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Enzyme Research
Volume 2015 (2015), Article ID 594656, 11 pages
http://dx.doi.org/10.1155/2015/594656
Review Article

Modulation of Aromatase by Phytoestrogens

Department of Physiology and Developmental Biology and The Neuroscience Center, Brigham Young University, Provo, UT 84602, USA

Received 1 October 2015; Revised 31 October 2015; Accepted 17 November 2015

Academic Editor: J. Paul G. Malthouse

Copyright © 2015 Edwin D. Lephart. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

The aromatase enzyme catalyzes the conversion of androgens to estrogens in many human tissues. Estrogens are known to stimulate cellular proliferation associated with certain cancers and protect against adverse symptoms during the peri- and postmenopausal intervals. Phytoestrogens are a group of plant derived naturally occurring compounds that have chemical structures similar to estrogen. Since phytoestrogens are known to be constituents of animal/human food sources, these compounds have received increased research attention. Phytoestrogens may contribute to decreased cancer risk by the inhibition of aromatase enzyme activity and CYP19 gene expression in human tissues. This review covers (a) the aromatase enzyme (historical descriptions on function, activity, and gene characteristics), (b) phytoestrogens in their classifications and applications to human health, and (c) a chronological coverage of aromatase activity modulated by phytoestrogens from the early 1980s to 2015. In general, phytoestrogens act as aromatase inhibitors by (a) decreasing aromatase gene expression, (b) inhibiting the aromatase enzyme itself, or (c) in some cases acting at both levels of regulation. The findings presented herein are consistent with estrogen’s impact on health and phytoestrogen’s potential as anticancer treatments, but well-controlled, large-scale studies are warranted to determine the effectiveness of phytoestrogens on breast cancer and age-related diseases.

1. Introduction

The aromatase enzyme, a product of the CYP19A1 gene, catalyzes the conversion of androgens to estrogens in many human tissue sites [13]. The biosynthesis of estrogens plays a principal role in neoplastic formation, especially in women’s health [2, 3]. For breast cancer, aromatase activity and its inhibition have become a focus of treatment historically. Also, current pharmaceutical agents classified as aromatase inhibitors characterize the importance of this enzyme in steroid biosynthesis due to the potent impact of the estrogen product [2].

Phytoestrogens are a group of plant derived naturally occurring compounds that have chemical structures similar to estrogen [4, 5]. Initially, the focus on phytoestrogens examined their ability to bind mammalian estrogen receptors [6, 7]. However, other studies investigated the influence of phytoestrogens on the human aromatase enzyme where inhibition of aromatase activity has been demonstrated [4, 5, 8]. Since phytoestrogens are known to be constituents of animal and human food sources, these compounds have received increased research attention because of their potential significance and applications in human cancers and other diseases [6, 9].

The biological properties of phytoestrogens are covered in this review, for the most part, in relationship to their ability to inhibit human aromatase enzyme activity and their applications to human cancers (especially breast cancer) and other aged-related diseases. Specifically, this review will outline (a) the aromatase enzyme with brief historical descriptions about its function, activity, and gene characteristics, (b) phytoestrogens, a group of plant derived naturally occurring compounds that have reference to their classification and applications to human health, and (c) a chronological coverage of aromatase activity modulated by phytoestrogens from the early 1980s to 2015. Each section will present a brief descriptive background for each topic, followed by how each area was derived along with human applications and/or analysis for the cited studies presented.

2. Aromatase

2.1. Historical Background

The discovery of estrogens dates back to around the 1920s [2, 10]. Other investigators in the 1930s isolated estrogens from endocrine tissues along with human and animal urine samples [2, 10]. This newly discovered compound was originally termed “theelin” and was later named estrone [10]. This provided the interest to study how estrogen synthesis was accomplished. As noted in other reports, Meyer et al. and Ryan in the 1950s along with others demonstrated the conversion of androgens to estrogens by endocrine tissues [1113].

It was quickly established via animal experimentation and human diseases/disorders that estrogens induced growth or proliferation of reproductive tissues [10]. Later, Thompson and Siiteri in the 1970s showed the aromatization of androgens in human placental microsomes [14]. Also, during the 1970s, Grodin et al. reported the extraglandular aromatization of plasma androstenedione in men and women [15]. In one case, Hemsell et al. reported that the extraglandular aromatization of androgens resulted in the feminization of a prepubertal boy [16]. It was not until the 1980s that the human aromatase cytochrome P450 protein was extracted from placental microsomes [17]. Moreover, the aromatase crystal structure was not reported until 2009 [18].

Since these investigators realized very early in their studies the importance of aromatase enzyme activity on breast, ovarian, and endometrial cancers and the mechanism of gynecomastia, soon many studies examined (1) how via mechanistic biochemical (step-by-step) processes estrogen biosynthesis took place, (2) where aromatization occurred in the body, (3) much more importantly how to regulate or inhibit the aromatase enzyme, and, finally, (4) what was the molecular biology structure of aromatase and its tissue-specific expression and regulation.

2.2. The Aromatase Enzyme Reaction

The irreversible conversion of androgens to estrogens is catalyzed by the enzyme complex termed aromatase [13, 17, 19]. Notably, the C-19 sex steroids, androstenedione and testosterone, have unsaturated A-ring structures that can serve as substrates in the aromatase reaction [17, 19, 20]. Conversely, dihydrotestosterone (DHT), a potent androgen, has a saturated A-ring which cannot be aromatized [20]. The aromatase enzyme is comprised of a microsomal cytochrome P450 complex that is a product of the CYP19A1 gene that belongs to a superfamily of P450 genes [13, 17, 19]. In general, the aromatization of androgens to estrogens takes place in the endoplasmic reticulum and is classified as a mono- or mixed-function oxidase reaction [13, 17, 19, 20]. This involves three consecutive reactions: hydroxylation, oxidation, and demethylation [17]. A highly conserved heme domain of the protein forms a ligand acceptor site (with high substrate specificity) that is involved in the aromatase reaction, and both NAPDH and oxygen are required for this conversion to produce C-18 estrogens [13, 17, 19, 20].

2.3. Tissue-Specific Sites of Aromatization

In normal human tissues aromatase enzyme activity is found in gonadal tissues (testis-Leydig and Sertoli, ovary-granulosa cells, and corpus luteum), uterus, breast, prostate, epididymis, placenta, adrenal glands, liver, skin (fibroblasts and adipose), muscle (skeletal and smooth), vascular endothelium, bone, and brain (neurons and glial) references [2, 3, 17, 19, 20]. There are many articles and reviews that provide details on this topic which is beyond the scope of this review.

However, estrogen receptor alpha and/or estrogen receptor beta have been identified in all of the tissue sites listed above for aromatase, whereby the estrogen product can exert its potent sex steroid hormone actions [17]. In fact, 17β-estradiol is the most potent steroid hormone due to its powerful proliferative actions in many cellular sites and on the other hand it has protective effects in other organs and tissues, especially with aging such as osteoporosis, cardiovascular effects, and dementia in women [10, 21].

2.4. Aromatase Inhibitors

Hormone-dependent breast cancer and other endocrine disorders prompted investigators to develop potent and selective aromatase inhibitors. One approach was to target the aromatase enzyme using analogs of natural steroidal substrates in order to determine the structure/function relationship of the aromatase conversion process. In this regard, Marsh et al. examined many steroidal aromatase inhibitors that led to the discovery of 1,4,6-androstenedione and 4-hydroxyandrostenedione (4-OH-A) [22]. In fact, 4-OH-A became the first selective aromatase inhibitor for the treatment of breast cancer in the 1980s (see Figure 1) [2, 22, 23]. This avenue of research is closely related to how phytoestrogens have similar polyphenolic structures to that of 17β-estradiol and functional groups in a conformational pattern at carbon-3 and carbon-17 analogous to that of estrogens (see Figure 1) [46].

Figure 1: The chemical structure of 17β-estradiol, the most potent sex steroid hormone in the body, with carbon-3 indicated by ● and carbon-17 indicated by ▲, displays the functional groups associated with its biological activity; 4-hydroxyandrostenedione, one of the first aromatase inhibitors used in clinical trials; genistein, a phytoestrogen of the isoflavonoid class, and; anastrozole, a current pharmaceutical agent used as an aromatase inhibitor.

A second approach, based upon known endocrine interrelationships, was to block adrenal chemical messenger (steroid) function in order to treat breast cancer [2]. This latter approach led to the accidental finding that nonsteroidal P450 inhibitors were nonselective in the inhibition of aromatase but provided some therapeutic health benefit [2]. Ultimately, these studies lead to the utilization of aromatase inhibitors as highly effective treatments for breast cancer and reproductive disorders. Some of the current pharmaceutical aromatase inhibitors include anastrozole (see Figure 1), exemestane, and letrozole [21].

Also, aromatase activity has been shown to be regulated by phosphorylation, serine/threonine kinase inhibitors, protein kinase C inhibitors, tyrosine kinase inhibitors, and other steroidal hormones and agents that influence the second messenger pathway via cyclic AMP and other pathways [2, 17, 19].

In this review the main focus will be on how phytoestrogens, such as flavonoids, lignans, and other polyphenolic molecules, alter aromatase activity in relationship to cancer. However, other topics will also be considered where the implementation of plant estrogenic compounds may serve as treatment not only for cancer but also for other endocrine and age-related diseases.

2.5. Aromatase Gene Characteristics

This topic has been the subject of several reviews [2, 17, 19, 24] and will be presented here in brief. Aromatase is encoded by the CYP19A1 gene and there is no evidence for more than one isoform of aromatase existing in the human genome [17, 19, 24]. The human CYP19A1 gene is located on chromosome 15q21.1, which consists of nine coding exons (II to X) and a 5′-untranslated region forming an approximate length of 123 kb [17, 19]. To date, 11 tissue-specific promoters have been characterized that drive aromatase expression, where promoters 1.4, 1.7, 1.3, and II are associated with breast cancer [17]. Therefore, the expression of aromatase in humans is complex with tissue-specific promoters regulating the expression of the CYP19A1 gene. In general, in reference to breast cancer, aromatase expression is not regulated by estrogens [17]. However, there is evidence that steroids control aromatase expression in brain tissue sites along with human placental tissue [17].

3. Phytoestrogens

3.1. Classifications and Human Health Applications

Phytoestrogens represent a subclass of molecules under the polyphenol umbrella due to their chemical ring structures. Additionally, phytoestrogens denote a wide variety of compounds, which are divided into several classes, that is, hydroxybenzoic acids, hydroxycinnamic acids, anthocyanins, proanthocyanidins, flavonols, flavones, flavanols, flavanones, isoflavones, stilbenes, and lignans [25]. In higher plants, thousands of molecules have polyphenolic structures (e.g., several hydroxyl groups on aromatic rings) [26]. Polyphenols and/or phytoestrogens are secondary metabolites that are thought to be involved in protecting plants against ultraviolet radiation, aggression by pathogens, or stress-related responses such as drought [26, 27]. Several hundreds of these molecules are found in edible plants that include seeds, root, stem, leaf, and fruit portions of plants [26]. They are common micronutrients in the human diet and have been studied for their role in the prevention of cancer and cardiovascular diseases [25, 26]. Also, phytoestrogens have potential health benefits in age-related diseases and disorders due to their potent free radical scavenging properties and antioxidant activities [25, 26, 28].

Phytoestrogens are naturally occurring plant compounds, which are classified into several groups based upon their structure. The main classes include lignans, phenolic acids, flavonoids, and stilbenes [29]. Figure 2 displays the different major classes of dietary phytoestrogens with a representative name and most chemical structures for each group. Of all these groups, the stilbene resveratrol is the most high-profile polyphenol known to the general public. Following resveratrol, within the last decade or so, other polyphenols such as the flavonoids and especially isoflavonoids have a high profile in commercial food products along with the health benefits of the polyphenols found in tea (e.g., phenolic acids, flavonols, and catechins) [25, 26, 30, 31].

Figure 2: Classification and chemical structure of major classes of phytoestrogens.

Novel insights of dietary polyphenols in the prevention of human disease and improving health covering such topics as cardiovascular, obesity, and inflammation/antioxidant effects, diabetes, and dermal protection have been reported [3235].

3.2. Historical Background

Many phytoestrogens or polyphenolic compounds were discovered at about the same time as steroid hormones. For example, resveratrol, a polyphenolic stilbene, was first isolated by Takaoka in the 1940s [36]. Later Nonomura isolated resveratrol from Japanese knotweed (Pediomelum cuspidatum) in 1963 [37] with subsequent studies demonstrating that resveratrol was found in red grapes (wine) in 1992 by Siemann and Creasy [38]. Later, Bertelli et al., in 1995, reported that resveratrol had some cardioprotective effects [39]. However, there has been a dramatic increase in the number of journal articles about resveratrol since the discovery of its chemoprotective effects by John Pezzuto’s laboratory in early 1997 [40]. This report showed the potential of resveratrol to prevent tumor initiation, promotion, and progression which may be used as a potential anticancer agent [41]. The publication history of resveratrol since this important discovery has shown a number of publications on the beneficial effects of resveratrol and calorie restriction, including the “French paradox,” where the abundant levels of resveratrol in red wines may be responsible for the surprisingly normal lifespan of the French in spite of their heavy consumption of fatty foods that can cause heart disease [41]. In addition to red grapes (wine), many other food products have been shown to contain natural resveratrol [41, 42].

Subsequent to the discovery by Pezzuto’s laboratory on resveratrol’s chemopreventive effects, more recent investigations during the last decade have focused on the mechanisms of how resveratrol acts especially in cell signaling paradigms covering cancer prevention, cardiovascular, and antiobesity along with its antioxidant and anti-inflammatory effects [4143]. For example, resveratrol treatment not only covered cardiovascular protective actions but also alleviated diabetes-induced cardiovascular disorders via different endogenous signaling pathways including oxidative stress and glucose and insulin metabolism [44] as well as antidiabetic actions [45, 46]. In fact, a recent review by Park and Pezzuto in 2015 demonstrates the importance of resveratrol’s pharmacological effects over the past five years (2009–2014) and covers a variety of research topics including cardiovascular, inflammation, carcinogenesis, the aging process, diabetes, neurological dysfunction, prostate, skin, and other disorders and diseases [47].

Other examples of the isoflavonoid class include daidzein, genistein, and equol. Equol was first isolated in 1932 and then identified approximately 50 years later in human urine as metabolite of the soy isoflavone daidzein [48]. These aglycones act like natural selective estrogen receptor modulators (SERMs) at various tissue sites throughout the body [48, 49]. Early on genistein received a great deal of research attention in the 1980s and throughout the 1990s due to its abundance and ready detection and quantification [49]. It was not until the equol hypothesis was proposed in the late 1990s that a shift in research focus was made toward equol [48]. Notably, the equol hypothesis suggests that the generation or consumption of equol above arbitrary threshold levels impacts health benefits for various disorders or diseases [48, 49]. Since this transition interval, there has been a dramatic increase in research publications on equol [48, 49].

Equol has many of the health benefits that are comparable to resveratrol, although equol, unlike its precursor daidzein (or genistein), is unique in having a chiral carbon at position C-3 of the pyran ring [48, 49]. It therefore can occur as two distinct isomers as S-equol or R-equol. Notably both isomers have unique antiandrogenic properties where they both specifically bind 5α-dihydrotestosterone (5α-DHT) [49, 50]. Equol is also a superior antioxidant, having greater antioxidant capacity than vitamin C or vitamin E [49], and it has many other benefits covering cosmetics, prostate, and breast cancer along with several other health applications [4852].

Finally, it is not surprising that these phytoestrogens not only act as SERMs but also have the ability to alter the activity of the aromatase enzyme. Thus, the next sections deal with a brief historical coverage starting in the 1980s to 1999 followed by publications from 2000 up until 2014 of how various phytoestrogen compounds inhibit aromatase enzyme activity especially with regard to cancer. However, with the advancements in technology, the 2000 to 2014 interval displays a complex, evolving scientific investigative story.

3.3. 1980s–1999: Phytoestrogen Modulation of Aromatase Activity

In the 1980s, the pioneering work of Herman Adlercreutz along with Kenneth Setchell and other investigators demonstrated that dietary sources of nonsteroidal estrogen-like compounds had a profound impact on estrogen levels in women and the potential roles these molecules may play in hormone-dependent diseases, such as breast cancer [5358]. This collective work sets up the stage for investigating how diet may influence disease such as cancer [6, 59].

One of the earliest reports on phytoestrogen compounds inhibiting aromatase activity was reported by Kellis Jr. and Vickery in 1984 who showed that several naturally occurring flavones altered estrogen biosynthesis [60] (see Table 1). Later in the late 1980s and into the 1990s, along with the development of steroid analogs as aromatase inhibitors [2, 73, 74], other investigators examined naturally occurring lignan and flavonoid compounds that inhibited aromatase activity in human preadipocytes [61, 62], human placental tissue [5, 6365], JEG-3 cells [5], and ovarian tissue in rainbow trout [63]. In the late 1990s, premenopausal women were fed soy isoflavones for approximately 100 days and urine samples were collected to quantify estrogen excretion levels [75]. This last study demonstrated that soy isoflavone consumption may exert cancer-preventive effects by decreasing estrogen synthesis presumably by altering aromatase enzyme activity based upon previously published reports [75]. Finally several synthetic flavones were found to inhibit the aromatization of androstenedione to estrone using human placental microsomes [66] (see Table 1).

Table 1: Inhibition of aromatase by phytoestrogen classification.
3.4. 2000–2014: Phytoestrogens Modulation of Aromatase Activity
3.4.1. Increased Interest in Natural Compounds

During the mid to late 1990s there was a trend for many women to turn to “natural” alternative therapies to treat perimenopausal and postmenopausal symptoms [76]. Notably, at this time interval, most women did not elect to take hormone replacement therapy (HRT) and those that did usually stopped or decreased their compliance due to the potential adverse effects of this treatment, especially in reference to cancer issues [77]. Also during this interval recall, in 1991 the women’s health initiative (WHI) started and was to run until 2005 but was stopped after an average follow-up of 5.2 years. The WHI investigators’ report was published in July of 2002 in the Journal of the American Medical Association (JAMA), which generated confusion due to the fact that the general public did not know how to understand the data [78]. In fact the safety of HRT was challenged, where estrogen plus progestin was shown to increase the risk of invasive breast cancer, coronary heart disease, stroke, and pulmonary embolism, while the risk of colorectal cancer and bone fracture was decreased [78]. This report provided a strong initiative for women to investigate in a more dramatic fashion the use of alternative therapies [76, 79]. Concurrently, Adlercreutz reported in the early 2000s that phytoestrogens had a preventive effect against various cancers and breast cancer specifically. This suggested a dietary link to increase health, in general, and potential prevention of age-related diseases, [80, 81] which supported early reports on this topic [6, 5559].

For example, during this time, it was estimated that 50% of Americans used some type of dietary supplement on a regular basis and 30 to 50% of women used a “natural” remedy during the postmenopausal interval to address their physical condition in an attempt to improve reproductive-endocrine function while at the same time avoiding the potential adverse effects associated with traditional HRT [76, 79, 82, 83]. Consequently, more women (and men) have turned to natural health remedies such as phytoestrogens (with their polyphenolic chemical structures made in plants) which has become one of the most researched topics in the last decade.

3.4.2. Screening of Natural Compounds (Structure-Function Relationships)

The advancement of technology has enabled investigators to perform what used to be labor-intensive experiments that would take weeks or days and cut the time to conduct these studies by 90% or more. In some cases like molecular and/or gene microarray studies these techniques evolved from the slow paced single compound or isolated gene examination in 1980s and 1990s into high volume and high throughput detection analysis generating pages of data in a very brief time.

For example, before the crystal structure of the aromatase enzyme was reported in 2009, some investigators used three-dimensional modeling techniques of aromatase for structure-based drug design [84]. Others used the concept that dietary phytoestrogens are defined as natural chemicals present in our diet which can mimic or modulate estrogen’s hormone action and focused on (a) isoflavones (e.g., soybeans) which constitute the largest group of isoflavonoids (via dietary sources), (b) flavonoids (where over 4,000 compounds have been identified in plant sources), (c) stilbenes, such as resveratrol, and (d) the lignans (i.e., enterolactone and enterodiol) [67]. From such studies numerous reports have confirmed the potential of flavones as aromatase inhibitors [67], such as naringenin, hesperetin, eriodictyol, and naringin. However, in general, flavones are more potent aromatase inhibitors than flavanones [85]. The isoflavonoid molecules, such as biochanin A and formononetin, are strong aromatase inhibitors, while the stilbene and lignan compounds have been shown to be weak aromatase inhibitors [67] (see Table 1).

With regard to modern techniques, Paoletta et al. [86] screened forest phytochemical compounds (constituents of 240 herbs used in traditional Chinese medicine) and identified a number of agents as potential aromatase inhibitors using molecular modeling/docking studies, and the “virtual screening” candidates were subsequently confirmed via aromatase inhibition assays. The flavones, myricetin, and gossypetin displayed inhibitory aromatase activity along with the flavanone, liquiritigenin, which was more potent compared to the aromatase inhibitor, aminoglutethimide [86].

Finally, nutrition mixtures of phytoestrogens and mycotoxins that are commonly found as food contaminants (i.e., zeranol, aflatoxin B, and zearalenone) were tested for their influence on aromatase activity [4, 87]. Taxvig et al. tested 12 food relevant phytoestrogens and found that all of the test materials increased estrogen production and decreased testosterone production, implying that aromatase activity was increased in three different cell lines [4]. Conversely, in another study, zearalenone was found to inhibit aromatase activity using four different cell lines suggesting that not only may molecules from dietary sources impact steroid biosynthesis but also food contaminants may contribute to the modulation of steroid hormone levels [87].

3.4.3. Inhibition or Stimulation of Aromatase Activity

In the 21st century investigators continued to examine phytoestrogen’s influence on aromatase but used experimental designs that focused on human breast cancer. In part, this approach was supported by previously published reports demonstrating that isoflavones and other phytoestrogens compounds had antiestrogenic, antiproliferative, and antiaromatase activities. Also, the fact that breast cancer is the predominant type of cancer in industrialized countries, the second leading cause of cancer-related deaths in women, and the increased public awareness of breast cancer campaign galvanized research efforts along this path.

In 2000 Le Bail et al. reported that many phytoestrogens compounds with a B-ring at position-2 were more potent aromatase enzyme inhibitors using human placental microsomes compared to phytochemicals with a B-ring at position-3 [88]. For example, the compounds, flavone, 7-hydroxyflavone, 7-methylflavone, 7,8-dihydroxyflavone, chrysin, apigenin, and naringenin (containing a B-ring at position-2), displayed greater aromatase enzyme inhibition compared to coumestrol, genistein, daidzein, biochanin A, and formononetin containing a B-ring at position-3 [88].

Investigators using MCF-7 cells showed that mammalian lignans (enterolactone and enterodiol) and genistein decreased aromatase enzyme activity suggesting that modulation of local estrogen synthesis is one potential mechanism through which the lignans and genistein protect against breast cancer [68]. Other investigators using human primary mammary fibroblasts and MCF-7 cocultures showed that phytochemicals inhibited aromatase enzyme activity in the following order: biochanin A > genistein > naringenin > apigenin > chrysin [69] (see Table 1). However, in this in vitro study, along with other reports, phytoestrogens were shown to increase cell proliferation at concentrations that are not uncommon in blood of individuals using food supplements [4, 8991]. Some in vitro studies reported that genistein induced aromatase enzyme activity along with cell proliferation in a breast cancer model [89, 91]. Although some reports suggested that phytoestrogens tested at higher μM concentrations may decrease cell viability, interact with estrogen receptors, and potentially alter the obtained results in reference to cellular proliferation, that resulted in no effect on aromatase enzyme activity or stimulation of aromatase gene expression [88, 92].

In reference to breast cancer, the disposition of soy isoflavones in normal breast tissue has been reported, where a dietary intervention study of healthy women consuming soy milk for 4 to 5 days before esthetic breast reduction (along with blood sample collection) was performed [93]. Genistein and daidzein serum concentrations ranged from 135 to 2831 nmol/L and from 105 to 1397 nmol/L, respectively, and from 92 to 494 pmol/g and from 22 to 771 pmol/g, respectively, in breast tissue samples. The total isoflavones showed a breast adipose/glandular tissue distribution of 40 : 60 ratio and their concentrations were approximately 30-fold higher compared to 17β-estradiol concentrations suggesting that dietary intake of soy products reached levels in breast tissue that may provide health benefits [93].

In brief, reports from human studies examining phytoestrogens provide valuable data from which a comparison can be made as to the confirmation or divergent results seen in in vitro and animal studies [49]; since the outcomes or endpoints include no change, a decrease or increase of health benefits related to exposure to phytochemicals. Several reports suggest that dietary soy isoflavone intake was associated with lower risk of occurrence and recurrence among postmenopausal patients with breast cancer positive for estrogen and progesterone receptor [9496]; the development of phytoestrogen therapy for breast cancer prevention is supported by historical and regional dietary intake patterns [5559, 80, 81] and the health benefits and the mechanisms by which these polyphenolic molecules exert their positive effects have been reviewed [97101].

3.4.4. Alteration in Aromatase mRNA Levels

In addition to examining aromatase enzyme activity, some reports have shown that phytoestrogens inhibit aromatase mRNA expression. Rice et al. in 2006 showed that the flavones, apigenin and quercetin, and the isoflavones, genistein, daidzein, and biochanin A, displayed dose-dependent reductions in aromatase mRNA levels with apigenin as the most potent inhibitor of aromatase [70]. Additionally low dose (0.1 μM to 10 μM) combinations of the phytoestrogens were also effective in the reduction of aromatase mRNA levels using human ovarian tissue [70] (see Table 1).

Chi et al. showed that the red clover isoflavone, biochanin A, also inhibits aromatase activity and mRNA expression using breast cancer cell lines (MCF-7 and SK-BR-3) and implicated that the transcriptional control of the CYP19 gene is exon-specific [96]. In addition to biochanin A, the phytoestrogen, genistein, since it did not inhibit aromatase activity but did suppress CYP19A1 gene expression via promoters 1.3 and II, suggested another mechanism by which local estrogen biosynthesis may be regulated [71] (see Table 1). Also examining aromatase promoter mechanisms Wang et al. showed that the food contaminants, zearalenone and zeranol, suppressed aromatase expression through promoters II and 1.3, with zearalenone being the most potent aromatase inhibitor [87]. In investigating other biochemicals, the compound extracted from the tree Ginkgo biloba displayed aromatase inhibitory effects at both the enzyme (JEG-3 cells) and CYP19A1 expression levels [102]. This study also examined specific promoter CYP19A1 sequences in recombinant microsomes, which suggested a dose-dependent decline in aromatase gene expression that may have potential applications to breast cancer [102]. Celik et al. tested several vegetables (Laurus nobilis, Mentha piperita, Crocus sativus, and Allium) as potential aromatase inhibitors via mRNA expression in human non-small cell lung cancer cell lines and found that all were effective CYP19A1 inhibitors presenting a potential role and mechanism of action, where foods may reduce the risk of certain cancers [103]. Conversely, Ye et al. reported that the isoflavone, genistein, induced aromatase activity and increased aromatase mRNA expression in hepatic cells (HepG2) with the concurrent utilization of the CYP19A1 promoters 1.3 and II [104]. Finally, Khan et al. have reviewed studies examining phytochemicals and the potential utility of natural products as regulators of aromatase promoters as therapeutic agents against breast cancer [72] (see Table 1).

4. Summary

The importance of the aromatase enzyme (CYP19A1 gene) to catalyze the conversion of androgens to estrogens in many human tissue sites that are known to stimulate cellular proliferation in breast cancer represents one of the most crucial health issues of our time. Naturally occurring compounds derived from plants which have chemical structures similar to estrogen are classified as phytoestrogens and have received increased research attention because of their potential significance/application in human cancers and other diseases. The inhibition of aromatase (enzyme activity and gene expression) represents one key mechanism of how phytoestrogens may contribute to decreased cancer risk and recurrence (see Figure 3). In general, phytoestrogens act as aromatase inhibitors by (a) decreasing aromatase gene expression (by reducing promoter utilization), (b) inhibiting the aromatase enzyme itself, or (c) in some cases acting at both levels of regulation to diminish local estrogen biosynthesis and cellular proliferation. The findings presented herein are consistent with estrogen’s impact on health and phytoestrogens’ potential as anticancer agents as well as treatments for other diseases, but well-controlled, large-scale studies are warranted to determine the effectiveness of phytoestrogens on breast cancer and age-related diseases.

Figure 3: Mechanisms of aromatase inhibition (gene expression and enzyme activity) by phytoestrogens.

Conflict of Interests

The author declares that there is no conflict of interests regarding the publication of this paper.

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