Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 6374940 | https://doi.org/10.1155/2019/6374940

Frederik Roos, Katherina Binder, Jochen Rutz, Sebastian Maxeiner, August Bernd, Stefan Kippenberger, Nadja Zöller, Felix K.-H. Chun, Eva Juengel, Roman A. Blaheta, "The Antitumor Effect of Curcumin in Urothelial Cancer Cells Is Enhanced by Light Exposure In Vitro", Evidence-Based Complementary and Alternative Medicine, vol. 2019, Article ID 6374940, 8 pages, 2019. https://doi.org/10.1155/2019/6374940

The Antitumor Effect of Curcumin in Urothelial Cancer Cells Is Enhanced by Light Exposure In Vitro

Academic Editor: Francisco Solano
Received09 Nov 2018
Revised15 Feb 2019
Accepted25 Feb 2019
Published11 Mar 2019

Abstract

The natural compound curcumin exerts antitumor properties in vitro, but its clinical application is limited due to low bioavailability. Light exposure in skin and skin cancer cells has been shown to improve curcumin bioavailability; thus, the object of this investigation was to determine whether light exposure might also enhance curcumin efficacy in bladder cancer cell lines. RT112, UMUC3, and TCCSUP cells were preincubated with low curcumin concentrations (0.1-0.4 μg/ml) and then exposed to 1.65 J/cm2 visible light for 5 min. Cell growth, cell proliferation, apoptosis, cell cycle progression, and cell cycle regulating proteins along with acetylation of histone H3 and H4 were investigated. Though curcumin alone did not alter cell proliferation or apoptosis, tumor cell growth and proliferation were strongly blocked when curcumin was combined with visible light. Curcumin-light caused the bladder cancer cells to become arrested in different cell phases: G0/G1 for RT112, G2/M for TCCSUP, and G2/M- and S-phase for UMUC3. Proteins of the Cdk-cyclin axis were diminished in RT112 after application of 0.1 and 0.4 μg/ml curcumin. Cell cycling proteins were upregulated in TCCSUP and UMUC3 in the presence of 0.1 μg/ml curcumin-light but were partially downregulated with 0.4 μg/ml curcumin. 0.4 μg/ml (but not 0.1 μg/ml) curcumin-light also evoked late apoptosis in TCCSUP and UMUC3 cells. H3 and H4 acetylation was found in UMUC3 cells treated with 0.4 μg/ml curcumin alone or with 0.1 μg/ml curcumin-light, pointing to an epigenetic mechanism. Light exposure enhanced the antitumor potential of curcumin on bladder cancer cells but by different molecular action modes in the different cell lines. Further studies are necessary to evaluate whether intravesical curcumin application, combined with visible light, might become an innovative tool in combating bladder cancer.

1. Introduction

Bladder cancer is the second most common urological cancer in Europe and North America [1], whereby transitional cell carcinoma (TCC) accounts for >90% of these patients [2]. The majority of TCC (>70%) is a nonmuscle-invasive bladder cancer (NMIBC), confined to the bladder mucosa and lamina propia, staged as pTa or pT1 tumors. Standard treatment for NMIBC is transurethral resection (TUR), but the risk of recurrence (60–70%) due to reattachment of released tumor cells is high [3]. To prevent tumor recurrence following TUR, intravesical instillation therapy with chemotherapeutic drugs such as mitomycin has been employed [4, 5]. Due to a higher efficacy against pT1 and pTcis TCC, intravesical bacillus Calmette-Guerin (BCG) immunotherapy has become the treatment of choice over the past three decades. However, cystitis and systemic toxicity are serious side effects [2]. Furthermore, a number of patients suffering from TCC are resistant to conventional intravesical therapy, necessitating the development of less toxic, but effective drugs to combat the disease.

The use of nutraceuticals and functional foods as an alternative or complementary (CAM) option for the prevention and treatment of human disease has gained high popularity. Indeed, natural products play an indispensable role as drugs, supplements, and lead compounds for patients suffering from cancer. About 50% of patients applying CAM-methods employ natural herbs [68], either to boost the immune system, to actively contribute to the tumor therapy, and/or to lower the risk of cancer relapse [9].

Still, though natural plant products are well accepted and their application rates high, scientifically based information about their antitumor efficacy is sparse and the herbal compound curcumin is no exception. Curcumin is a polyphenolic substance extracted from the rhizome of Curcuma longa, commonly known as turmeric [10]. Several studies have confirmed that curcumin induces various pharmacological-biological processes, including cell cycle arrest and modulation of cell cycle regulating proteins, along with the induction of apoptosis and suppression of tumor promoting transcription factors [11]. Curcumin also blocks crucial steps of metastasis by altering adhesion molecules involved in metastatic tumor progression [12]. Animal and human studies have shown that curcumin is safe and well tolerated, even when highly dosed [1316].

Conveying curcumin from the bench to the bedside is challenging, since the compound is poorly absorbed and improperly metabolized, resulting in poor bioavailability. Hence, strategies must be developed to enhance the bioavailability of curcumin and open the way to clinical application. Visible and UVA light have recently been shown to amplify the growth blocking potential of curcumin in cell culture and animal studies [17, 18] and curcumin has proven highly effective in treating psoriatic patients, when activated with light phototherapy [19]. Little is known about the antitumor potential of curcumin in TCC and light activation could exert an effect here as well. Therefore, the effect of curcumin on growth and proliferation of different urothelial cancer cells was investigated to elucidate underlying signal transduction pathways.

2. Materials and Methods

2.1. Cell Culture

RT112, UMUC3 (ATCC/LGC Promochem GmbH, Wesel, Germany) and TCCSUP (DSMZ, Braunschweig, Germany) bladder carcinoma cells were grown and cultured in RPMI 1640 supplemented with 10% fetal calf serum (FCS), 20 mmol HEPES buffer, 1% glutamax and 1% penicillin/streptomycin (all: Gibco/Invitrogen; Karlsruhe, Germany) in a humidified, 5% CO2 incubator. RT112 is an invasive (pathological stage T2) moderately differentiated (grade 2/3) model of human bladder cancer, UMUC3 a high grade 3 invasive bladder cancer. TCCSUP represents a transitional cell carcinoma, grade 4. Subcultures from passages 7–24 were selected for experimental use.

2.2. Curcumin and Light Exposure

Curcumin (Sigma Aldrich, Taufkirchen, Germany) was stored at -20°C and was diluted in cell culture medium to either 0.1, 0.2, or 0.4 μg/ml final concentration prior to use. Tumor cells were treated with curcumin for 1 h. Subsequently, RPMI based cell medium was replaced by phenol red free phosphate buffered saline (PBS) with Ca2+/Mg2+ (Gibco/Invitrogen) and subjected to visible light exposure (5500 lx, 1.65 J/cm2; Waldmann UV 801AL, Villingen-Schwenningen, Germany) for 5 min. After irradiation PBS was replaced by cell culture medium containing no curcumin. Controls were cell cultures exposed to visible light without curcumin, exposed to curcumin without light exposure, or treated with PBS alone. Tumor cells were then subjected to the assays listed below.

2.3. Cell Growth, Proliferation, and Apoptosis

We followed the methods of Juengel et al. [20]. Cell growth was assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) dye reduction assay (Roche Diagnostics, Penzberg, Germany). Bladder cancer cells (50 μl, 1 × 105 cells/ml) were seeded onto 96-well tissue culture plates. After 24, 48, and 72 h, 10 μl MTT (0.5 mg/ml) were added for an additional 4 h. Thereafter, cells were lysed in a buffer containing 10% SDS in 0.01 M HCl. The plates were incubated overnight at 37°C, 5% CO2. Absorbance at 550 nm was determined for each well using a microplate enzyme-linked immunosorbent assay (ELISA, Tecan Infinite M200, Männedorf, Switzerland) reader. After subtracting background absorbance, results were expressed as mean cell number.

Cell proliferation was measured using a BrdU cell proliferation enzyme-linked immunosorbent assay (ELISA) kit (Calbiochem/Merck Biosciences, Darmstadt, Germany). Tumor cells (50 μl, 1 × 105 cells/ml), seeded onto 96-well plates, were incubated with 20 μl BrdU-labeling solution per well for 8 h, fixed and detected using anti-BrdU mAb according to the manufacturer’s instructions. Absorbance was measured at 450 nm using a microplate ELISA reader.

To evaluate whether tumor cell growth was impaired or reduced due to apoptosis, the expression of Annexin V/propidium iodide (PI) was evaluated using the Annexin V-FITC Apoptosis Detection kit (BD Pharmingen, Heidelberg, Germany). Tumor cells were washed twice with PBS and then incubated with 5 μl of Annexin V-FITC and 5 μl of PI in the dark for 15 min at RT. Cells were analyzed by flow cytometry using FACScalibur (BD Biosciences, Heidelberg, Germany). The percentage of apoptotic (early and late), necrotic, and vital cells in each quadrant was calculated using CellQuest software (BD Biosciences).

2.4. Cell Cycling

Cell cycle analysis was carried out on subconfluent cell cultures. Tumor cell populations were stained with PI, using a Cycle TEST PLUS DNA Reagent Kit (Becton Dickinson, Heidelberg, Germany) and then subjected to flow cytometry using FACScan (Becton Dickinson). 10,000 events were collected from each sample. Data acquisition was carried out using CellQuest software and cell cycle distribution was calculated using the ModFit software (Becton Dickinson). The number of gated cells in the G1, G2/M, or S-phase was expressed as % [20].

2.5. Cell Cycle Regulating Proteins

Cell cycle regulating proteins were investigated by Western blot. Tumor cell lysates were applied to a 7%–15% polyacrylamide gel (depending on protein size) and electrophoresed for 90 min at 100 V. The protein was then transferred to nitrocellulose membranes (1 h, 100 V). After blocking with nonfat dry milk for 1 h, the membranes were incubated overnight with monoclonal antibodies directed against the following cell cycle proteins, all from BD Biosciences, Heidelberg, Germany, if not otherwise indicated: Cdk1 (IgG1, clone 1, dilution 1:2,500), phospho-Cdk1 (pTyr15; IgG1, clone 44), cdk2 (IgG2a, clone 55, dilution 1:2,500), phospho-Cdk2 (Thr160; MerckMillipore, Darmstadt, Germany), cyclin A (IgG1, clone 25, dilution 1:250), cyclin B (IgG1, clone 18, dilution 1:1,000), cyclin D1 (IgG1, clone G124-326, dilution 1:250), Skp1 p19 (IgG1, clone 52/p19, dilution 1:5,000), and p27 (IgG1, clone 57, dilution 1:500).

To investigate histone acetylation, cell lysates were marked with antiacetylated histone H3 (rabbit IgG, clone Y28, dilution 1:500, Epitomics, USA) and antiacetylated histone H4 (Lys8, rabbit IgG, dilution 1:500, Upstate Biotechnology, USA).

HRP-conjugated goat anti-mouse IgG (Upstate Biotechnology, Lake Placid, NY, USA; dilution 1:5,000) served as the secondary antibody. The membranes were briefly incubated with ECL detection reagent (ECLTM, Amersham/GE Healthcare, Munich, Germany) to visualize the proteins and then were analyzed by the Fusion FX7 system (Peqlab, Erlangen, Germany). ß-actin (1:1,000; Sigma Aldrich) served as internal control.

Gimp 2.8 software was used to perform pixel density analysis of the protein bands. The ratio of protein intensity/β-actin intensity was calculated and expressed in percentage, related to controls set to 100%.

2.6. Statistics

All experiments were performed three to six times. Statistical significance was calculated with the Wilcoxon–Mann-Whitney U test. Differences were considered statistically significant at a P value less than .05.

3. Results

3.1. Effect of Curcumin on Tumor Cell Growth and Proliferation

Curcumin alone, added at a concentration from 0.1 to 0.4 μg/ml, did not alter cell growth of RT112 cells, slightly reduced UMUC3 cell growth at 0.4 μg/ml, and only moderately suppressed growth of TCCSUP at 0.2 and 0.4 μg/ml, each compared to respective controls (Figure 1). When RT112 cells were exposed to visible light, curcumin efficacy was considerably enhanced. The same effect was seen with UMUC3 and TCCSUP cells, with a complete growth blockade at 0.4 μg/ml (UMUC3) or already at 0.2 μg/ml (TCCSUP) (Figure 1). Light alone did not influence tumor cell growth (data not shown).

The BrdU incorporation assay revealed no change in BrdU uptake in cells not treated with visible light, independent of whether tumor cells were evaluated 24 or 48 h after curcumin exposure, independent on drug concentration (Figure 2). Additional light exposure caused BrdU incorporation to become significantly reduced in all three cell lines, with effects already apparent at 0.1 μg/ml (Figure 2). Light alone did not modify BrdU uptake (data not shown).

3.2. Effect of Curcumin on Tumor Cell Apoptosis

Curcumin alone did not trigger apoptotic events in RT112, UMUC3, or TCCSUP cells. Following light exposure 0.4 μg/ml curcumin significantly enhanced the number of early apoptotic RT112 cells, and both early and late apoptotic UMUC3 cells became elevated, with strongest effects evoked at 0.4 μg/ml (Figure 3). A prominent shift towards late apoptosis was observed in TCCSUP cell cultures, particularly with 0.4 μg/ml curcumin.

3.3. Curcumin Alters Cell Cycle Progression

Cell cycling of RT112 and UMUC3 cells was not modified when curcumin was added to the cultures without light exposure (Figure 4). The amount of TCCSUP in the G2/M- and G0/G1-phase was upregulated and the number of S-phase cells was downregulated by curcumin when applied at 0.1 and 0.4 μg/ml. Light exposure enhanced the mechanistic activity of curcumin. The number of RT112 cells undergoing G0/G1 phase increased, accompanied by a decrease in the S-phase (Figure 4). The opposite was seen with respect to UMUC3, with a decrease in G0/G1 cells and an increase in G2/M- and S-phase cells. The number of TCCSUP cells in G2/M increased, whereas S-phase cells were diminished. Percentage distribution of cell cycle phases of cell cultures exposed to light, but not treated with curcumin, was similar to the controls (data not shown).

3.4. Modification of Cell Cycle Regulating Proteins

Curcumin did not influence cell cycle protein expression with a few exceptions. The amount of p27 was reduced in RT112 cells at 0.1 and 0.4 μg/ml (0.4 μg/ml > 0.1 μg/ml) curcumin, acetylated H3 and H4 increased in UMUC3 in the presence of 0.4 μg/ml curcumin and the same concentration led to an increase of p19 in TCCSUP (Figure 5). Strong effects were evoked by curcumin after light exposure. Both Cdk1 and 2 (total and phosphorylated), cyclins A, B, and D1 as well as p27 were diminished in RT112 cells. The cell cycle data show that UMUC3 cells behaved differently when curcumin and light were combined. Particularly at 0.1 μg/ml, pCdk1, Cdk2, pCdk2, and cyclin B were elevated, compared to the controls. aH3 was moderately, aH4 was massively upregulated at this concentration. Both histones, however, were not apparent in cells treated with 0.4 μg/ml curcumin. The proteins p19 and p27 were not detectable. Similar to UMUC3, the amount of Cdk-cyclin proteins increased following curcumin treatment and light exposure (0.1 > 0.4 μg/ml). This also became evident with p19 and p27. aH3 and aH4 were not detectable.

4. Discussion

Investigations have shown that curcumin potently blocks metastatic tumor progression in vitro [2123], though chemical instability and poor bioavailability hamper its clinical application. To overcome this limitation, combining curcumin with light has been found to enhance the antitumor activity. Pilot experiments with curcumin alone (without light exposure) revealed that much higher concentrations >5μg/ml were necessary to similarly suppress tumor cell growth as with low-dosed curcumin plus light. This accords with other reports where 5-50 μM curcumin was found necessary to evoke a pharmacological effect [2426]. The present investigation demonstrates that light exposure combined with low-dosed curcumin (0.1 μg/ml, 0.27 μmol/L) significantly reduces bladder cancer growth and proliferation.

The combination of light with curcumin does not amplify the antigrowth potential of curcumin in bladder cancer cells. Potent antiproliferative effects have also been observed in human keratinocytes with a curcumin concentration of only 0.2 μg/ml, when applied in combination with UVA or visible light [27]. Experimental work on melanoma and oral squamous cell carcinoma cell models have confirmed these findings [18, 28], as has light-induced sensitization of curcumin in a xenograft tumor model with human epithelial carcinoma cells [17]. Thus, the effects of curcumin-light do not seem restricted to a particular type of cancer cell.

Though an inhibitory effect of curcumin-light has been seen with several different cancer types, it is of interest that the molecular mode of action, at least in the investigated bladder cancer cell lines, was different. RT112 cells were arrested in G0/G1, UMUC3 in both the S- and G2/M-phase and TCCSUP in the G2/M-phase, exclusively. These differences were paralleled by differences in cell cycle regulating protein expression. When using 0.1 μg/ml curcumin, the Cdk1-cyclin B and Cdk2-cyclin A axes became deactivated in RT122 cells but were upregulated in UMUC3 and TCCSUP cells. Therefore, the elevation of Cdk1-cyclin B/Cdk2-cyclin A caused by curcumin-light drives UMUC3 and TCCSUP cells into the G2/M and/or the S-phase, whereas downregulation of Cdk1-cyclin B/Cdk2-cyclin A caused G0/G1 phase arrest of RT112 cells. The data obtained with 0.4 μg/ml curcumin deserve particular attention, since Cdks and cyclins were (at least) partially reduced in UMUC3 and TCCSUP cells, as well. A significant increase in the number of apoptotic UMUC3 and TCCSUP cells also occurred. Considering that curcumin induced activation of apoptotic events has been associated with suppression of Cdk1, Cyclin A and B [29, 30], we assume that UMUC3 and TCCSUP cells progress from a G2/M cell cycle arrest to apoptosis by means of a cell signaling switch. The direct transition from G2/M arrest to apoptosis might be uncommon. However, other studies have demonstrated that, prior to apoptosis, tumor cells arrested by curcumin at the G2/M transition point were then released to apoptosis by increasing the curcumin dosage [31]. The present investigation shows that curcumin plus light strongly suppresses growth in all three investigated bladder cancer cells lines, although a congeneric molecular mode of action is not apparent.

How light sensitizes curcumin’s effect is not clear, and a primary molecular mechanism has not yet been identified. Barik et al. [32] have observed a high affinity of curcumin to bovine serum albumin, associated with an enhancement of fluorescence emission and a blue-shifting of the fluorescence spectrum. Speculatively, a light dependent energy transfer during curcumin-protein-interaction may enhance the influence of curcumin on protein function and cell regulation [33].

Evidence provided that curcumin in combination with irradiation enhances its antitumor potential on bladder cancer cells. Other antitumor activity such as DNA fragmentation, release of cytochrome c from mitochondria and activation of caspases-9 and -8 caused by the combination of low curcumin concentrations and light have sufficiently been documented for other cancer types [18, 27, 34]. Therefore, curcumin, combined with visible light, seems a reasonable candidate to replace or complement BCG instillation therapy for patients with NMIBC. Indeed, photodynamic therapy through intravesically applied antitumor compounds has already been recommended as a highly effective concept to treat BCG refractory urothelial carcinomas [35, 36]. From a technical viewpoint, Bader et al. presented evidence that transmission of 2 to 6 W white light (100 J/cm2) through a single 1.5mm diameter quartz fiber assembled into a 20 Ch transurethral irrigation catheter might provide optimum activation conditions [37]. Besides treatment of NMIBC, patients not eligible for cystectomy with muscle-invasive bladder cancer (MIBC) may also profit from curcumin and subsequent light activation as an alternative to the trimodal chemotherapeutic treatment regimen formulated by Williams and colleagues [38].

Further studies are now warranted to investigate the effects of curcumin on NMIBC and MIBC in vivo.

Abbreviations

TCC:Transitional cell carcinoma
CAM:Complementary and alternative medicine
NMIBC:Nonmuscle-invasive bladder cancer.

Data Availability

The data used to support the findings of this study are included within the article.

Disclosure

Current Address of Eva Juengel is Department of Urology and Pediatric Urology, University Medical Center Mainz, Mainz, Germany.

Conflicts of Interest

We wish to confirm that there are no known conflicts of interest associated with this publication and there has been no significant financial support for this work that could have influenced its outcome.

Authors’ Contributions

Eva Juengel and Roman A. Blaheta contributed equally.

Acknowledgments

This work was supported by the Brigitta & Norbert Muth Stiftung, Wiesbaden, Germany.

References

  1. M. Burger, J. W. F. Catto, G. Dalbagni et al., “Epidemiology and risk factors of urothelial bladder cancer,” European Urology, vol. 63, no. 2, pp. 234–241, 2013. View at: Publisher Site | Google Scholar
  2. J. A. Witjes, E. Compérat, N. C. Cowan et al., “EAU guidelines on muscle-invasive and metastatic bladder cancer: summary of the 2013 guidelines,” European Urology, vol. 65, no. 4, pp. 778–792, 2014. View at: Publisher Site | Google Scholar
  3. A. Böhle, A. Jurczok, P. Ardelt et al., “Inhibition of bladder carcinoma cell adhesion by oligopeptide combinations in vitro and in vivo,” The Journal of Urology, vol. 167, no. 1, pp. 357–363, 2002. View at: Publisher Site | Google Scholar
  4. N. Perlis, A. R. Zlotta, J. Beyene, A. Finelli, N. E. Fleshner, and G. S. Kulkarni, “Immediate post-transurethral resection of bladder tumor intravesical chemotherapy prevents non-muscle-invasive bladder cancer recurrences: an updated meta-analysis on 2548 patients and quality-of-evidence review,” European Urology, vol. 64, no. 3, pp. 421–430, 2013. View at: Publisher Site | Google Scholar
  5. R. J. Sylvester, W. Oosterlinck, S. Holmang et al., “Systematic review and individual patient data meta-analysis of randomized trials comparing a single immediate instillation of chemotherapy after transurethral resection with transurethral resection alone in patients with stage pta-pt1 urothelial carcinoma of the bladder: which patients benefit from the instillation?” European Urology, vol. 69, no. 2, pp. 231–244, 2016. View at: Publisher Site | Google Scholar
  6. M. Hierl, J. Pfirstinger, R. Andreesen et al., “Complementary and alternative medicine: a clinical study in 1,016 hematology/oncology patients,” Oncology, vol. 93, no. 3, pp. 157–163, 2017. View at: Google Scholar
  7. C. Schieman, L. R. Rudmik, E. Dixon, F. Sutherland, and O. F. Bathe, “Complementary and alternative medicine use among general surgery, hepatobiliary surgery and surgical oncology patients,” Canadian Journal of Surgery, vol. 52, no. 5, pp. 422–426, 2009. View at: Google Scholar
  8. M. C. Miller, E. A. Pribitkin, T. Difabio, and W. M. Keane, “Prevalence of complementary and alternative medicine use among a population of head and neck cancer patients: A survey-based study,” Ear, Nose & Throat Journal, vol. 89, pp. E23–E27, 2010. View at: Google Scholar
  9. C. Loquai, D. Dechent, M. Garzarolli et al., “Use of complementary and alternative medicine: A multicenter cross-sectional study in 1089 melanoma patients,” European Journal of Cancer, vol. 71, pp. 70–79, 2017. View at: Publisher Site | Google Scholar
  10. M. Wojcik, M. Krawczyk, P. Wojcik, K. Cypryk, and L. A. Wozniak, “Molecular mechanisms underlying curcumin-mediated therapeutic effects in type 2 diabetes and cancer,” Oxidative Medicine and Cellular Longevity, vol. 2018, Article ID 9698258, 2018. View at: Google Scholar
  11. U. Banik, S. Parasuraman, A. K. Adhikary, and N. H. Othman, “Curcumin: the spicy modulator of breast carcinogenesis,” Journal of Experimental & Clinical Cancer Research, vol. 36, no. 1, 2017. View at: Publisher Site | Google Scholar
  12. P. S. de Campos, B. F. Matte, L. F. Diel et al., “Low doses of curcuma longa modulates cell migration and cell–cell adhesion,” Phytotherapy Research, vol. 31, no. 9, pp. 1433–1440, 2017. View at: Publisher Site | Google Scholar
  13. D. Pastorelli, A. S. C. Fabricio, P. Giovanis et al., “Phytosome complex of curcumin as complementary therapy of advanced pancreatic cancer improves safety and efficacy of gemcitabine: Results of a prospective phase II trial,” Pharmacological Research, vol. 132, pp. 72–79, 2018. View at: Publisher Site | Google Scholar
  14. H. Mahammedi, E. Planchat, M. Pouget et al., “The new combination docetaxel, prednisone and curcumin in patients with castration-resistant prostate cancer: a pilot phase ii study,” Oncology, vol. 90, no. 2, pp. 69–78, 2016. View at: Google Scholar
  15. Y. Panahi, A. Saadat, F. Beiraghdar, and A. Sahebkar, “Adjuvant therapy with bioavailability-boosted curcuminoids suppresses systemic inflammation and improves quality of life in patients with solid tumors: A randomized double-blind placebo-controlled trial,” Phytotherapy Research, vol. 28, no. 10, pp. 1461–1467, 2014. View at: Publisher Site | Google Scholar
  16. M. Kanai, Y. Otsuka, K. Otsuka et al., “A phase I study investigating the safety and pharmacokinetics of highly bioavailable curcumin (Theracurmin) in cancer patients,” Cancer Chemotherapy and Pharmacology, vol. 71, pp. 1521–1530, 2013. View at: Publisher Site | Google Scholar
  17. K. Beyer, F. Nikfarjam, M. Butting et al., “Photodynamic treatment of oral squamous cell carcinoma cells with low curcumin concentrations,” Journal of Cancer, vol. 8, no. 7, pp. 1271–1283, 2017. View at: Publisher Site | Google Scholar
  18. J. Dujic, S. Kippenberger, A. Ramirez-Bosca et al., “Curcumin in combination with visible light inhibits tumor growth in a xenograft tumor model,” International Journal of Cancer, vol. 124, no. 6, pp. 1422–1428, 2009. View at: Publisher Site | Google Scholar
  19. M. Carrion-Gutierrez, A. Ramirez-Bosca, V. Navarro-Lopez et al., “Effects of curcuma extract and visible light on adults with plaque psoriasis,” European Journal of Dermatology, vol. 25, no. 3, pp. 240–246, 2015. View at: Publisher Site | Google Scholar
  20. E. Juengel, R. Najafi, J. Rutz et al., “HDAC inhibition as a treatment concept to combat temsirolimusresistant bladder cancer cells,” Oncotarget , vol. 8, no. 66, pp. 110016–110028, 2017. View at: Google Scholar
  21. B. Tian, Y. Zhao, T. Liang et al., “Curcumin inhibits urothelial tumor development by suppressing IGF2 and IGF2-mediated PI3K/AKT/mTOR signaling pathway,” Journal of Drug Targeting, vol. 25, no. 7, pp. 626–636, 2017. View at: Publisher Site | Google Scholar
  22. M. Imran, A. Ullah, F. Saeed, M. Nadeem, M. U. Arshad, and H. A. R. Suleria, “Cucurmin, anticancer, & antitumor perspectives: A comprehensive review,” Critical Reviews in Food Science and Nutrition, vol. 58, pp. 1271–1293, 2018. View at: Google Scholar
  23. M. Kang, J.-N. Ho, H. R. Kook et al., “Theracurmin® efficiently inhibits the growth of human prostate and bladder cancer cells via induction of apoptotic cell death and cell cycle arrest,” Oncology Reports, vol. 35, no. 3, pp. 1463–1472, 2016. View at: Publisher Site | Google Scholar
  24. D. Wang, X. Kong, Y. Li et al., “Curcumin inhibits bladder cancer stem cells by suppressing Sonic Hedgehog pathway,” Biochemical and Biophysical Research Communications, vol. 493, no. 1, pp. 521–527, 2017. View at: Publisher Site | Google Scholar
  25. N. Afsharmoghadam, Z. Haghighatian, H. Mazdak, N. Mirkheshti, R. M. Koushki, and S. A. Alavi, “Concentration- dependent effects of Curcumin on 5-fluorouracil efficacy in bladder cancer cells,” Asian Pacific Journal of Cancer Prevention, vol. 18, no. 12, pp. 3225–3230, 2017. View at: Google Scholar
  26. J. Shi, X. Zhang, T. Shi, and H. Li, “Antitumor effects of curcumin in human bladder cancer in vitro,” Oncology Letters, vol. 14, no. 1, pp. 1157–1161, 2017. View at: Publisher Site | Google Scholar
  27. J. Dujic, S. Kippenberger, S. Hoffmann et al., “Low concentrations of curcumin induce growth arrest and apoptosis in skin keratinocytes only in combination with UVA or visible light,” Journal of Investigative Dermatology, vol. 127, no. 8, pp. 1992–2000, 2007. View at: Publisher Site | Google Scholar
  28. S. Buss, J. Dobra, K. Goerg et al., “Visible light is a better co-inducer of apoptosis for curcumin-treated human melanoma cells than UVA,” PLoS ONE, vol. 8, Article ID e79748, 2013. View at: Google Scholar
  29. C. Cheng, J.-T. Jiao, Y. Qian et al., “Curcumin induces G2/M arrest and triggers apoptosis via FoxO1 signaling in U87 human glioma cells,” Molecular Medicine Reports, vol. 13, no. 5, pp. 3763–3770, 2016. View at: Publisher Site | Google Scholar
  30. C. L. Kuo, S. Y. Wu, S. W. Ip et al., “Apoptotic death in curcumin-treated NPC-TW 076 human nasopharyngeal carcinoma cells is mediated through the ROS, mitochondrial depolarization and caspase-3-dependent signaling responses,” International Journal of Oncology, vol. 39, pp. 319–328, 2011. View at: Google Scholar
  31. D. K. Walters, R. Muff, B. Langsam, W. Born, and B. Fuchs, “Cytotoxic effects of curcumin on osteosarcoma cell lines,” Investigational New Drugs, vol. 26, no. 4, pp. 289–297, 2008. View at: Publisher Site | Google Scholar
  32. A. Barik, K. I. Priyadarsini, and H. Mohan, “Photophysical studies on binding of curcumin to bovine serum albumin,” Photochemistry and Photobiology, vol. 77, no. 6, pp. 597–603, 2003. View at: Publisher Site | Google Scholar
  33. A. Bernd, “Visible light and/or UVA offer a strong amplification of the anti-tumor effect of curcumin,” Phytochemistry Reviews, vol. 13, no. 1, pp. 183–189, 2014. View at: Publisher Site | Google Scholar
  34. H. K. Koon, A. W. N. Leung, K. K. M. Yue, and N. K. Mak, “Photodynamic effect of curcumin on NPC/CNE2 cells,” Journal of Environmental Pathology, Toxicology and Oncology, vol. 25, no. 1-2, pp. 205–215, 2006. View at: Publisher Site | Google Scholar
  35. A. Karl, T. Grimm, F. Jokisch, N. T. Gaisa, and C. G. Stief, “Non-muscle invasive bladder cancer : Current aspects of diagnostics, local therapy options and the update of the 2016 WHO classification,” Urologe A, vol. 55, no. 9, pp. 1247–1258, 2016. View at: Publisher Site | Google Scholar
  36. E. V. Filonenko, A. D. Kaprin, B. Y. A. Alekseev et al., “5-Aminolevulinic acid in intraoperative photodynamic therapy of bladder cancer (results of multicenter trial),” Photodiagnosis and Photodynamic Therapy, vol. 16, pp. 106–109, 2016. View at: Publisher Site | Google Scholar
  37. M. J. Bader, H. Stepp, W. Beyer et al., “Photodynamic therapy of bladder cancer - a phase i study using hexaminolevulinate (HAL),” Urologic Oncology: Seminars and Original Investigations, vol. 31, no. 7, pp. 1178–1183, 2013. View at: Publisher Site | Google Scholar
  38. S. B. Williams, Y. Shan, U. Jazzar et al., “Comparing survival outcomes and costs associated with radical cystectomy and trimodal therapy for older adults with muscle-invasive bladder cancer,” JAMA Surgery, vol. 153, no. 10, pp. 881–889, 2018. View at: Publisher Site | Google Scholar

Copyright © 2019 Frederik Roos et al. 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.


More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder
Views1258
Downloads363
Citations

Related articles

We are committed to sharing findings related to COVID-19 as quickly as possible. We will be providing unlimited waivers of publication charges for accepted research articles as well as case reports and case series related to COVID-19. Review articles are excluded from this waiver policy. Sign up here as a reviewer to help fast-track new submissions.