Morusin induces apoptosis by regulating expression of Bax and Survivin in human breast cancer cells
- Authors:
- Published online on: April 7, 2017 https://doi.org/10.3892/ol.2017.6006
- Pages: 4558-4562
Abstract
Introduction
Morusin which has been isolated from the root bark of Morus alba L. (Moraceae), known and read as SangBekPi in Republic of Korea, possesses various biological activities including antimicrobial, scavenging against superoxide anion radical and anti-inflammatory activities (1–3). Previous studies have indicated that morusin suppresses cancer cell growth, and induces cell death in cervical cancer, hepatoma, glioma and prostate cancer (4–9). The anticancer activity of morusin is mediated by inhibiting signal transducer and activator of transcription 3 (STAT3) and/or nuclear factor (NF)-κB pathways, which results in apoptosis (5–7).
Breast cancer is the most common type of cancer, and the third leading cause of cancer-associated mortality, in females worldwide with >522,000 mortalities in 2012 (15% of female mortalities) (10,11). Mortality rates for breast cancer are lowest in Eastern Asia; however, the incidence of female breast cancer has been continuously increasing in the Republic of Korea (12). Although different types of treatment including surgery, radiotherapy, chemotherapy, targeted therapy and hormonal therapy are available for patients with primary breast cancer, there are still numerous limitations in breast cancer treatment due to the complex disease factors (13). Therefore, advances in scientific knowledge and the underlying molecular mechanisms associated with breast cancer may help to reduce the incidence rate of breast cancer.
Malignant tumors usually possess the capability to avoid apoptosis and other death signals, which leads to therapeutic resistance (14,15). The modulation of apoptosis-associated proteins including Bcl-2-associated-x protein (Bax) and Survivin in tumors is the most common strategy of evading apoptosis. The pro-apoptotic protein Bax is classified as a multi-domain protein of the B-cell lymphoma 2 (Bcl-2) family that regulates mitochondrial signaling by mitochondrial outer membrane permeabilization (MOMP). Bax requires the heterodimer with Bcl-2 antagonist/killer 1 (Bak) in order to be responsible for mitochondrial dysfunction and MOMP (16). Inactivating mutations of Bax occur in numerous types of human cancer, including breast cancer, leading to the uncontrolled growth of tumors (17–19). As an anti-apoptotic protein, Survivin regulates apoptosis and the cell cycle. Survivin has been demonstrated to increase the drug resistance in cancers via caspase-dependent mechanisms. However, the inhibition of Survivin in tumor cells induces apoptotic cell death (20–23). The expression of Survivin is also modulated in the majority of human cancer types including breast cancer (20). Thus, induction of apoptosis through targeting anti- and/or pro-apoptotic proteins has recently been regarded as a potentially effective strategy for cancer treatment. In the present study, the anti-cancer activity of morusin was investigated in multiple human breast cancer cell lines.
Materials and methods
Cell culture and reagents
Human breast cancer MCF-7, MDA-MB-231, MDA-MB-157 and MDA-MB-453 cell lines and a human normal mammary epithelial MCF10A cell line were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). MDA-MB-231 cells were cultured in Dulbecco's modified Eagle's medium and the other breast cancer cell lines were cultured in RPMI-1640 supplemented with 10% fetal bovine serum (HyClone; GE HealthCare Life Sciences, Logan, UT, USA) and 1% antibiotic-antimycotic solution containing penicillin G (10,000 U/ml), streptomycin sulfate (10 mg/ml) and amphotericin B (25 µg/ml; cat. no. 30-004-CI; Mediatech; Corning, Tewksbury, MA, USA). MCF10A cells were cultured in Mammary Epithelial Basal medium with the supplements provided in the MEGM™ BulletKit™ (Lonza, Basel, Switzerland) according to the ATTC culture method (24). All cells were cultured in a humidified incubator with 5% CO2 at 37°C and the viability of cultured cells was monitored using a LUNA-FL Automated cell counter (Logos Biosystems, Inc., Anyang, Republic of Korea). Morusin was purchased from Biopurify Phytochemicals Ltd. (Chengdu, China) and dissolved in dimethylsulfoxide. MTT was purchased from Sigma-Aldrich (Merck KGaA, Darmstadt, Germany).
Cell viability assays
Cells (3–5×103 cells/well) were seeded into 96-well plates 1 day prior to treatment. Following treatment for the indicated time periods (24, 28 and 72 h) with 5–30 µM morusin, cell viability was evaluated using MTT assays as previously described (25). Cell viability values are presented as a percentage as compared with the mock-treated control.
Western blot analysis
Whole cell lysates were prepared using cell lysis buffer (cat. no. 9803) from Cell Signaling Technology, Inc. (Danvers, MA, USA), and western blotting was performed as previously described (25). Subsequent to performing the SDS-PAGE and transfer, the membranes were incubated in 5% skim milk in PBST (PBS with 0.1% Tween-20 (Sigma-Aldrich; Merck KGaA) at room temperature for 1 h for blocking, and then incubated with each primary antibody in 5% skim milk or 5% bovine serum albumin in PBST with gentle agitation overnight at 4°C. Incubations with the secondary antibodies were performed in 5% skim milk in PBST at room temperature for 1 h. Primary antibodies directed against Bax (SC-493), Bcl-2 (SC-492), Bcl-extra large (Bcl-xL) (SC-7195), cleaved caspase-3 (cs9661s), Survivin (SC-17779), poly ADP-ribose polymerase (PARP) (cs9546) (all dilution, 1:1,000), and cleaved caspase-8 (cs9496) and 9 (SC-22182) (both dilution, 1:3,000) were purchased from Santa Cruz Biotechnology, Inc. (Dallas, TX, USA) or Cell Signaling Technology, Inc. (Danvers, MA, USA) and β-actin (A5441) (dilution, 1:10,000) from Sigma-Aldrich (Merck KGaA), and horseradish peroxidase-conjugated anti-mouse Immunoglobulin G (IgG) (cs7076) or anti-rabbit IgG (cs7074) secondary antibodies (dilution, 1:5,000) from Cell Signaling Technology, Inc. were used for immunoblotting. Subsequently, the membranes were detected using a chemiluminescence system (Daeil Lab Service Co., Ltd., Seoul, Korea). β-actin was used as an internal control.
Apoptosis analysis
Cells (1–2×103 cells/well) in 6-well plates were treated with morusin at 37°C for 2 days. Apoptosis was observed using staining with Annexin V-FITC and propidium iodide (PI; BioVision, Inc., Milpitas, CA, USA) and compared with the mock-treated control group. The cells were subsequently analyzed using a BD FACSCalibur™ flow cytometer and BD CellQuest™ (BD Biosciences, Franklin Lakes, NJ, USA) as described (25).
Statistical analysis
Statistical analysis was performed using Excel 2013 (Microsoft, Redmond, WA, USA) and SigmaPlot v.13 (Systat Software, Inc., San Jose, CA, USA). Data are presented as the mean ± standard error of the mean from ≥3 independent experiments performed in triplicate or more and analyzed for statistical significance using the unpaired Student's t-test. P<0.05 was considered to indicate a statistically significant difference.
Results
Morusin suppresses cell viability in human breast cancer cells
In order to investigate the possible therapeutic effect of morusin in breast cancer, the effects of morusin on the viability of human breast cancer cells was evaluated. Human breast cancer cell lines MCF-7, MDA-MB-157, MDA-MB-231 and MDA-MB-453, and a normal immortalized breast epithelial cell line MCF10A were treated with morusin for 24, 48 and 72 h, and cell viability was measured using MTT assays. As illustrated in Fig. 1, morusin significantly suppressed cell viability in a dose- or/and a time-dependent manner in all breast cancer cell lines treated with 20 µM morusin. However, notably morusin exhibited a lesser effect on normal mammary epithelial MCF10A cells, which was not significant until 48 h of treatment. Furthermore, IC50 values indicated that morusin is a more potent cytotoxic reagent in breast cancer cells compared with that in normal cells (Table I). These results suggested that morusin is a potentially effective therapeutic agent for breast cancer.
Morusin induces apoptosis in human breast cancer cells
To investigate whether a decrease in cell viability by morusin is due to the induction of apoptosis, the effect of morusin on apoptosis in human breast cancer MCF-7 and MDA-MB-231 cells was evaluated using Annexin V/propidium iodide (PI) double staining. As illustrated in Fig. 2, 10 µM morusin significantly increased the Annexin V-positive cell population in a dose-dependent manner in MDA-MB-231 and MCF-7 cells, which is indicative of apoptosis. Furthermore, it was consistently demonstrated that morusin increased the expression of apoptotic marker proteins, cleaved caspase 9, cleaved caspase 3 and PARP cleavage, in a dose- (Fig. 3A) and time- (Fig. 3B) dependent manner. Together these results indicate that morusin induces apoptosis in human breast cancer cells.
Morusin decreases Survivin and increases Bax in human breast cancer cells
Previous studies have reported that morusin induces apoptosis by modulating STAT3 and/or NF-κB in various types of cancer cells, which are well-known transcription factors that regulate various genes involved in cellular proliferation, survival and apoptosis (5–7). Thus, the effect of morusin on the regulation of apoptosis-associated protein expression was determined in MDA-MB-231 and MCF-7 cells. As illustrated Fig. 4, morusin induced Bax and reduced Survivin expression in a dose- (Fig. 4A) and time- (Fig. 4A) dependent manner, while no effect on the expression of Bcl-2 and Bcl-xL was observed in human breast cancer cells. These results indicate that morusin induces apoptosis by regulating the pro-apoptotic protein Bax and the anti-apoptotic protein Survivin in human breast cancer cells.
Discussion
Breast cancer is the most common type of cancer and the third leading cause of cancer-associated mortality for women worldwide with >522,000 mortalities in 2012 (11). In the Republic of Korea, the incidence of breast cancer in women has been continuously increasing (12). Various therapeutic strategies for breast cancer have been developed to date. However, the overall treatment efficiency for malignant and metastatic breast cancer remains stagnant. Recent studies have identified effective phytochemicals for the treatment of cancer, including advanced stage breast cancer (26–28). Therefore, the potential of morusin as a therapeutic agent for breast cancer was evaluated in the present study. Cytotoxicity assays were used to verify whether morusin could be a therapeutic agent for breast cancer, and revealed that morusin suppressed cell viability in human breast cancer cells with an IC50 of 18–45 µM. However, morusin exhibited little toxic effect in normal breast MCF10A cells with an IC50 of >118 µM following 24 h morusin treatment, which demonstrated similar results following treatment for 48 and 72 h. Although it was revealed that morusin induced apoptosis in breast cancer cells, the apoptotic rate was lower compared with the cytotoxicity rate for the same concentration of morusin. These results indicate that morusin may induce other types of cell death, including necrosis and autophagy in breast cancer cells.
Apoptosis is an evolutionarily conserved essential process for development and tissue homeostasis (29). However, an analysis of the evidence suggests that the upregulation of anti-apoptotic proteins in cancer is considered one of the strategies of evading apoptosis (as reviewed in 30). For this reason, scientists have developed anti-cancer drugs targeting these apoptosis-associated proteins. In the present study, it was demonstrated that morusin is a candidate for anti-cancer agent to treat breast cancer by suppression of the anti-apoptotic protein Survivin (Fig. 4). Furthermore, morusin increased pro-apoptotic protein Bax expression in breast cancer cells, indicating its ability at targeting anti- and pro-apoptotic signals that may increase anticancer activity. Previous studies have reported that morusin inhibits proliferation of cancer cell by suppressing STAT3 signal (5–7). Inhibition of STAT3 subsequently affects the expression of its downstream targets, including Bax and Survivin (31,32). In the present study, morusin was revealed to modulate the expression of Bax and Survivin in human breast cancer cells, suggesting that STAT3 may be involved in this regulation.
In conclusion, the results of the present study indicate that morusin can induce apoptosis by decreasing Survivin and increasing Bax protein expression in human breast cancer cells. These results indicate that morusin may be a potentially effective anticancer agent for the treatment of patients with breast cancer.
Acknowledgements
The present study was supported by the National Research Foundation of Korea (grant nos. 2007-0054931, NRF-2013R1A1A2007263 and NRF-2014R1A1A2057918).
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