Metformin enhances tamoxifen-mediated tumor growth inhibition in ER-positive breast carcinoma
- Ji Ma†1, 2, 3,
- Yan Guo†1, 2,
- Suning Chen†4,
- Cuiping Zhong5,
- Yan Xue1,
- Yuan Zhang1,
- Xiaofeng Lai2,
- Yifang Wei2,
- Shentong Yu2,
- Jian Zhang2Email author and
- Wenchao Liu1Email author
© Ma et al.; licensee BioMed Central Ltd. 2014
Received: 31 October 2013
Accepted: 5 March 2014
Published: 11 March 2014
Tamoxifen, an endocrine therapy drug used to treat breast cancer, is designed to interrupt estrogen signaling by blocking the estrogen receptor (ER). However, many ER-positive patients are low reactive or resistant to tamoxifen. Metformin is a widely used anti-diabetic drug with noteworthy anti-cancer effects. We investigated whether metformin has the additive effects with tamoxifen in ER-positive breast cancer therapy.
The efficacy of metformin alone and in combination with tamoxifen against ER-positive breast cancer was analyzed by cell survival, DNA replication activity, plate colony formation, soft-agar, flow cytometry, immunohistochemistry, and nude mice model assays. The involved signaling pathways were detected by western blot assay.
When metformin was combined with tamoxifen, the concentration of tamoxifen required for growth inhibition was substantially reduced. Moreover, metformin enhanced tamoxifen-mediated inhibition of proliferation, DNA replication activity, colony formation, soft-agar colony formation, and induction of apoptosis in ER-positive breast cancer cells. In addition, these tamoxifen-induced effects that were enhanced by metformin may be involved in the bax/bcl-2 apoptotic pathway and the AMPK/mTOR/p70S6 growth pathway. Finally, two-drug combination therapy significantly inhibited tumor growth in vivo.
The present work shows that metformin and tamoxifen additively inhibited the growth and augmented the apoptosis of ER-positive breast cancer cells. It provides leads for future research on this drug combination for the treatment of ER-positive breast cancer.
KeywordsMetformin Tamoxifen Estrogen receptor Breast cancer
Tamoxifen, a non-steroidal anti-estrogen, is the most widely used anti-estrogen for the treatment or prevention of estrogen receptor (ER)-positive breast cancer [1, 2]. For women with ER-positive breast cancer, treatment for 5 years with adjuvant tamoxifen substantially reduces the rate of recurrence . Recent trials have shown that continuing tamoxifen for 10 years rather than stopping at 5 years produces a further reduction in recurrence and mortality . However, many ER positive patients are low reactive or resistant to tamoxifen  and such long treatment with tamoxifen causes serious side-effects such as increases in endometrial hyperplasia and carcinomas , an excess of venothrombotic episodes, and the development of de novo or acquired tamoxifen resistance [6, 7]. Thus, there is the need for a more effective therapy with fewer side-effects for these patients. Modulation of tamoxifen sensitivity that results in lessening of its side-effects is a desirable goal.
Metformin (1,1-dimethylbiguanide hydrochloride) is a biguanide commonly used to treat type 2 diabetes mellitus. It is frequently referred to as an “insulin sensitizer” because it lowers circulating insulin levels in settings of insulin resistance and hyperinsulinemia [8, 9]. Much recent interest has focused on the antitumor effects of metformin. A recent retrospective analysis examined the effects of metformin on potentiation of chemotherapy in breast cancer patients and found that women with diabetes and breast cancer receiving metformin and neoadjuvant chemotherapy experienced a higher pathologic complete response rate than diabetic patients just receiving neoadjuvant chemotherapy, but not metformin . This study generated substantial enthusiasm that metformin might enhance the efficacy of other anti-tumor agents, particularly endocrine drugs. In addition, emerging evidence suggests that metformin may activate AMPK and inhibit mTOR signaling to exert anti-tumor effects [11–13]. Of note, tamoxifen also represses mTOR signaling to restrain ER-positive breast cancer growth . In a phase II GINECO study, everolimus, an mTOR inhibitor, also enhanced the efficacy of tamoxifen in ER-positive metastatic breast cancer patients . It was postulated that the pleiotropic actions of metformin on AMPK/mTOR signaling might play an additive role with tamoxifen and allow its use in non-diabetic patients and women with ER-positive tumors.
Based on these considerations, we posed the following questions: first, whether metformin and tamoxifen have synergic effects on the growth of ER-positive breast cancer cells; second, whether AMPK/mTOR or other signaling pathways are involved in the two-agent synergic effects; and last, whether this synergic effect occurs in vivo. In this study, we tested the hypothesis that the combination of metformin and tamoxifen suppresses the growth of ER-positive breast cancer, and we provide evidence of basic research for future clinical trials.
Reagents and antibodies
Metformin (1,1-dimethylbiguanide hydrochloride), tamoxifen (4-hydroxytamoxifen), thiazolyl blue tetrazolium bromide (MTT), Giemsa stain, dimethyl sulfoxide (DMSO) and agarose were purchased from Sigma-Aldrich (St. Louis, MO, USA). Metformin was dissolved in sterile water to make a 1 M stock solution, and tamoxifen was dissolved in ethanol to make a 3.2 mM stock solution. The Cell-LightTM BrdU DNA Cell Proliferation Kit was purchased from Ribobio (Guangzhou, China). The antibodies against p-AMPK (Thr172), AMPK, p-mTOR (Ser2448), mTOR, p-p70S6 (Thr389), p70S6, bcl-2 and bax are rabbit monoclonals and were purchased from Cell Signaling Technologies (Beverly, MA, USA). The antibody against β-actin is a mouse monoclonal and was purchased from Boster (Wuhan, China).
The human breast cancer cell lines MCF-7 and ZR-75-1 were obtained from the American Type Culture Collection. The cells were cultured in DMEM supplemented with 10% fetal bovine serum (FBS) and were maintained in a humidified environment containing 5% CO2 and air at 37°C. The culture medium of MCF-7 cells contained 0.01 mg/ml insulin.
Cell survival assay
Cells were seeded in a 96-well plate (5 × 103 cells per well) and incubated for 24 h. After treatment with different drugs for 48 or 96 h, the cells were then incubated with 0.5 mg/ml MTT (Sigma). Four hours later, the medium was replaced with 150 μl dimethyl sulfoxide (DMSO) (Sigma) and vortexed for 10 min. Absorbance was then recorded at 490 nm using an Infinite® F500 micro-plate reader (TECAN). Relative values of optical density were calculated.
DNA replication activity assay
DNA replication activity was examined using BrdU (5-bromo-2-deoxyuridine). Cells grown on coverslips (Fisher) were treated with different drugs for 48 h. The cells were then incubated with BrdU for 1 h and stained with an anti-BrdU antibody (Ribobio) according to the manufacturer’s instructions. The results were analyzed using a fluorescence microscope (Olympus).
Plate colony formation assay
Cells (1 × 103) treated with different drugs were seeded into 60 mm dishes with 5 ml of DMEM. After 10 days, the resulting colonies were rinsed with PBS, fixed with methanol at -4°C for 5 min, and stained with Giemsa (Sigma) for 20 min. Counting was performed only on clearly visible colonies (diameter > 50 μm).
Cells (1 × 103) were added to 3 ml of DMEM with 0.3% agar and layered onto 6 ml of 0.5% agar beds in 60 mm dishes. Cells were treated with different drugs and cultured for 2 weeks, after which colonies were photographed. Colonies larger than 50 μm in diameter were counted as positive for growth.
Flow cytometry analysis
Cells (5 × 105) were collected and washed twice with PBS and then resuspended in 500 μl of staining solution containing fluorescein isothiocyanate (FITC)-conjugated annexin V antibody (5 μl) and propidium iodide (PI, 5 μl of 250 μg/ml stock solution). After incubation for 15 min at room temperature in the dark, cells were immediately analyzed on a flow cytometer. Apoptotic cells were double stained with annexin V and PI. The percentage of cells undergoing apoptosis was determined.
Western blot was performed as described previously . The blots were probed with the different primary antibodies and species-matched secondary antibodies. The bands were detected using enhanced chemiluminescence (Pierce) or the Odyssey Imaging System (LiCor Biosciences).
Xenograft study in nude mice
Three days after injection of estrogen in the abdomen (E2, 0.9 mg/kg, every three days), 5 × 106 MCF-7 cells were injected into the abdominal mammary fat pad of 4-week-old female nude mice. When tumor volume reached approximately 200 mm3, we randomly allocated the mice to groups in which they received PBS, metformin, tamoxifen, or a combination of the two drugs. Tumor growth was monitored by caliper measurements. Excised tumors were weighed, and portions were frozen in liquid nitrogen or fixed in 4% paraformaldehyde for further study.
Animal ethics statement
This study was performed in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the Forth Military Medical University. The protocol was approved by the Committee on the Ethics of Animal Experiments of the Forth Military Medical University. All surgery was performed under sodium pentobarbital anesthesia, and every effort was made to minimize suffering.
Immunohistochemical staining was performed as described previously  using rabbit anti-Ki67, anti-p-AMPK, anti-p-mTOR, and anti-p-p70S6 from Cell Signaling (Beverly, MA, USA) as primary antibodies.
Data from all quantitative assays are expressed as the mean ± standard deviation and were analyzed statistically using a one-way analysis of variance (ANOVA) and the independent-samples t test. Statistical calculations were performed using SPSS 14.0. P values of less than 0.05 were considered statistically significant.
Inhibition of the viability of ER-positive breast cancer cells by tamoxifen plus metformin
Inhibition of the DNA replication activity of ER-positive breast cancer cells by tamoxifen plus metformin
Inhibition of colony formation of ER-positive breast cancer cells by tamoxifen plus metformin
Promotion of apoptosis of ER-positive breast cancer cells by tamoxifen plus metformin
Activation of AMPK and inhibition of mTOR/p70S6 signaling by tamoxifen plus metformin
Metformin plus tamoxifen inhibit the growth of ER-positive breast cancer in vivo
Recently, the ATLAS clinical trial announced the latest results that continuing tamoxifen to 10 years rather than stopping at 5 years further reduces recurrence and mortality in patients with ER-positive breast cancer . This is encouraging news for the efficacy of tamoxifen, although its significant problems, therapeutic side-effects and resistance, must still be addressed. Some epidemiological studies suggest that metformin may exert anti-tumor effects in diabetic patients with breast cancer [10, 17]. Because of its minor side-effects and low toxicity, metformin may be a desirable drug for the prevention of breast cancers and the growth reduction of existing tumors in women [18–20]. However, the effects of metformin on endocrine therapies for ER-positive breast cancer patients are largely unknown. Based on this consideration, we investigated the efficacy of low-concentration doses of metformin alone or in combination with tamoxifen in a model of ER-positive breast cancer that reflects treatment strategies in common clinical use. In this study, we demonstrate that metformin enhanced the inhibitory effects of tamoxifen on the growth of ER-positive breast cancer in vitro and in vivo. Notably, when metformin was combined with tamoxifen, the concentration of tamoxifen required to inhibit growth was substantially reduced. Our observations indicate the potential importance of such combined approaches for increasing tamoxifen efficacy or lessening its side-effects in the clinical setting.
Metformin is widely used for the treatment of diabetes mellitus type 2, where it reduces insulin resistance and diabetes-related morbidity and mortality [8, 9]. Population-based studies show that metformin treatment is associated with a dose-dependent reduction in cancer risk [21, 22]. Metformin treatment also increases complete pathological tumor response rates following neoadjuvant chemotherapy for breast cancer, suggesting a potential role as an anti-cancer drug [23–25]. Diabetes mellitus type 2 is associated with insulin resistance, elevated insulin levels and an increased risk of cancer and cancer-related mortality [26, 27]. This increased risk may be explained by the activation of the insulin and insulin-like growth factor (IGF) signaling pathways and increased signaling through the estrogen receptor [28, 29]. Reversal of these processes through reduction of insulin resistance by the oral anti-diabetic drug metformin is an attractive anti-cancer strategy. In this study, we also provide direct evidence that metformin acts additively with endocrine therapy for ER-positive breast cancer patients, who account for almost 70% of all breast cancers. Metformin enhanced the inhibitory effects of tamoxifen on proliferation, DNA replication activity, colony formation, and soft-agar colony formation in ER-positive breast cancer cells. An increasing number of studies suggest that metformin is an activator of AMPK, which inhibits protein synthesis and gluconeogenesis during cellular stress [12–14]. The main downstream effect of AMPK activation is the inhibition of mTOR signaling pathways [13, 14]. Here we showed that in a time-dependent manner, metformin increased p-AMPK and decreased p-mTOR expression. p70S6, one of the critical downstream effectors of the mTOR signaling pathway, was also inhibited.
We found that the specific clinical circumstances in which metformin may be used in ER-positive breast cancer patients substantially influenced responsiveness to this agent. Our data are the first to examine the individual and combined effects of metformin and tamoxifen on a nude mouse model of ER-positive breast cancer and to investigate the apoptotic and growth pathways involved. Prior to this study, to our knowledge, there were two articles that described the effects of the combination of metformin and tamoxifen. One investigation suggested that metformin may decrease the density of endometrial glands and hyperplasia induced by tamoxifen in a mouse model . The other team found that metformin and tamoxifen inhibited the proliferation of MCF-7 cells and that tamoxifen-resistant cells were less sensitive to tamoxifen than to metformin . That study provided the important clue that metformin may exert an inhibitory effect on ER-positive breast cancer cells. It is consistent with our results that metformin and tamoxifen inhibit the growth of MCF-7 cells. The focus of our study was a wild-type, ER-positive breast cancer model, which represents patients receiving initial tamoxifen treatment. For these patients, it is possible that metformin additively augments tamoxifen efficacy but also suppresses tumor cell growth.
Taken together, our data indicate that metformin plus tamoxifen may have synergic effects on ER-positive breast cancer cells and tumor growth. We have further confirmed that these synergic effects of the two agents may be involved in the bax/bcl-2 apoptotic pathway and the AMPK/mTOR/p70S6 growth pathway. Although the antitumor effect of metformin is complicated and not yet fully understood, our findings provide direct evidence of its efficacy on ER-positive breast cancer in combination with tamoxifen treatment.
This work was supported by National Natural Science Foundation of China grants (NO. 81202085, 81202091, 81372478 and 81201209).
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