VSports手机版 - Potentiation of resveratrol-induced apoptosis by matrine in human hepatoma HepG2 cells

Introduction

Liver cancer is the fifth most common cancer in men and the seventh in women; it accounts for 9% of all cancer-related deaths worldwide and 12% in developing countries (1). Epidemiologic studies have shown that the main risk factors for hepatocellular carcinoma (HCC) are chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infections (2,3). Among primary live cancers, HCC accounts for almost 70–85% of the total liver cancer burden. Until recently, there is still a lack of systemic chemotherapy in treating HCC efficaciously VSports最新版本. Although sorafenib has been approved by FDA for the treatment of advanced HCC, it causes several adverse effects including diarrhea, hand-foot skin reaction, hypophosphatemia and the risk of bleeding (4,5). Therefore, it is urgent to develop alternative therapeutic strategies for liver cancer.

Resveratrol, a naturally occurring polyphenolic compound, is commonly present in the skin of grapes and in red wine (6) V体育平台登录. Due to its high toxicity toward tumor cells, resveratrol appears to be a good candidate drug for cancer therapy. Resveratrol can delay or prevent all stages of carcinogenesis in vitro and in vivo, including initiation, promotion and progression (6,7). When resveratrol is combined with other anticancer agents, such as 5-fluorouracil and curcumin, they display synergistic anticancer properties (8–10). Previous studies have also demonstrated that resveratrol inhibits cell proliferation and induces apoptotic cell death in HCC cells in vivo and in vitro (7).

Matrine is an important ingredient of a traditional Chinese herb Sophora flavescens Ait VSports注册入口. , which has widely been used in China for the treatment of viral hepatitis, liver cirrhosis, cardiac arrhythmia and skin inflammations without any obvious side-effects (11). Recently, its anticancer activity has been extensively investigated; it inhibits proliferation and metastasis and induces apoptosis in a variety of malignant cells (12–15). It also reduces the occurrence of multidrug-resistant tumor cells induced by chemotherapy and displays synergistic activities with other anticancer agents (16,17). Matrine inhibits the growth of HCC cells by inducing apoptosis via upregulation of the ratio of Bax/Bcl-2 (13). However, matrine alone weakly inhibits proliferation of cancer cell lines with an IC50 value of 2–16 mM (17).

In the present study, we first evaluated the antiproliferative effect of resveratrol on HepG2 cells and then explored the underlying molecular mechanisms. Since both resveratrol and matrine independently exert anticancer activities against liver cancer cells, it led us to hypothesize that an increased benefit would result when using the combination of these two agents when compared with each single agent alone. Thus, the anticancer effect of the combination treatment of resveratrol and matrine was also evaluated in HepG2 cells.

Materials and methods

Cell culture and reagents

Matrine (purity >98%) was obtained from the National Institute for the Control of Pharmaceutical and Biological Products (Beijing, China). Resveratrol (purity ≥99%), 3-(4,5-dimethyl-2-thiazoyl)-2,5-di-phenyl-2H-tetrazolium bromide (MTT) and propidium iodide (PI) were purchased from Sigma-Aldrich (St. Louis, MO, USA). The Annexin V/PI double staining kit was purchased from Nanjing KeyGen Biotech., Co., Ltd. (Nanjing, China). The HepG2 cells were purchased from the American Type Culture Collection (Rockville, MD, USA). The cells were maintained in DMEM supplemented with 10% fetal bovine serum, 100 μg/ml streptomycin and 100 U/ml penicillin at 37°C in a humidified atmosphere with 5% CO2.

Cell viability assay

MTT assay was used to assess cell viability. HepG2 cells were seeded into 96-well plates at a cell density of 5,000/well and allowed to adhere for 24 h, followed by resveratrol and/or matrine treatment for 48 h. Then 5 μl of 5 mg/ml MTT was added to the medium and incubated for 2 h at 37°C. After removing the culture medium, 100 μl of DMSO was added. The plates were read using an enzyme-linked immunosorbent assay plate reader at 570 nm. All experiments were performed in triplicate, and the cell viability of HepG2 cells was calculated as the ratio of each experimental condition to the control. The IC50 value was calculated from the nonlinear regression analysis.

Cell cycle analysis

To determine cell cycle distribution, HepG2 cells were treated with resveratrol for 24 h. The cells were trypsinized and fixed with cold 70% ethanol overnight at 4°C. Then the fixed cells were washed twice with phosphate-buffered saline (PBS) and incubated with 100 μg/ml of ribonuclease A at 37°C for 30 min and then stained with 50 μg/ml PI for 1 h. The fluorescence intensity was detected using BD FACSCalibur cytometer, and the cell cycle distribution was assayed using ModFit LT software (both from BD Biosciences, San Jose, CA, USA).

Colony formation assay

HepG2 cells were seeded into 6-well plates at a density of 400 cells/well. After overnight incubation, the cells were exposed to resveratrol and/or matrine for 48 h. Thereafter, the drugs were removed by replacing the medium with fresh medium, and the cells were then maintained in culture for another 10 days and the medium was replaced every three days, during which time the surviving cells produced colonies. The colonies were visualized by staining for 4 h with 1% methylene blue (in 100% methanol), and the colonies that contained >50 cells were counted. The colony formation efficacy was calculated according to the following formula: Colony formation efficacy = colony counts/seeded cells × 100%. All experiments were performed in triplicate.

Synergy between the resveratrol and matrine combination

The nature of the combined effect of resveratrol and matrine was determined using the method described by George et al (9), based on the principles described by Chou and Talalay (18). In brief, the expected value of the combined effect between agent 1 and 2 is calculated as: [(observed agent 1 value)/(control value)] × [(observed agent 2 value)/(control value)] × (control value); and the ratio is calculated as (expected value)/(observed value). A ratio of >1 indicates a synergistic effect, and a ratio of <1 indicates a less than additive effect.

Quantification of apoptosis

HepG2 cells were seeded in 6-well plates at a density of 3×105 cells/well and exposed to resveratrol and/or matrine treatment for 48 h. The cells were harvested and washed twice in PBS, and then resuspended in 500 μl binding buffer at a density of 1×106 cells/ml. The cell suspension was incubated with 5 μl Annexin V and 5 μl PI in the dark for 15 min at room temperature. Finally, apoptotic cells were detected by flow cytometry. The amount of apoptosis was evaluated as the percentage of Annexin V+/PI− and Annexin V+/PI+ cells.

Western blot analysis

Western blot analysis was performed as previously described (19). In brief, after treatment with resveratrol and/or matrine, HepG2 cells were collected, lysed and subjected to 7.5–12.5% sodium dodecyl sulfate-polyacrylamide gel and transferred onto a polyvinylidene fluoride membrane. After blocking with 5% non-fat milk in the blocking buffer (PBS containing 0.1% Tween-20, pH 7.5), the membrane was probed with designated first and second antibodies. The immunoreactive bands were visualized using the ECL Plus Western Blotting Detection System (Piscataway, NJ, USA). The level of β-actin was used as a loading control. The antibody against caspase-3 and caspase-9, poly(ADP-ribose) polymerase-1 (PARP-1), p53, survivin, Bax, Bcl-2 were purchased from Cell Signaling Technology, Inc. (Danvers, MA, USA). The antibodies against β-actin were purchased from Sigma-Aldrich.

Reactive oxygen species (ROS) and mitochondrial membrane potential (Δψm) assays

HepG2 cells were seeded into 6-well plates at a density of 3×105 cells/well. After overnight incubation, the cells were treated with resveratrol and/or matrine for 24 h. Then the HepG2 cells for the detection of ROS were incubated with 10 μM H2DCFDA at 37°C for 30 min in the dark. For the Δψm assay, the HepG2 cells were incubated with 0.5 mM Rhodamine 123 at 37°C for 30 min in the dark. The intracellular fluorescence intensity was measured with a BD FACSCalibur cytometer.

Statistical analysis

All experiments were repeated as least three times. One-way analysis of variance (ANOVA) was used to analyze the variance for the means of multiple groups. Statistical analysis was performed using SPSS, and significant differences were considered at values of P<0.05.

Results

Resveratrol inhibits HepG2 cell proliferation

The effect of resveratrol on the cell proliferation of HepG2 cells was evaluated by the MTT assay. The viability of HepG2 cells was decreased significantly when resveratrol was used at concentrations >10 μM (P<0.05) (Fig. 1). The cell viabilities at 10, 20, 50 and 100 μM concentrations of resveratrol were recorded as 91, 83, 70 and 46%, respectively. The results showed that resveratrol inhibited the growth of HepG2 cells in a dose-dependent manner. The IC50 value was 70 μM after incubation for 48 h.

Figure 1 Effect of resveratrol on the cell proliferation of HepG2 cells. HepG2 cells were treated with increasing concentrations of resveratrol (0, 5, 10, 20, 50, 100, 200 μM) for 48 h, and the percentage of viable cells was then determined using the MTT assay. Error bars represent the means ± SEM for three independent experiments.

Resveratrol arrests HepG2 cells in the G1 and S phase in HepG2 cells

To explore the growth-inhibitory mechanisms of resveratrol, the effect of resveratrol on cell cycle perturbations was examined. The cell cycle profile was assessed in HepG2 cells after exposure to 0, 20, 50 and 100 μM resveratrol for 24 h. A clear dose-dependent cell cycle arrest was observed in the HepG2 cells (Fig. 2). At lower concentrations of resveratrol (20 and 50 μM), the number of HepG2 cells increased in the S phase. However, when resveratrol was used at a higher concentration (100 μM), there was a considerable accumulation of cells in the G1 phase. These results indicate that resveratrol arrests the cell cycle in the G1 and S phase in a concentration-dependent manner.

Figure 2 Effect of resveratrol on the cell cycle distribution of HepG2 cells. HepG2 cells were subjected to cell cycle analysis after treatment with (a) 0, (b) 20, (c) 50 and (d) 100 μM resveratrol for 24 h. A representative result of three independent experiments is shown.

Resveratrol triggers apoptosis in HepG2 cells

In order to determine whether apoptosis participates in resveratrol-induced cell death, the expression levels of PARP-1, Bcl-2, Bax, p53, caspase-3 and -9 were measured by western blotting. Resveratrol increased PARP-1 cleavage and caspase-3 and caspase-9 activation, which are hallmarks of an increase in apoptosis, in a dose- and time-dependent manner (Fig. 3). Resveratrol also inhibited anti-apoptotic protein Bcl-2 expression and upregulated expression of pro-apoptotic protein Bax and tumor suppressor protein p53. Therefore, resveratrol induced apoptotic cell death via a caspase- and p53-dependent pathway.

Figure 3 Effect of resveratrol on the apoptosis of HepG2 cells. HepG2 cells were treated with various concentrations of resveratrol (0, 25, 50, 100 and 200 μM) for 48 h (A) or 100 μM resveratrol for the indicated times (B) and then western blotting was used to analyze the status of PARP-1, p53, Bax, Bcl-2, caspase-3 and -9. β-actin was used as a loading control. A representative result of three independent experiments is shown. PARP-1, poly(ADP-ribose) polymerase-1.

Resveratrol and matrine synergistically inhibit the growth of HepG2 cells

The effect of matrine on the growth of HepG2 cells was evaluated by the MTT assay. Matrine inhibited the growth of HepG2 cells in a dose-dependent manner (Fig. 4A). However, matrine treatment at concentrations <2 mM only resulted in a slight decrease in cell survival rate. To assess whether matrine can enhance the anticancer activity of resveratrol, we treated HepG2 cells with increasing concentrations of resveratrol (25, 50, 100 and 200 μM) in the presence or absence of matrine (1 or 2 mM) for 48 h. The MTT assay results showed that the combination treatment was more effective in inhibiting the proliferation of HepG2 cells when compared with either agent alone (Fig. 4B).

Figure 4 Combined effect of resveratrol and matrine on HepG2 cell proliferation. (A) HepG2 cells were treated with increasing concentrations of matrine (0, 0.5, 1.0, 2, 4, 8 and 12 mM) for 48 h, and the percentage of viable cells was then determined using the MTT assay. (B) HepG2 cells were treated with matrine (1 or 2 mM) and increasing concentrations of resveratrol (0, 25, 50, 100 and 200 μM), alone or in combination, and then the percentage of viable cells was determined by the MTT assay. (C) Colony formation assay was used to confirm the growth-inhibitory effect of resveratrol (0, 50 and 100 μM) with or without 2 mM matrine. Error bars represent the means ± SEM for three independent experiments. *P<0.05 compared with the control, #P<0.05 compared with each agent alone. MAT, matrine. RES, resveratrol.

In order to confirm the growth-inhibitory effect of the combination treatment of resveratrol and matrine, a colony formation assay was also used to further study the combined treatment of resveratrol and matrine. HepG2 cells were treated with increasing concentrations of resveratrol (50 and 100 μM) with or without 2 mM matrine. When resveratrol was combined with matrine, the colony formation efficacy of the HepG2 cells was significantly reduced when compared with either agent alone (P<0.05) (Fig. 4C). The precise nature of this combination was further analyzed by the method described by George et al (9). The expected effect of the combination treatment on the cell proliferation was greater than the observed combination, suggesting a synergistic effect between resveratrol and matrine on HepG2 cells (Table I). Based on these results, we selected 50 μM resveratrol and 100 μM resveratrol in the presence or absence of matrine (2 mM) to carry out the subsequent studies.

Table I Synergistic antiproliferative effect between resveratrol and matrine combination on HepG2 cells.

Table I

Synergistic antiproliferative effect between resveratrol and matrine combination on HepG2 cells.

Treatment	Observed value	Expected value	Ratioa
50 μM resveratrol+matrine	0.12	0.51	4.25
100 μM resveratrol+matrine	0.07	0.35	5.00

a Ratio = (expected value/observed value). A ratio of >1 indicates a synergistic effect and a ratio of<1 indicates a less than additive effect.

Matrine enhances resveratrol-induced apoptosis in HepG2 cells

To understand the molecular basis of the growth-inhibitory mechanism caused by resveratrol and matrine, Annexin V/PI double staining was used to quantify the extent of apoptosis after 48 h treatment with resveratrol and/or matrine. When matrine was combined with resveratrol, matrine significantly enhanced resveratrol-induced apoptosis of HepG2 cells (P<0.05) (Fig. 5A). We further detected the effects of resveratrol and/or matrine on apoptosis-related proteins. The combination treatment of resveratrol and matrine significantly enhanced the cleavage of PARP-1, activation of caspase-3 and caspase-9 when compared to either agent alone (Fig. 5B). In addition, the combined treatment significantly inhibited survivin expression in HepG2 cells compared to the expression following treatment with either agent alone.

Figure 5 Enhancing resveratrol-induced apoptosis by matrine in HepG2 cells. HepG2 cells were treated with (a) 0, (b) 50 μM RES, (c) 100 μM RES, (d) 2 mM MAT, (e) 2 mM MAT+50 μM RES, (f) 2 mM MAT+100 μM RES for 48 h. (A) Annexin V/PI double staining was used to quantify apoptosis. The amount of apoptosis was evaluated as the percentage of Annexin V+/PI− and Annexin V+/PI+ cells. (B) Western blotting was used to analyze the status of PARP-1, caspase- 3, -9 and survivin. β-actin was used as a loading control. *P<0.05 compared with the control, #P<0.05 compared with each agent alone. RES, resveratrol; MAT, matrine; PARP-1, poly(ADP-ribose) polymerase-1.

Combined treatment of resveratrol and matrine induces ROS generation and decreases Δψm in HepG2 cells

In order to study the mechanisms of the apoptosis induced by the combined treatment, we further examined the combined effect of resveratrol and matrine on ROS production in HepG2 cells after 24 h treatment. The combined treatment significantly induced ROS generation in the HepG2 cells when compared with either agent alone (P<0.05) (Fig. 6A). To better characterize the apoptotic cell death induced by resveratrol and matrine in HepG2, the role of mitochondria was also evaluated after the treatment of resveratrol and/or matrine for 24 h. The combined treatment of resveratrol and matrine caused a marked loss of Δψm in the HepG2 cells in respect to each agent alone (P<0.05) (Fig. 6B).

Figure 6 Induction of ROS generation and disruption of Δψm by the combined treatment of resveratrol and matrine in HepG2 cells. HepG2 cells were treated with (a) 0, (b) 50 μM RES, (c) 100 μM RES, (d) 2 mM MAT, (e) 2 mM MAT+50 μM RES, (f) 2 mM MAT+100 μM RES for 48 h. (A) After treatment, the cells were stained with H2DCFDA for 30 min and then analyzed by flow cytometry. (B) After staining with Rhodamine 123 for 30 min, the cells were assayed with a FACSCalibur. *P<0.05 compared with the control, #P<0.05 compared with each agent alone. ROS, reactive oxygen species; MAT, matrine. RES, resveratrol.

Discussion

Previous studies have demonstrated that resveratrol inhibits the proliferation of various types of tumor cells in vivo and in vitro (20–22). In the present study, we showed that resveratrol decreased the viability of HepG2 cells in a dose-dependent manner. In addition, we further dissected the mechanisms underlying the antitumor effect of resveratrol. Resveratrol arrested HepG2 cells in the G1 and S phase which is consistent with reported findings (23), suggesting that retardation of cell cycle progression may be one of the mechanisms underlying the antitumor effect of resveratrol.

Apoptosis, or programed cell death, is a well-documented phenomenon in many cellular systems, which has been recognized as a major anticancer therapeutic response (24). Our findings are consistent with previous reports that resveratrol induces apoptosis in cancer cells (25–27). In the present study, we confirmed that resveratrol induced apoptosis in HepG2 cells, as shown by the cleavage of PARP-1, the upregulation of p53 expression and the activation of caspase-9 and caspase-3. Caspase-9 is an initiator in the mitochondrial death pathway (the intrinsic pathway), which could be activated by apoptosomes formed by cytochrome c, Apaf-1 and pro-caspase-9 (28). Then activated caspase-9 can cleave and activate caspase-3. Caspase-3, as an effector caspase, initiates the hallmark of the degradation process of apoptosis, such as cell shrinkage, membrane blebbing, DNA fragmentation and finally the breakdown of the cell into smaller units (apoptotic bodies) (29). The Bcl-2 family members Bax and Bcl-2 serve as critical regulators of the mitochondrial-dependent apoptotic pathway. Bcl-2 that negatively regulates apoptosis promotes cell survival, whereas Bax that positively regulates apoptosis stimulates mitochondrial damage (30). Consistent with the ability of resveratrol to kill HepG2 cells via apoptotic processes, resveratrol upregulated the ratio of Bax/Bcl-2, indicating that the increased ratio of Bax/Bcl-2 may trigger resveratrol-induced apoptosis in HepG2 cells.

Matrine has been approved as an adjuvant drug for the treatment of various malignant cancers in China (11). However, matrine alone weakly inhibits proliferation of cancer cell lines with an IC50 value of 2–16 mM (17). Combination of anticancer agents for cancer therapy and prevention has been extensively studied in numerous in vivo and in vitro models (31,32). Since each agent may have its own targets and also share common targets, the combination of two anticancer agents may exert a synergistic effect. Thus, the effect of the combined treatment of resveratrol and matrine on HepG2 cells was also evaluated here. The combined treatment significantly enhanced the antiproliferative effect when compared with either agent alone. The ratio of expected value/observed value was >1 for the concentrations tested, indicating that the combined treatment of resveratrol and matrine exhibited a synergistic antiproliferative effect. To our knowledge, the present study was the first to investigate the effect of the combination treatment of resveratrol and matrine on cancer cells. The combination treatment significantly induced apoptotic cell death in HepG2 cells as compared to either agent alone, indicating that induction of apoptosis is an important mechanism of enhancing the anticancer effects of resveratrol by matrine.

Survivin is a member of the inhibitors of apoptosis-related proteins, which has been found to be frequently overexpressed in most types of cancer cells, including HCC cells. Therefore, survivin has emerged as a potential therapeutic target for natural anticancer compounds (33,34). Our results showed that the combination treatment of resveratrol and matrine significantly reduced the expression of survivin in HepG2 cells compared with the control or either drug alone. These data suggest that downregulation of survivin expression is also involved in the antiproliferative effects of the combined treatment.

ROS are known to disrupt Δψm, and therefore trigger a series of mitochondrial-associated events (35). A high level of ROS leads to oxidative stress, loss of cell function and ultimately apoptosis or necrosis (36). Natural products may exert anticancer effects by inducing ROS-mediated apoptosis. Both resveratrol and matrine were found to induce ROS production in cancer cell lines (37–39). However, there is no evidence of the combined effect of resveratrol and matrine on ROS generation. In the present study, we demonstrated that the combination treatment significantly enhanced the generation of ROS in HepG2 cells when compared with either agent alone. Furthermore, the combined treatment also resulted in loss of Δψm. Therefore, induction of ROS generation and disruption of Δψm are involved in potentiating resveratrol-induced apoptosis by matrine.

Taken together, resveratrol exhibits multiple anticancer effects by inducing cell growth inhibition, cell cycle arrest and apoptosis in HepG2 cells. Moreover, the present study is the first to demonstrate that the combination treatment of resveratrol and matrine exhibits a synergistic antiproliferative effect on HepG2 cells. Therefore, the combined treatment of resveratrol and matrine is an effective and promising strategy for the prevention and treatment of liver cancer.

Acknowledgements

This study was supported by the Central Research Institutes of Basic Research and Public Service Special Operations in 2013.

References