Febbraro Terri, Lengyel Ernst, Romero Iris L
Department of Obstetrics and Gynecology, University of Chicago, Chicago, IL, USA.
Department of Obstetrics and Gynecology, University of Chicago, Chicago, IL, USA.
Gynecol Oncol. 2014 Dec;135(3):614-21. doi: 10.1016/j.ygyno.2014.10.011. Epub 2014 Oct 23.
There is increasing pre-clinical and clinical evidence that metformin, a commonly used diabetes medication, has a protective effect in cancer. The aim of this review is to discuss metformin's anti-cancer molecular mechanisms of action and to summarize the current literature demonstrating metformin's potential in gynecologic cancer prevention and treatment.
A PubMed search was conducted combining the keywords "metformin" with "neoplasm", "uterine neoplasms", "ovarian neoplasms", and "uterine cervical neoplasms". Studies published in English between 1994 and 2014 were included.
Pre-clinical studies in endometrial, ovarian, and cervical cancer suggest that metformin inhibits the growth of cancer cells. The primary molecular mechanism mediating this effect appears to be the activation of AMP-activated protein kinase (AMPK) and the subsequent inhibition of mammalian targets of rapamycin (mTOR). The pre-clinical findings are augmented by clinical studies indicating that metformin use is associated with a reduced risk of cancer and improved survival in diabetic women with ovarian and endometrial cancers. No clinical analyses have evaluated metformin use and cervical cancer. Overall, the data showing a favorable effect of metformin is strongest for endometrial and ovarian cancer and prospective clinical testing is ongoing in these two malignancies.
Numerous clinical studies have reported an association between metformin use by diabetic patients and improved outcomes in gynecologic cancers. In addition, pre-clinical reports have identified plausible biological mechanisms to explain the molecular mechanism of action of metformin in cancer. However, the most important question remains unanswered: Will metformin be effective against cancer in patients without diabetes? Until this question is answered with prospective clinical testing, the role of metformin in the treatment or prevention of gynecologic malignancies remains theoretical and the clinical use of metformin as a cancer therapeutic is experimental.
越来越多的临床前和临床证据表明,常用的糖尿病药物二甲双胍对癌症具有保护作用。本综述的目的是探讨二甲双胍的抗癌分子作用机制,并总结目前证明二甲双胍在妇科癌症预防和治疗中潜力的文献。
在PubMed上进行搜索,将关键词“二甲双胍”与“肿瘤”、“子宫肿瘤”、“卵巢肿瘤”和“子宫颈肿瘤”相结合。纳入1994年至2014年期间以英文发表的研究。
子宫内膜癌、卵巢癌和宫颈癌的临床前研究表明,二甲双胍可抑制癌细胞生长。介导这种作用的主要分子机制似乎是激活AMP活化蛋白激酶(AMPK),随后抑制雷帕霉素的哺乳动物靶点(mTOR)。临床研究进一步证实了临床前研究结果,这些研究表明,使用二甲双胍与降低癌症风险以及改善患有卵巢癌和子宫内膜癌的糖尿病女性的生存率相关。尚无临床分析评估二甲双胍的使用与宫颈癌之间的关系。总体而言,显示二甲双胍具有有益作用的数据在子宫内膜癌和卵巢癌方面最为有力,并正在对这两种恶性肿瘤进行前瞻性临床试验。
许多临床研究报告了糖尿病患者使用二甲双胍与妇科癌症预后改善之间的关联。此外,临床前报告已经确定了合理的生物学机制来解释二甲双胍在癌症中的分子作用机制。然而,最重要的问题仍然没有答案:二甲双胍对非糖尿病患者的癌症是否有效?在这个问题通过前瞻性临床试验得到解答之前,二甲双胍在治疗或预防妇科恶性肿瘤中的作用仍然是理论性的,将二甲双胍作为癌症治疗药物的临床应用仍处于实验阶段。