Chen Xu, Hu Chuanzhen, Zhang Weibin, Shen Yuhui, Wang Jun, Hu Fangqiong, Yu Pei
Shanghai Key Laboratory for Prevention and Treatment of Bone and joint Diseases with Integrated Chinese-Western Medicine, Shanghai Institute of Orthopedics and Traumatology, Shanghai, 20025, People's Republic of China.
Department of Orthopaedics, Ruijin Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, 20025, People's Republic of China.
Tumour Biol. 2015 Dec;36(12):9873-83. doi: 10.1007/s13277-015-3751-1. Epub 2015 Jul 13.
Metformin is an oral drug that has been widely used to treat type 2 diabetes mellitus. Interestingly, accumulated evidence indicate that metformin may reduce the risk of cancer in patients with type 2 diabetes and inhibit tumor cell growth and survival in numerous malignancies, including osteosarcoma (OS) cells. In the present study, we aimed to investigate the effects of metformin on the proliferation, migration, invasion, and sphere formation in OS MG63 cells in vitro. Metformin suppressed OS MG63 cell proliferation in a dose- and time-dependent manner and markedly blocked anti-metastatic potentials, migration, and invasion, by downregulating matrix metalloproteinase 2 (MMP2) and MMP9. Besides, we established OS cancer stem-like cell (CSC) model with sarcosphere formation assay and demonstrated that metformin posed damage on CSCs in OS by inhibiting sphere formation and by inducing their stemness loss. The stemness of CSCs in OS such as self-renewal and differentiation potentials was both impaired with a significant decrease of Oct-4 and Nanog activation. Consistent with this, the positive rates of CD90, CD133, and stage-specific embryonic antigen-4 (SSEA-4) were all observed with reductions in response to metformin exposure. In addition, Western blot showed that metformin activated AMPKα at Tyr172, followed by a downregulated phosphorylation of mammalian target of rapamycin (mTOR)/S6 and feedback activation of p-AKT Ser(473) in both OS MG63 cells and CSCs. This indicates that AMPK/mTOR/S6 signaling pathway might be involved in the growth inhibition of both OS MG63 cells and CSCs. These results suggest that metformin, a potential anti-neoplastic agent, might make it a novel therapeutic choice for the treatment of OS in the future.
二甲双胍是一种口服药物,已被广泛用于治疗2型糖尿病。有趣的是,越来越多的证据表明,二甲双胍可能降低2型糖尿病患者患癌风险,并抑制包括骨肉瘤(OS)细胞在内的多种恶性肿瘤的肿瘤细胞生长和存活。在本研究中,我们旨在探讨二甲双胍对体外培养的OS MG63细胞增殖、迁移、侵袭和球状体形成的影响。二甲双胍以剂量和时间依赖性方式抑制OS MG63细胞增殖,并通过下调基质金属蛋白酶2(MMP2)和MMP9显著阻断其抗转移潜能、迁移和侵袭。此外,我们通过球状体形成试验建立了OS癌干细胞(CSC)模型,并证明二甲双胍通过抑制球状体形成和诱导其干性丧失对OS中的CSC造成损伤。OS中CSC的干性,如自我更新和分化潜能均受损,Oct-4和Nanog激活显著降低。与此一致的是,观察到CD90、CD133和阶段特异性胚胎抗原-4(SSEA-4)的阳性率在二甲双胍处理后均降低。此外,蛋白质印迹显示,二甲双胍在Tyr172位点激活AMPKα,随后在OS MG63细胞和CSC中下调雷帕霉素靶蛋白(mTOR)/S6的磷酸化,并反馈激活p-AKT Ser(473)。这表明AMPK/mTOR/S6信号通路可能参与了对OS MG63细胞和CSC的生长抑制。这些结果表明,二甲双胍作为一种潜在的抗肿瘤药物,可能在未来成为治疗OS的一种新型治疗选择。