Synergistic effect of curcumin on epigallocatechin gallate-induced anticancer action in PC3 prostate cancer cells

Abstract

Epigallocatechin gallate (EGCG) and curcumin are well known to naturally-occurring anticancer agents. The aim of this study was to verify the combined beneficial anticancer effects of curcumin and EGCG on PC3 prostate cancer cells, which are resistant to chemotherapy drugs and apoptosis inducers. EGCG showed weaker inhibitory effect on PC3 cell proliferation than two other prostate cancer cell lines, LNCaP and DU145. Co-treatment of curcumin improved antiproliferative effect of EGCG on PC3 cells. The protein expressions of p21 were significantly increased by the co-treatment of EGCG and curcumin, whereas it was not changed by the treatment with each individual compound. Moreover, treatments of EGCG and curcumin arrested both S and G2/M phases of PC3 cells. These results suggest that the enhanced inhibitory effect of EGCG on PC3 cell proliferation by curcumin was mediated by the synergic up-regulation of p21-induced growth arrest and followed cell growth arrest. [BMB Reports 2015; 48(8): 461-466]

INTRODUCTION

Prostate cancer is adenocarcinoma that develops in the prostate gland, a male reproductive organ. Rate of prostate cancer is increasing in the developing as well as developed regions of the world. Factors including age, genetic background and diet have been implicated in the development of prostate cancer (1). Many men with early prostate cancer often have no symptoms or similar symptoms of diseases such as prostatic hyperplasia, and undergo no therapy. Prostate cancer may metastasize from the prostate to other parts of the body, particularly to the bones and lymph nodes (2-4). Globally, prostate cancer-related deaths constitute the sixth leading cause of death in men (1, 5).

Various bioactive agents have been used alone or as adjuncts to conventional chemotherapy to improve efficacy and reduce drug-induced toxicity (6). For example, clinical and experimental studies have shown that ingredients in green tea and turmeric roots are beneficial for patients undergoing chemotherapy, by inhibiting proliferation and inducing apoptosis against malignancies, including those of prostate cancer (7-9).

Epigallocatechin gallate (EGCG), also known as eapigallocatechin-3-gallate, is the most abundant catechin in green tea. EGCG has been intensively studied as a chemopreventive agent for head, neck, lung and prostate cancers in vitro and in vivo (7, 8, 10, 11). In prostate cancer, EGCG has been reported to induce changes in intracellular pathways, such as down-regulation of ERK1/2- and Akt-mediated signaling, inhibition of PMA-dependent PKC activation, alteration of Bcl-2 family member ratio and up-regulation of caspases (12-16). Also, inactivation of p53 using small interfering RNA rendered prostate cancer cells resistant to EGCG-mediated apoptosis (17). Curcumin, a component of turmeric, is one of the most commonly used and well-studied phytochemicals. Curcumin has been researched for its anti-tumor effects on various cancer cells and in animal models (18-20). Curcumin inhibits various cell signaling pathways at multiple levels, such as survival, proliferation, enzymes, transcription factors and cell cycle pathways (21).

It is proposed that prevention of cancer is more feasible and holds a better promise with the use of multiple agents that can hit multiple targets in the process of carcinogenesis (22, 23). There is also currently an increasing interest in the use of a combination of two or more agents, at low doses with differing modes of action, for chemoprevention (24-27). Consistent with this view, we sought to identify whether the combined beneficial anticancer effects of EGCG and curcumin exist in PC3 prostate cancer, with cells that are resistant to many chemotherapy drugs and apoptosis inducers.

RESULTS AND DISCUSSION

Combinations of natural compounds have been used successfully in the treatment of various types of cancer to gain higher therapeutic effect with lower dosage and to reduce drug resistance and/or side effects (28). Suganuma et al. recently identified that anticancer compounds from edible plants would strengthen their anticancer effect when in combination with green tea catechins (29). In the present study, we have investigated optimal adjuvant candidate of EGCG for prostate cancer treatment and identified its action mechanism.

To compare cell proliferation inhibitory effect of EGCG on three prostate cancer cell types (LNCaP, DU145 and PC3), Ez-cytox cell viability assay was performed at various concentrations for 24 h. As shown in Fig. 1A, prostate cancer cell viability was significantly decreased in a dose-dependent manner by the treatment with EGCG. The IC₅₀ values of EGCG were 159.3, 40.6 and 189.8 μM for LNCaP, DU145 and PC3 cells, respectively. Therefore, EGCG showed weaker inhibitory effect on PC3 cell proliferation than in the other prostate cancer cell lines, LNCaP and DU145. This result is in line with earlier studies. In the literature, EGCG showed strong antiproliferative effect and increased the expression of p53 protein and its downstream targets p21 and Bax in prostate cancer LNCaP cells (28). However, prostate cancer PC3 cell treated with EGCG showed lower anti-proliferation (17).

Fig. 1. Inhibitory effects of natural and synthetic anticancer agents on prostate cancer cell proliferation. (A) Comparison in inhibitory effect of EGCG on the proliferation of 3 prostate cancer cells (LNcaP, DU145 and PC3). (B) Comparison in inhibitory effect of etoposide, cisplatin, ginsenoside Rg3 and curcumin on the proliferation of PC3 cells.

Next, we compared the anticancer effects of several synthetic and natural anticancer compounds on PC3 cells to determine optimal adjuvant candidate of EGCG for prostate cancer treatment. Two synthetic (cisplatin and etoposide) and two natural compounds (curcumin and ginsenoside Rg3) were chosen based on literature search. As shown in Fig. 1B, all of the synthetic and natural compounds showed anticancer effects on PC3 cells in a dose-dependent manner. The anticancer effects of natural reagents were stronger than synthetic reagents. In particular, the anticancer effect of curcumin on PC3 cells was stronger than other reagents containing EGCG. Therefore, curcumin was suggested to be optimal adjuvant candidate of EGCG.

To evaluate the combined beneficial effect of curcumin on EGCG-induced anticancer action, PC3 cells were treated with EGCG at concentrations of 50 and 100 μM, in the presence or absence of 50 μM curcumin. As shown in Fig. 2A, EGCG inhibited PC3 cell proliferation to 11.2 and 24.3% at 50 and 100 μM, respectively. Curcumin inhibited PC3 cell proliferation to 34.8% at 50 μM. In comparison with each treatment of EGCG (50 and 100 μM) or curcumin (50 μM), anticancer effect was markedly improved by the co-treatment of EGCG and curcumin. Also, changes in cellular morphology were observed by microscopy as shown in Fig. 2B. A small portion of shrinkage in the cell morphology was shown following curcumin treatment, and progressive condensing and breaking up (karyorrhexis) in the nucleus were shown in most cells after co-treatment of EGCG and curcumin.

Fig. 2. Combined beneficial effects of EGCG and curcumin on the proliferation of PC3 prostate cancer cells. (A) Comparison in inhibitory effects of EGCG, curcumin and co-treatment of EGCG and curcumin on the proliferation of PC3 cells. (B) Representative morphological changes in cells confirmed by phase-contrast microscopy. P ＜ 0.05 compared to the control value.

Based on the antiproliferative effect of co-treatment of EGCG and curcumin on prostate cancer PC3 cells, its action mechanism was further identified by investigating the expression of tumor survival molecule p-Akt, cell cycle-related protein p21 and p-Rb and apoptotic protein caspase 3, using Western blot. As shown in Fig. 3, the expression of tumor survival molecule p-Akt was not changed by the treatments of EGCG, curcumin and co-treatment of EGCG and curcumin. However, the expression level of p21 protein was activated by the treatment of curcumin and more significantly by the co-treatment of EGCG and curcumin. The expression levels of p-Rb were slightly decreased by the treatment of EGCG and more strongly by curcumin and co-treatment of EGCG and curcumin. On the other hand, the expression of cleaved caspase 3 was not changed by the treatments of EGCG, curcumin and co-treatment of EGCG and curcumin. Therefore, induction of p21 and inhibition of p-Rb may be the main mechanisms related to the inhibition of PC3 cell proliferation.

Fig. 3. Combined beneficial effects of EGCG and curcumin on the protein expressions related to apoptosis, cell cycle and tumor suppresser genes in PC3 cells. The band intensities from each blot were quantified using Image J software and normalized to GAPDH.

Cell cycle is one of several anti-cancer targets. Down-regulation of cell cycle on uncontrolled cell proliferation and tumorigenesis can be targeted to suppress cancer progression (30). Either EGCG or curcumin is a strong inhibitor of cell cycle kinases and cell cycle related proteins (31, 32). However, the differences in actions of EGCG and curcumin on specific phases of cell cycle are not well known. Co-treatment of the two natural compounds may simultaneously affect multiple cell cycle-related target pathways. To determine whether co-treatment of EGCG and curcumin induced cancer cell cycle arrest, flow cytometry analysis was performed to measure the distribution of cell cycles using PI staining. Flow cytometry reveals distribution of cells in three major phases of the cycle (G1 vs. S vs. G2/M) and makes it possible to detect apoptotic cells. As shown in Fig. 4A, EGCG (100 μM) mainly arrested S phase of PC3 cells over control cells. However, curcumin (50 μM) arrested G2/M phase of PC3 cells over control cells. Arrests in both S and G2/M phases of cell cycle were observed by the co-treatment of EGCG and curcumin (Fig. 4B). Therefore, the combined beneficial effect of curcumin on EGCG-induced anticancer effect in PC3 cells was mediated by the induction of their different actions on cell cycle arrest.

Fig. 4. Combined beneficial effects of EGCG and curcumin on the cell cycle of PC3 cells. (A) Comparison in effects of EGCG, curcumin and co-treatment of EGCG and curcumin on PC3 cell cycle. (B) Quantitative graph for FACS analysis results. P ＜ 0.05 compared to the control value.

While curcumin has versatile anticancer properties, its poor absorption and low bioavailability are the challenges for its developmentas chemopreventive agent (33). The low bioavailability of EGCG is also confirmed in other literature (34). However, it was reported that (-)-epicatechin, another kind of green tea polyphenol, significantly increased the amounts of intracellular curcumin concentration (35), where the exact mechanism is not as yet understood. Further studies on the chemical derivatization or optimal production methods are neededfor clinical application.

In summary, antiproliferative effect of EGCG on PC3 cells was weaker than that on LNCaP and DU145 cells. However, antiproliferative effect of EGCG in PC3 cells was significantly improved after co-treatment of curcumin. The expression levels of p-Rb and p21 were decreased and increased, respectively, after co-treatment of EGCG and curcumin. EGCG and curcumin mainly arrested S and G2/M phases of PC3 cells over control cells, respectively, when treated separately. Co-treatment of EGCG and curcumin arrested both S and G2/M phases of cell cycle. These results suggest that the enhanced inhibitory effect of EGCG on PC3 cell proliferation by curcumin was mediated by the synergic up-regulation of p21 and followed cell growth arrest.

MATERIALS AND METHODS

Chemicals and reagents

EGCG was purchased from Tocris Bioscience (Bristol, UK). Etoposide, cisplatin, ginsenoside Rg3, curcumin and polyphenon 60 green tea extract were purchased from Sigma Chemical Co. (Missouri, USA). A stock solution of chemicals were prepared in 100% dimethylsulfoxide (DMSO), and stored at -20℃ until use. When required, the stock solution was diluted with cell culture media to the appropriate concentration. The final concentrations of DMSO were adjusted to less than 0.5% (v/v) in the culture media.

Cell culture

The human prostate cancer cells LNCaP, DU145 and PC3 were purchased from the American Type Culture Collection (ATCC, Rockville, USA). LNCaP and PC3 cell were maintained in RPMI-1640 (Gibco, Gaithersburg, USA) medium supplemented with 10% fetal bovine serum (Gibco, Gaithersburg, USA), 100 units/ml penicillin and 100 μg/ml streptomycin and DU145 was grown in Minium Essential Medium (MEM) (Gibco, Gaithersburg, USA) supplemented with 10% fetal bovine serum, 100 units/ml penicillin and 100 μg/ml streptomycin, and incubated at 37℃ in a humidified incubator with 5% CO₂.

Analysis of cell viability

Ez-cytox Cell viability assay kit (DOGEN, Seuol, Korea) was used to determine cell viability. Exponentially growing cells were seeded in a 96-well plate at a density of 1 × 10⁴ cells/well in triplicate. The next day, the cells were treated with various samples at various concentrations. After incubation for 24 h, media were changed to avoid interference by the colored compounds. Subsequently, 10 μl of the kit reagent was added and the cells were incubated for an additional 1 h. Then, the cell culture supernatant was collected and cell viability was measured by scanning the absorbance of supernatant with a microplate reader at 450 nm. Control cells were exposed to culture media containing 0.5% (v/v) DMSO.

Preparation of whole-cell extracts

Human prostate cancer cells were grown in 60 mm dishes and treated with various concentration of EGCG, curcumin and mixture of 100 μM EGCG and 50 μM curcumin or were not treated for 24 h. Whole cell extracts were prepared according to the manufacturer’s instructions using RIPA buffer (Cell Signaling, Beverly, USA) supplemented with 1x protease inhibitor cocktail and 1 mM phenylmethylsulfonyl fluoride (PMSF).

Western blot analysis

Proteins (whole cell extracts: 30 μg/lane) were separated by electrophoresis through a NuPAGE 4-12% Bis-tris gel (Invitrogen, Carlsbad, USA), blotted onto a PVDF transfer membrane, and analyzed with the epitope-specific primary and secondary antibodies. The bound antibodies were visualized using ECL Advance Western Blotting Detection Reagents (GE Healthcare, Waukesha, USA) and LAS-4000 (Fujifilm, Tokyo, Japan). Monoclonal antibodies to p-Akt (Ser 473), p21, GAPDH and ployclonal antibodies to PTEN, Akt, p53, Bcl-2 and p-Rb were purchased from Cell Signaling Technology, Inc. (Beverly, USA). The band intensities from each blot were quantified using Image J software and normalized to GAPDH.

Flow cytometric analysis

Cell cycle arrest was assessed by PI staining using an Annexin-V-FLUOS staining Kit (Roche, Indianapolis, USA) according to the manufacturer’s recommendations. Briefly, whole cells were collected, rinsed with DPBS, incubated with 300 μl of DPBS involved 10 μg/ml RNase A for 15 min and 12 μl of PI at RT for 15 min in the dark, and analyzed by a FACSCalibur flow cytometer. At least 20000 events were evaluated in these experiments.

Statistical analysis

Statistical significance was determined through one-way analysis of variance (ANOVA) followed by a multiple comparison test with a Bonferroni adjustment. P values of less than 0.05 were considered statistically significant.