmonary, metabolic, autoimmune and neoplastic diseases,” International Journal of Biochemistry and Cell Biology, vol. 41, no. 1, pp. 40–59, 2009.
- A. Nemmar, D. Subramaniyan, and B. H. Ali, “Protective effect of curcumin on pulmonary and cardiovascular effects induced by repeated exposure to diesel exhaust particles in mice,” PLoS ONE, vol. 7, no. 6, Article ID e39554, 2012.
- R. A. Pauwels, J. C. Kips, R. A. Peleman, and M. E. van der Straeten, “The effect of endotoxin inhalation on airway responsiveness and cellular influx in rats,” American Review of Respiratory Disease, vol. 141, no. 3, pp. 540–545, 1990.
- B. L. Graf, I. Raskin, W. T. Cefalu, and D. M. Ribnicky, “Plant-derived therapeutics for the treatment of metabolic syndrome,” Current Opinion in Investigational Drugs, vol. 11, no. 10, pp. 1107–1115, 2010.
- A. García-Lafuente, E. Guillamón, A. Villares, M. A. Rostagno, and J. A. Martínez, “Flavonoids as anti-inflammatory agents: implications in cancer and cardiovascular disease,” Inflammation Research, vol. 58, no. 9, pp. 537–552, 2009.
- Y. V. Bobryshev, S. M. Cherian, S. J. Inder, and R. S. A. Lord, “Neovascular expression of VE-cadherin in human atherosclerotic arteries and its relation to intimal inflammation,” Cardiovascular Research, vol. 43, no. 4, pp. 1003–1017, 1999.
- J.-J. Dugoua, D. Seely, D. Perri et al., “From type 2 diabetes to antioxidant activity: a systematic review of the safety and efficacy of common and cassia cinnamon bark,” Canadian Journal of Physiology and Pharmacology, vol. 85, no. 9, pp. 837–847, 2007.
- A. Z. Kalea, K. Clark, D. A. Schuschke, and D. J. Klimis-Zacas, “Vascular reactivity is affected by dietary consumption of wild blueberries in the sprague-dawley rat,” Journal of Medicinal Food, vol. 12, no. 1, pp. 21–28, 2009.
- A. Z. Kalea, K. Clark, D. A. Schuschke, A. S. Kristo, and D. J. Klimis-Zacas, “Dietary enrichment with wild blueberries (Vaccinium angustifolium) affects the vascular reactivity in the aorta of young spontaneously hypertensive rats,” Journal of Nutritional Biochemistry, vol. 21, no. 1, pp. 14–22, 2010.
- N. Peng, J. T. Clark, J. Prasain, H. Kim, C. R. White, and J. M. Wyss, “Antihypertensive and cognitive effects of grape polyphenols in estrogen-depleted, female, spontaneously hypertensive rats,” The American Journal of Physiology—Regulatory Integrative and Comparative Physiology, vol. 289, no. 3, pp. R771–R775, 2005.
- A. Termentzi, P. Alexiou, V. J. Demopoulos, and E. Kokkalou, “The aldose reductase inhibitory capacity of Sorbus domestica fruit extracts depends on their phenolic content and may be useful for the control of diabetic complications,” Pharmazie, vol. 63, no. 9, pp. 693–696, 2008.
- C. Veeresham, A. R. Rao, and K. Asres, “Aldose reductase inhibitors of plant origin,” Phytotherapy Research, vol. 28, no. 3, pp. 317–333, 2014.
- D. Govorko, S. Logendra, Y. Wang et al., “Polyphenolic compounds from Artemisia dracunculus L. inhibit PEPCK gene expression and gluconeogenesis in an H4IIE hepatoma cell line,” The American Journal of Physiology—Endocrinology and Metabolism, vol. 293, no. 6, pp. E1503–E1510, 2007.
- S. K. Banerjee and S. K. Maulik, “Effect of garlic on cardiovascular disorders: a review,” Nutrition Journal, vol. 1, article 4, 2002.
- Y.-Y. Yeh and L. Liu, “Cholesterol-lowering effect of garlic extracts and organosulfur compounds: human and animal studies,” Journal of Nutrition, vol. 131, no. 3, pp. 989S–993S, 2001.
- C. D. Gardner, L. M. Chatterjee, and J. J. Carlson, “The effect of a garlic preparation on plasma lipid levels in moderately hypercholesterolemic adults,” Atherosclerosis, vol. 154, no. 1, pp. 213–220, 2001.
- R. Gebhardt and H. Beck, “Differential inhibitory effects of garlic-derived organosulfur compounds on cholesterol biosynthesis in primary rat hepatocyte cultures,” Lipids, vol. 31, no. 12, pp. 1269–1276, 1996.
- A. Sendl, G. Elbl, B. Steinke, K. Redl, W. Breu, and H. Wagner, “Comparative pharmacological investigations of Allium ursinum and Allium sativum,” Planta Medica, vol. 58, no. 1, pp. 1–7, 1992.
- K. Rahman and G. M. Lowe, “Garlic and cardiovascular disease: a critical review,” Journal of Nutrition, vol. 136, no. 3, pp. 736S–740S, 2006.
- O. Weingärtner, M. Böhm, and U. Laufs, “Controversial role of plant sterol esters in the management of hypercholesterolaemia,” European Heart Journal, vol. 30, no. 4, pp. 404–409, 2009.
- A. Berger, P. J. H. Jones, and S. S. Abumweis, “Plant sterols: factors affecting their efficacy and safety as functional food ingredients,” Lipids in Health and Disease, vol. 3, article 5, 2004.
- S. Pelletier, S. Kundrat, and C. M. Hasler, “Effects of a functional foods nutrition education program with cardiac rehabilitation patients,” Journal of Cardiopulmonary Rehabilitation, vol. 23, no. 5, pp. 334–340, 2003.
- J. Plat and R. P. Mensink, “Increased intestinal ABCA1 expression contributes to the decrease in cholesterol absorption after plant stanol consumption,” The FASEB Journal, vol. 16, no. 10, pp. 1248–1253, 2002.
- P. K. Prabhakar and M. Doble, “Synergistic effect of phytochemicals in combination with hypoglycemic drugs on glucose uptake in myotubes,” Phytomedicine, vol. 16, no. 12, pp. 1119–1126, 2009.
- P. K. Prabhakar and M. Doble, “Interaction of phytochemicals with hypoglycemic drugs on glucose uptake in L6 myotubes,” Phytomedicine, vol. 18, no. 4, pp. 285–291, 2011.
- M. González-Castejón and A. Rodriguez-Casado, “Dietary phytochemicals and their potential effects on obesity: a review,” Pharmacological Research, vol. 64, no. 5, pp. 438–455, 2011.
- M. Lagouge, C. Argmann, Z. Gerhart-Hines et al., “Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1α,” Cell, vol. 127, no. 6, pp. 1109–1122, 2006.
- K.-Y. Chyu, S. M. Babbidge, X. Zhao et al., “Differential effects of green tea-derived catechin on developing versus established atherosclerosis in apolipoprotein E-null mice,” Circulation, vol. 109, no. 20, pp. 2448–2453, 2004.
- C.-H. Kim and S.-K. Moon, “Epigallocatechin-3-gallate causes the p21/WAF1-mediated G1-phase arrest of cell cycle and inhibits matrix metalloproteinase-9 expression in TNF-α-induced vascular smooth muscle cells,” Archives of Biochemistry and Biophysics, vol. 435, no. 2, pp. 264–272, 2005.
- X. W. Cheng, M. Kuzuya, S. Kanda et al., “Epigallocatechin-3-gallate binding to MMP-2 inhibits gelatinolytic activity without influencing the attachment to extracellular matrix proteins but enhances MMP-2 binding to TIMP-2,” Archives of Biochemistry and Biophysics, vol. 415, no. 1, pp. 126–132, 2003.
- X. W. Cheng, M. Kuzuya, T. Sasaki et al., “Green tea catechins inhibit neointimal hyperplasia in a rat carotid arterial injury model by TIMP-2 overexpression,” Cardiovascular Research, vol. 62, no. 3, pp. 594–602, 2004.
- J. El Bedoui, M.-H. Oak, P. Anglard, and V. B. Schini-Kerth, “Catechins prevent vascular smooth muscle cell invasion by inhibiting MT1-MMP activity and MMP-2 expression,” Cardiovascular Research, vol. 67, no. 2, pp. 317–325, 2005.
- N. Khan, F. Afaq, M. Saleem, N. Ahmad, and H. Mukhtar, “Targeting multiple signaling pathways by green tea polyphenol (−)-epigallocatechin-3-gallate,” Cancer Research, vol. 66, no. 5, pp. 2500–2505, 2006.
- R. Kesavan, U. R. Potunuru, B. Nastasijević, T. Avaneesh, G. Joksić, and M. Dixit, “Inhibition of vascular smooth muscle cell proliferation by Gentiana lutea root extracts,” PLoS ONE, vol. 8, no. 4, Article ID e61393, 2013.
- U. P. Rani, R. Kesavan, R. Ganugula et al., “Ellagic acid inhibits PDGF-BB-induced vascular smooth muscle cell proliferation and prevents atheroma formation in streptozotocin-induced diabetic rats,” Journal of Nutritional Biochemistry, vol. 24, no. 11, pp. 1830–1839, 2013.
- A. Ouhtit, R. L. Gaur, M. Abdraboh et al., “Simultaneous inhibition of cell-cycle, proliferation, survival, metastatic pathways and induction of apoptosis in breast cancer cells by a phytochemical super-cocktail: genes that underpin its mode of action,” Journal of Cancer, vol. 4, no. 9, pp. 703–715, 2013.
- J. Duo, G.-G. Ying, G.-W. Wang, and L. Zhang, “Quercetin inhibits human breast cancer cell proliferation and induces apoptosis via Bcl-2 and Bax regulation,” Molecular Medicine Reports, vol. 5, no. 6, pp. 1453–1456, 2012.
- A. Murakami, H. Ashida, and J. Terao, “Multitargeted cancer prevention by quercetin,” Cancer Letters, vol. 269, no. 2, pp. 315–325, 2008.
- J. Kowshik, H. Giri, T. K. Kishore et al., “Ellagic acid inhibits VEGF/VEGFR2, PI3K/Akt and MAPK signaling cascades in the hamster cheek pouch carcinogenesis model,” Anti-Cancer Agents in Medicinal Chemistry, vol. 14, no. 9, pp. 1249–1260, 2014.
- S. Lodhi, R. S. Pawar, A. P. Jain, and A. K. Singhai, “Wound healing potential of Tephrosia purpurea (Linn.) Pers. in rats,” Journal of Ethnopharmacology, vol. 108, no. 2, pp. 204–210, 2006.
- J. W. Kim, A. R. M. R. Amin, and D. M. Shin, “Chemoprevention of head and neck cancer with green tea polyphenols,” Cancer Prevention Research, vol. 3, no. 8, pp. 900–909, 2010.
- J. Kowshik, A. B. Baba, H. Giri et al., “Astaxanthin inhibits JAK/STAT-3 signaling to abrogate cell proliferation, invasion and angiogenesis in a hamster model of oral cancer,” PLoS ONE, vol. 9, no. 10, Article ID e109114, 2014.
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