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首页> 外文期刊>Oncology reports >Metformin inhibits proliferation and enhances chemosensitivity of intrahepatic cholangiocarcinoma cell lines
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Metformin inhibits proliferation and enhances chemosensitivity of intrahepatic cholangiocarcinoma cell lines

机译:二甲双胍抑制肝内胆管癌细胞系的增殖并增强其化学敏感性

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摘要

Metformin is an oral anti-hyperglycemic agent of the biguanide family, which is used first-line for type II diabetes with few side-effects. A recent epidemiological study that included 1,828 potential intrahepatic cholangiocarcinoma (ICC) patients showed that metformin use was significantly associated with a 60% reduction in ICC risk in diabetic patients, demonstrating the potential value of metformin in ICC management. In the present study, we firstly showed that metformin exhibited a dose- and time-dependent anti-proliferation effect on ICC cell lines, by mechanisms including apoptosis induction and cell cycle arrest. Metformin targeted the AMPK/mTORC1 pathway in ICC cells. Furthermore, metformin sensitized ICC cells to certain chemotherapeutic agents, such as sorafenib, 5-fluorouracil and As2O3 by targeting the AMPK/mTOR/HIF-1 alpha/MRP1 pathway and ERK. As it is an inexpensive and widely used antidiabetic drug without severe adverse effects, metformin may be a prospective chemotherapeutic agent or a chemosensitizer in future ICC treatment.
机译:二甲双胍是双胍类的口服抗高血糖药,被用于一线治疗II型糖尿病且副作用很小。最近的一项流行病学研究包括1,828例潜在的肝内胆管癌(ICC)患者,显示二甲双胍的使用与糖尿病患者ICC风险降低60%显着相关,证明了二甲双胍在ICC管理中的潜在价值。在本研究中,我们首先表明二甲双胍通过包括细胞凋亡诱导和细胞周期停滞在内的机制对ICC细胞系表现出剂量和时间依赖性的抗增殖作用。二甲双胍靶向ICC细胞中的AMPK / mTORC1途径。此外,二甲双胍通过靶向AMPK / mTOR / HIF-1 alpha / MRP1途径和ERK,使ICC细胞对某些化学治疗剂(如索拉非尼,5-氟尿嘧啶和As2O3)敏感。由于二甲双胍是一种廉价且广泛使用的抗糖尿病药,没有严重的副作用,因此在未来的ICC治疗中,二甲双胍可能是前瞻性化学治疗剂或化学增敏剂。

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