Zi Fuming, Zi Huapu, Li Yi, He Jingsong, Shi Qingzhi, Cai Zhen
Department of Hematology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330008, P.R. China.
Department of Oncology, Rizhao Traditional Chinese Medicine Hospital of Shandong Traditional Chinese Medicine University, Rizhao, Shandong 276800, P.R. China.
Oncol Lett. 2018 Jan;15(1):683-690. doi: 10.3892/ol.2017.7412. Epub 2017 Nov 14.
Metformin is a standard clinical drug used to treat type 2 diabetes mellitus (T2DM) and polycystic ovary syndrome. Recently, epidemiological studies and meta-analyses have revealed that patients with T2DM have a lower incidence of tumor development than healthy controls and that patients diagnosed with cancer have a lower risk of mortality when treated with metformin, demonstrating an association between metformin and tumorigenesis. and studies have revealed that metformin has a direct antitumor effect, which may depress tumor proliferation and induce the apoptosis, autophagy and cell cycle arrest of tumor cells. The mechanism underpinning the antitumor effect of metformin has not been well established. Studies have demonstrated that reducing insulin and insulin-like growth factor levels in the peripheral blood circulation may lead to the inhibition of phosphoinositide 3-kinase/Akt/mechanistic target of rapamycin (mTOR) signaling or activation of AMP-activated protein kinase, which inhibits mTOR signaling, a process that may be associated with the antitumor effect of metformin. The present review primarily focuses on the recent progress in understanding the function of metformin in tumor development.
二甲双胍是一种用于治疗2型糖尿病(T2DM)和多囊卵巢综合征的标准临床药物。最近,流行病学研究和荟萃分析表明,T2DM患者的肿瘤发生发生率低于健康对照,并且被诊断患有癌症的患者在接受二甲双胍治疗时死亡风险较低,这表明二甲双胍与肿瘤发生之间存在关联。 研究表明,二甲双胍具有直接的抗肿瘤作用,可能会抑制肿瘤增殖并诱导肿瘤细胞的凋亡、自噬和细胞周期停滞。二甲双胍抗肿瘤作用的潜在机制尚未完全明确。研究表明,降低外周血液循环中的胰岛素和胰岛素样生长因子水平可能导致磷酸肌醇3-激酶/蛋白激酶B/雷帕霉素机制性靶标(mTOR)信号传导的抑制或AMP激活的蛋白激酶的激活,从而抑制mTOR信号传导,这一过程可能与二甲双胍的抗肿瘤作用有关。本综述主要关注在理解二甲双胍在肿瘤发生中的作用方面的最新进展。