Ethanol extract from Cnidium monnieri (L.) Cusson induces cell cycle arrest and apoptosis via regulation of the p53‑independent pathway in HepG2 and Hep3B hepatocellular carcinoma cells

Introduction

Hepatocellular carcinoma (HCC) is the most common cancer worldwide, and it is a major cause of cancer-associated mortality (1,2). HCC occurs due to multifactorial causes such as smoking, alcohol, human hepatitis virus, fatigue and obesity (3,4). The current therapy for HCC includes surgery, chemotherapy and radiotherapy. However, the therapeutic outcomes are unsatisfactory (3). Cancer cells need an energy source such as glucose and lipids for proliferation and division, and then, they spread to another part of the body from the primary site (5). A previous study reported that bioactive compounds from natural plant extracts play a crucial role as potential therapeutic agents (6). Many plant extracts induce anticancer effects such as anti-proliferative and anti-metastatic effects and cell cycle arrest in various cancer cell lines (7–9). Moreover, the anticancer activity of natural plant extracts has been investigated in HepG2 and Hep3B hepatocellular carcinoma cells (3,10).

Protein kinase B (PKB, also known as Akt) plays a significant role in various cellular functions such as cell survival, proliferation and metabolism (11). The phosphorylation of Akt at serine 473 is known to regulate Glycogen Synthase kinase-3β (GSK-3β) inactivation through phosphorylation of GSK-3β at serine 9 (12). GSK-3β is one of the two GSK-3 isoforms, and it regulates cell growth, differentiation and cell survival (13). Inactive GSK-3β induces MDM2-mediated p53 ubiquitination and degradation (13). Tumor protein p53 (p53) induces cell cycle arrest and apoptosis through transcriptional regulation of p21Cip1/Waf1, Mouse double minute 2 homolog (MDM2) and Bcl-2-associated X protein (Bax) genes, and also regulates the activation of Bak and caspase-3 (14,15). The p21 protein, one of the cyclin-dependent kinases (CDKs), can arrest cell cycle at G1 phase through inhibition of cyclin E-CDK2 complex (16). However, previous studies have suggested that p21 can induce apoptosis and cell cycle arrest via p53-dependent and p53-independent signaling pathways (16–18).

Cnidium monnieri (L.) Cusson is a well-known Chinese medicinal herb that is commonly used for treating gynecological diseases, carbuncles, ringworm and nephritis (19–21). According to previous study, the ethanol extracts from C. monnieri contains several bioactive compounds such as osthole and xanthotoxol (22). In the present study, we investigated wether ethanol extracts from C. monnieri (CME) have an influence on cell cycle arrest and apoptosis in hepatocellular carcinoma cells. Furthermore, to determine whether CME-induced cell cycle arrest and apoptosis occurred via a p53-dependent or p53-independent mechanism, we confirmed the regulation of Akt/GSK-3β and p53 signaling pathway by CME in HepG2 (wild-type p53) and Hep3B (p53-null) hepatocellular carcinoma cells.

Materials and methods

Reagent

Cnidium monnieri (L.) Cusson were purchased from Dong Kyung PHARM Co., Ltd. (Seoul, Korea). The 100 g of CME was soaked in 800 ml of 99.9% ethanol, and then stirring for 48 h at room temperature. The extract was filtered through filter paper (qualitative filter paper no. 1; Toyo Roshi Kaisha, Ltd., Tokyo, Japan) and concentrated with a rotary evaporator to remove the ethanol. The ethanol extracts of Cnidium monnieri (L.) Cusson (CME) was dissolved in dimethyl sulfoxide (DMSO; stock solution, 10–100 mg/ml) and refrigerated at −20°C for long storage. The final concentration of CME in the culture medium was controlled at 10–100 µg/ml. LY294002 (PI3K/Akt inhibitor) was purchased from Calbiochem (EMD Millipore, Billerica, MA, USA) and Pifithrin-α (p53 inhibitor) was purchased from Sigma-Aldrich (St Louis, MO, USA).

Cell culture

The human hepatocellular carcinoma cell lines HepG2 and Hep3B were obtained from the American Type Culture Collection (ATCC, Rockville, MD, USA). The cells were grown in DMEM medium (Hyclone, Laboratories Inc., Logan, UT, USA) containing 10% fetal bovine serum and 1% antibiotics (both Hyclone Laboratories Inc.) at 37°C in a 5% CO2 atmosphere. The cells were suspended by Trypsin-EDTA (Hyclone, Laboratories Inc.) and separated at 1×106 cells/ml per 100-mm plate, every 48 h.

Determination of cell viability using MTT assay

The cells were seeded at 1×104 cells/ml in 12-well plate and incubated for 24 h. Following incubation, the cells were treated with the CME (10–100 µg/ml) for 24 or 48 h at 37°C in a 5% CO2 atmosphere. The inhibitor was pre-treated for 30 min before treating CME. The respective medium was removed, and cells were incubated with 20 µl of MTT solution (5 mg/ml) in phosphate-buffered saline (PBS) for 1 h. Converted purple formazan from MTT was solubilized in dimethyl sulfoxide (DMSO). The absorbance of the solution in each well was determined using a microplate reader (model 680, Bio-Rad Laboratories, Inc., Tokyo, Japan) at 595 nm.

Measurement of cell cycle arrest

The cells were seeded at 1×106 cells/ml in 60-mm plate and incubated for 24 h. Following incubation, the cells were treated with the CME for 24 h at 37°C in a 5% CO2 atmosphere. The inhibitor was pre-treated for 30 min before treating CME. Total cells were harvested by trypsinization, collected by centrifugation, washed with 3 ml of PBS (twice). The supernatant was removed and discarded. The pellet were resuspended in 1 ml of cold 70% ethanol and freezed at −20°C for at least 3 h. Ethanol-fixed cells were centrifuged at 800 × g for 5 min and washed with 1 ml of PBS. The supernatant was removed, and ethanol-fixed cells were resuspended 500 µl of PBS. The cells were stained with 4 µl of PI (5 mg/ml) and 10 µl of RNase (10 mg/ml) for 20 min at room temperature. Fluorescence intensity was analyzed using a Flow cytometry-FACS Canto (Becton-Dickinson Biosciences, Drive Frankline Lage, NJ, USA).

Identification of apoptosis by Hoechst 33342

The cells were seeded at 1×104 cells/ml in 12-well plate and incubated for 24 h after put microscope cover glass (Marlenfeld GmbH & Co., Lauda-Königshofen, Germany) into well. Following incubation, the cells were treated with the CME (20, 40, 60 µg/ml) for 24 h at 37°C in a 5% CO2 atmosphere. After 24 h, the cells were treated with 0.7 µM Hoechst 33342 and incubated for 30 min. Cells were fixed with 3.5% formaldehyde 500 µl for 20 min and then were gently washed thrice with 150 µl of PBS for 5 min. Placed 10 µl of the mounting solution (50% glycerol) on a slide glass and covered with a cover glass. The chromatin was observed using fluorescence microscope (magnification, ×200; Axioskop 50, Carl Zeiss, Thornwood, NY, USA).

Western blot analysis

The cells were seeded at 1×105 cells/ml in 6-well plate and incubated for 24 h. Then, the cells were treated with the concentration of CME for 24 h at 37°C in a 5% CO2 atmosphere. The inhibitor was pre-treated for 30 min before treating CME. The cells were then rinsed twice with ice-cold PBS and scraped with RIPA lysis buffer (50 mM Tris-HCl pH 8.0, 150 mM NaCl, 1% NP-40, 0.5% sodium deoxycholate, 1 mM PMSF) and subjected to western blot analysis. Protein quantification was performed by Bradford assay. 30 µg of protein was loaded per lane. The Nitrocellulose membranes (0.45 µm; cat. no. 10600003; GE Healthcare Life Science, Freiburg, Germany) were blocked with 2% bovine serum albumin (BSA, Bovogen, Melbourne, Australia) in 1X TBST (24.7 mM Tris-HCl, pH 8.0, 137 mM NaCl, 0.05% Tween-20) for 1 h 30 min and incubated overnight at 4°C with primary antibodies targeting mouse monoclonal-p-Akt (Ser473) (1:2,000; cat. no. 4051), rabbit monoclonal-Akt (1:1,000; cat. no. 4685), rabbit monoclonal-GSK-3β (1:1,000; cat. no. 9315), rabbit monoclonal-Bax (1:1,000; cat. no. 5023), rabbit monoclonal-Bak (1:1,000; cat. no. 6947), rabbit monoclonal-caspase-3 (1:1,000; cat. no. 9665), rabbit polyclonal-Bcl-2 (1:2,000; cat. no. 2876), and rabbit polyclonal-β-actin (1:2,000; cat. no. 4967); all purchased from Cell Signaling Technology, Inc. (Beverly, MA, USA) and rabbit polyclonal-p-MDM2 (Ser166) (1:3,000; cat. no. ab131355), rabbit monoclonal-MDM2 (1:3,000; cat. no. ab178938), rabbit monoclonal-p21 (1:3,000; cat. no. ab109520), mouse monoclonal-cyclin E (1:3,000; cat. no. ab3927), rabbit monoclonal-p-cdk2 (Tyr15) (1:3,000; cat. no. ab76146), and rabbit monoclonal-p-cdk2 (Thr14) (1:3,000; cat. no. ab68265); all purchased from Abcam Inc. (Cambridge, MA, USA) and rabbit polyclonal-p-GSK-3β (Ser9) (1:1,000; cat. no. sc-11757-R), and mouse monoclonal-p53 (1:1,000; cat. no. sc-126) were purchased from Santa Cruz Inc. (Santa Cruz, CA, USA). After primary antibody incubation, the membranes were washed 4 times for 5 min each with 1X TBST at room temperature. Following the addition of the secondary antibody; goat polyclonal-anti-mouse antibody conjugated with HRP (1:10,000; cat. no. PA1-30126; Thermo Scientific Rockford, IL, USA) and goat anti-rabbit antibody conjugated with HRP (1:10,000; cat. no. 166-2408; Bio-Rad Laboratories, Inc., Tokyo, Japan), the membrane were reacted for 1 h 30 min at room temperature with gentle agitation. After secondary antibody incubation, the membranes were washed 4 times for 10 min each with 1X TBST at room temperature. Proteins were detected using SuperSignal West Pico Chemiluminescent Substrate (cat. no. PI34080; Thermo Scientific Rockford, IL, USA) and visualized on CP-BU new X-ray film (Agfa HealthCare, Inc., Mortsel, Belgium).

Statistics

MTT assay were statistically analyzed using an unpaired an independent sample t-test (IBM SPSS Statistics 20.0, SPSS Inc., Chicago, IL, USA). A value of P<0.05 was considered to indicate a statistically significant difference.

Results

CME treatment suppresses cell proliferation and induces cell morphology change in HepG2 cells

To determine the anti-proliferative effect of CME, we performed MTT assay after treatment with various concentrations of CME (10–100 µg/ml) for 24 and 48 h in HepG2 cells. As shown in Fig. 1A, CME inhibited cell proliferation in a dose-dependent manner (IC50 value=88.76 µg/ml in 24 h and 30.93 µg/ml in 48 h). Also, we observed the cell morphology change after treatment with CME for 24 h. As shown in Fig. 1B, cell morphology was changed by CME in a dose-dependent manner. Cell shrinkage and loss of proliferation potential were increased when cells were treated with CME (20–100 µg/ml). Furthermore, we confirmed that the number of cells that were detached from the cell culture plate was increased. These characteristics were observed during the process of apoptosis. These results indicated that CME has anti-proliferative and cell morphology change-inducing effects in HepG2 hepatoma cells.

Figure 1. Anti-proliferation and morphological change effects of CME in HepG2 cells. (A) Cell were treated with variable concentrations of CME (10–100 µg/ml) for 24 h and 48 h. Cell viability was measured by MTT assay. The statistical analysis of the data was carried out by use of an independent sample t-test. *P<0.05, **P<0.01 and ***P<0.001 vs. con (24 h). ###P<0.001 vs. con (48 h) (each experiment, n=3). (B) The cell morphology change after treatment of CME. Origin magnification, ×200. NS, not significant; CME, Cnidium monnieri (L.) Cusson extract; con, control.

CME treatment induces apoptosis in HepG2 cells

To identify whether CME-induced effects on cell growth and morphology were caused by apoptosis, we performed Hoechst 33342 staining and western blot analysis. As a result, the apoptotic DNA fragmentation was increased by CME in a dose-dependent manner (Fig. 2A). Also, the expression levels of apoptosis-associated proteins, Bax and Bak, were increased and the levels of procaspase-3 and anti-apoptotic protein Bcl-2 were decreased by CME (Fig. 2B-D).

Figure 2. CME treatment induces apoptotic DNA fragmentation and regulating expression of mitochondria-mediated apoptotic proteins in HepG2 cells. Cells were treated to with variable concentrations of CME (20–60 µg/ml) for 24 h (A) Apoptotic bodies were measured by Hoechst 33342 staining. The chromatin was observed using fluorescence microscope (magnification ×200). (B) CME effects on pro-caspase-3, Bcl-2, Bak and Bax in HepG2 cells. (C and D) Relative band intensity of mitochondria-mediated apoptotic proteins. The statistical analysis of the data was carried out by use of an independent sample t-test. *P<0.001 vs. con (each experiment, n=3). CME, Cnidium monnieri (L.) Cusson extract; Bcl-2, B-cell lymphoma 2; Bak, Bcl-2-homologous antagonist killer; Bax; Bcl-2-associated X protein con, control.

CME treatment induces cell cycle arrest at G1 phase

To confirm whether the reduced cell viability was due to cell cycle arrest, we analyzed the cell cycle after treatment with various concentrations of CME (20–60 µg/ml) for 6 h. As indicated in Fig. 3, the percentage of G1 phase in HepG2 cells was increased to 54.87% (control group), 57.94% (20 µg/ml), 61.17% (40 µg/ml) and 65.41% (60 µg/ml).

Figure 3. CME treatment induces cell cycle arrest at G1 phase in HepG2 cells. (A) Cells were treated 20–60 µg/ml of CME for 6 h. CME occurs cell cycle arrest at G1 phase. Cell cycle arrest effect was measured by flow cytometric. (B) The graph of cells ratio at each phases. CME, Cnidium monnieri (L.) Cusson extract.

CME treatment regulates the expression levels of cell cycle-related proteins in HepG2 cells

We examined the effect of CME on the expression levels of cell cycle-related proteins by CME using western blot analysis. The results showed that the expression levels of p-Akt, p-GSK-3β, p-MDM2 and cyclin E were decreased, while the levels of p53, p21, p-CDK2 (T14) and p-CDK2 (Y15) were increased in a dose-dependent manner (Fig. 4).

Figure 4. CME treatment regulates the expression levels of cell cycle-mediated proteins in HepG2 cells. (A) CME effects on p-Akt, p-GSK-3β, p-MDM2, p53, p21, p-CDK2 (Thr14), p-CDK2 (Tyr15) and cyclin E. Cells were treated 20–60 µg/ml of CME for 6 h. Protein levels were determined by Western blot analysis. The β-actin probe served as protein-loading control. (B and C) Relative band intensity of cell cycle-mediated proteins. The statistical analysis of the data was carried out by use of an independent sample t-test. *P<0.001 vs. con (each experiment, n=3). CME, Cnidium monnieri (L.) Cusson extract; p, phosphorylated; Akt, protein kinase B; GSK-3β, glycogen synthase kinase-3β; MDM2, Mouse double minute 2 homolog; p53, Tumor protein p53; p21, cyclin-dependent kinase inhibitor 1; CDK2, cyclin-dependent kinase 2.

CME-induced apoptosis and cell cycle arrest were occurred through regulation of Akt/GSK-3β signaling pathway in a p53-independent manner. To determine the association between CME-induced apoptosis and cell cycle arrest and the Akt/p53 signaling pathway, we used specific inhibitors such as LY294002 (PI3K/Akt inhibitor) and pifithrin-α (p53 inhibitor). We co-treated the cells with LY294002 or pifithrin-α and CME and performed the MTT assay. As shown in Fig. 5A, cell viabilities in the CME-treated group and the LY294002-treated group were decreased compared to that in the control group. Also, the cell viability in the CME/LY294002 co-treated group was decreased more than that in the CME-treated group. Furthermore, cell viabilities in the CME/pifithrin-α co-treated group and the CME-treated group did not differ. To confirm whether CME-induced anti-proliferative and apoptotic effects occur in a p53-independent manner, we performed the MTT assay, Hoechst 33342 staining and western blot analysis in Hep3B (p53-null) cells. As a result, CME suppressed Hep3B cell proliferation (Fig. 5B) (IC50 value=64.46 µg/ml in 24 h and 46.32 µg/ml in 48 h), and induced apoptotic DNA fragmentation in a dose-dependent manner (Fig. 5C). Also, the expression levels of apoptosis-associated proteins were regulated by CME in Hep3B cells (Fig. 5D). In the cell cycle analysis, treatment with CME or LY294002 induced cell cycle arrest at G1 phase and co-treatment with CME/LY294002 and CME/pifithrin-α also induced G1 arrest in HepG2 cells (Fig. 5E). Moreover, the percentage of G1 phase was increased by CME in Hep3B cells (Fig. 5F). These results supported the claim that CME induces apoptosis and G1 cell cycle arrest in a p53-independent manner.

Figure 5. CME induces apoptosis and cell cycle arrest in p53-independent manner in HepG2 and Hep3B cells. Cells were pre-treated with 20 µM LY294002 or 10 µM Pifithrin-α for 30 min and co-treated with 40 µg/ml CME for 24 h in HepG2 cells. Cells were treated with variable concentrations of CME (10–100 µg/ml) for 24 h and 48 h in Hep3B cells. (A) Cell viability was measured by MTT assay. The statistical analysis of the data was carried out by use of an independent sample t-test. **P<0.01 and ***P<0.001 vs. con. #P<0.05 and ###P<0.001 vs. 40 µg/ml CME-treated group (each experiment, n=3). (B) Measurement of cell viability in Hep3B (p53-null) cells. The statistical analysis of the data was carried out by use of an independent sample t-test. *P<0.05 and ***P<0.001 vs. con (24 h). #P<0.05, ##P<0.01 and ###P<0.001 vs. con (48 h) (each experiment, n=3). (C) Apoptotic bodies were measured by Hoechst 33342 staining. The chromatin was observed using fluorescence microscope (magnification ×200). (D) CME regulates expression of mitochondria-mediated apoptotic proteins in p53-independent manner. (E and F) Cell cycle arrest effect was measured by flow cytometric. CME induces G1 cell cycle arrest via p53-independent manner. NS, not significant; CME, Cnidium monnieri (L.) Cusson extract; Bcl-2, B-cell lymphoma 2; Bak, Bcl-2-homologous antagonist killer; Bax; Bcl-2-associated X protein; con, control.

CME treatment induces G1 arrest through regulation of Akt/GSK-3β signaling pathway and increase of p21 expression in a p53-independent manner

To investigate whether the CME-induced cell cycle arrest occurred through p53-independent pathway, we performed western blot analysis after treatment with LY294002 (PI3K/Akt inhibitor) and pifithrin-α (p53 inhibitor). As a result, the expression levels of p-Akt, p-GSK-3β, p-MDM2 and cyclin E were decreased in the CME-treated group compared to the control group and the expression levels in the CME/LY294002 co-treated group were also decreased (Fig. 6A). Especially, when we co-treated cells with CME and pifithrin-α, the expression levels of p-Akt, p-GSK-3β, p-MDM2 and cyclin E were decreased and the expression levels of p53, p21, p-CDK (T14) and p-CDK (Y15) were increased by CME although pifithrin-α-treatment was performed. Additionally, the expression levels of cell cycle-related proteins were regulated by CME in Hep3B (p53-null) cells (Fig. 6B).

Figure 6. CME induces G1 arrest through regulation of Akt/GSK-3β signaling pathway in p53-independent manner. (A) Co-treatment of LY294002 or Pifithrin-α with CME regulates cell cycle-mediated proteins in HepG2 cells. (B) Cells were treated with variable concentrations of CME (40–60 µg/ml) for 6 h in Hep3B cells. Protein levels were determined by western blot analysis. The β-actin probe served as protein-loading control. (C and D) Relative band intensity of cell cycle-mediated proteins in HepG2 (C) and Hep3B (D) cells. The statistical analysis of the data was carried out by use of an independent sample t-test. *P<0.001 vs. con (each experiment, n=3). NS, not significant; CME, Cnidium monnieri (L.) Cusson extract; p, phosphorylated; Akt, protein kinase B; GSK-3β, glycogen synthase kinase-3β; MDM2, Mouse double minute 2 homolog; p53, tumor protein p53; p21, cyclin-dependent kinase inhibitor 1; CDK2, cyclin-dependent kinase 2.

Discussion

Chinese medicinal herbs have been used for the treatment of various diseases in China and Southeast Asia (23). Also, many studies have focused on the anticancer effects of phytochemicals which is contained in natural plant (3,7–10). In the present study, we examined whether ethanol extracts from C. monnieri (CME)-induced apoptotic and cell cycle arrest effects were occurred by p53-dependent or p53-independent mechanism in HepG2 (wild-type p53) and Hep3B (p53-null) hepatocellular carcinoma cells.

Preferentially, we confirmed the anti-proliferative effect and cell morphological change induced by CME through the MTT assay and observation of cell morphology. HepG2 cell viability was decreased by CME in a dose- and time-dependent manner (Fig. 1A). Also, when we treated the cells with CME, the cell shrinkage and DNA fragmentation were increased and cell density was decreased in a dose-dependent manner (Fig. 1B). To determine whether the anti-proliferative effect and these characteristics occurred due to apoptosis and cell cycle arrest, we performed Hoechst 33342 staining and cell cycle analysis. Furthermore, we examined the expression levels of apoptosis and cell cycle arrest-associated proteins. In a previous study, the number of apoptotic bodies was increased by natural plant extracts in a dose-dependent manner (5,6,24). Our results showed that CME induces an increase in the number of apoptotic bodies in a dose-dependent manner (Fig. 2A). The Bcl-2 family, including Bcl-2, Bax and Bak, plays an essential role in mitochondria-dependent apoptosis (25). Bax and Bak activation induces caspase-3 activity through formation of mitochondrial membrane pore and apoptosome (26). In our study, we confirmed that CME treatment inhibited the expression of Bcl-2 and pro-caspase-3 and induced the expression of Bax and Bak proteins (Fig. 2B-D). Additionally, we determined the cell cycle arrest effect of CME by performing cell cycle analysis. When we treated the cells with CME (20–60 µg/ml), the number of G1 phase cells was increased in a dose-dependent manner (Fig. 3). Akt induces inhibition of GSK-3β through phosphorylation at Ser9 (27). Inhibited form of GSK-3β regulates p53 ubiquitination by controlling MDM2 phosphorylation (14,28). Activated p53 was translocated to the nucleus and then it induced transcription of p21 and Bax (15). p21 is a major inhibitor of Cdks which control cell cycle progression (29). Cell cycle at G1 phase is regulated by the cyclin E/CDK2 complex (16). Therefore, we determined the expression levels of cell cycle-related proteins by preforming western blot analysis. As shown in Fig. 4, the protein levels of p-Akt, p-GSK-3β, p-MDM2 and cyclin E were decreased and the protein levels of p53, p21, p-CDK2 (Thr14) and p-CDK2 (Tyr15) were increased by CME treatment.

To confirm whether CME induces apoptosis and cell cycle arrest via regulating Akt/p53 signaling pathway, we performed the experiments after pre-treatment with LY294002 (PI3K/Akt inhibitor) and Pifithrin-α (p53 inhibitor). When we treated the cells with LY294002, HepG2 cell viability was decreased compared to that in the control group (Fig. 4A). Also, cell viability in the CME/LY294002 co-treated group was decreased more than that in the CME-treated group and the Pifithrin-α-treated group was not significantly different compared to the control group. However, cell viability in the CME/Pifithrin-α-co-treated group was decreased similar to that in the CME-treated group. These results suggested that the CME-induced anti-proliferative effect occurred in a p53-independent manner. Therefore, to determine the role of p53 in the CME-induced anti-proliferative effect, we examined cell viability in Hep3B (p53-null) cells. The results showed that CME treatment reduces cell growth in a dose- and time-dependent manner (Fig. 5B).

Additionally, by performing Hoechst 33342 staining and western blot analysis in Hep3B cells, we determined that CME induces apoptotic DNA fragmentation and regulates the expression of apoptotic proteins (Fig. 5C-D). In the cell cycle analysis, the number of G1 phase cells in the LY294002-treated group and the CME/LY294002 co-treated group was increased in HepG2 cells. Moreover, co-treatment with CME and Pifithrin-α induced G1 cell cycle arrest (Fig. 5E). In Hep3B cells, CME also induced G1 cell cycle arrest (Fig. 5F). Our results determined that CME-induced apoptosis and G1 cell cycle arrest effects occurred in a p53-independent manner.

To investigate the CME-induced G1 cell cycle arrest which occurred via p53-independent signaling pathway, we identified the expression of cell cycle regulation proteins after treatment with CME and LY294002 or Pifithrin-α. The results showed that the expression levels of p-Akt, p-GSK-3β, p-MDM2 and cyclin E were decreased and the expression levels of p53, p21, p-CDK2 (Thr14) and p-CDK2 (Tyr15) were increased in the CME/LY294002 and the CME/Pifithrin-α co-treated groups (Fig. 6A and C). Furthermore, cell cycle-related proteins including p-Akt, p-GSK-3β, p-MDM2, p21, cyclin E, p-CDK2 (Thr14) and p-CDK2 (Tyr15) were regulated except for p53 protein (Fig. 6B and D). According to a previous study, GSK-3β phosphorylates MDM2 protein and overexpression of MDM2 promotes degradation of p21 through proteasome-mediated degradation in a p53-independent manner (30,31). Also, many of the studies have reported that natural extracts induce apoptosis and cell cycle arrest through controlling the p53-independent signaling pathway (32–34). Moreover, overexpression of p21 induces the expression of pro-apoptotic protein Bax and modulates the Bcl-2:Bax ratio in Hep3B cells (35).

In conclusion, CME treatment induces apoptosis and cell cycle arrest at G1 phase in HepG2 and Hep3B hepatocellular carcinoma cells. Also, these anticancer effects occurred through increase of p21 protein expression by Akt/GSK-3β/MDM2 signaling pathway in a p53-independent manner.

References