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Metformin kills and radiosensitizes cancer cells and preferentially kills cancer stem cells

机译:二甲双胍可杀死癌细胞并使其放射增敏并优先杀死癌细胞干细胞

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摘要

The anti-cancer effects of metformin, the most widely used drug for type 2 diabetes, alone or in combination with ionizing radiation were studied with MCF-7 human breast cancer cells and FSaII mouse fibrosarcoma cells. Clinically achievable concentrations of metformin caused significant clonogenic death in cancer cells. Importantly, metformin was preferentially cytotoxic to cancer stem cells relative to non-cancer stem cells. Metformin increased the radiosensitivity of cancer cells in vitro, and significantly enhanced the radiation-induced growth delay of FSaII tumors (s.c.) in the legs of C3H mice. Both metformin and ionizing radiation activated AMPK leading to inactivation of mTOR and suppression of its downstream effectors such as S6K1 and 4EBP1, a crucial signaling pathway for proliferation and survival of cancer cells, in vitro as well as in the in vivo tumors. Conclusion: Metformin kills and radiosensitizes cancer cells and eradicates radioresistant cancer stem cells by activating AMPK and suppressing mTOR.
机译:使用MCF-7人乳腺癌细胞和FSaII小鼠纤维肉瘤细胞研究了二甲双胍(一种最广泛使用的2型糖尿病药物)的单独或与电离辐射联合使用的抗癌作用。临床上可达到的二甲双胍浓度在癌细胞中引起明显的克隆形成性死亡。重要的是,相对于非癌干细胞,二甲双胍优先对癌干细胞具有细胞毒性。二甲双胍增加了体外癌细胞的放射敏感性,并显着增强了C3H小鼠腿部FSaII肿瘤(s.c.)的辐射诱导生长延迟。二甲双胍和电离辐射均激活AMPK,从而导致mTOR失活并抑制其下游效应物,例如S6K1和4EBP1,这是癌细胞在体外和体内肿瘤中增殖和存活的关键信号途径。结论:二甲双胍可通过激活AMPK和抑制mTOR来杀死癌细胞并使其放射增敏,并消除具有放射线敏感性的癌症干细胞。

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