Metformin and cancer: new applications for an old drug

被引:288
作者
Kourelis, Taxiarchis V. [1 ]
Siegel, Robert D. [2 ]
机构
[1] Univ Connecticut, Sch Med, Dept Med, Farmington, CT 06103 USA
[2] Hartford Hosp, Canc Clin Res Off, Div Med Oncol, Hartford, CT 06106 USA
关键词
Metformin; Cancer; mTOR; LKB1; AMPK; Insulin; Diabetes; ACTIVATED PROTEIN-KINASE; MESENCHYMAL TRANSITION EMT; CELL-CYCLE ARREST; BREAST-CANCER; PANCREATIC-CANCER; DIABETES-MELLITUS; MAMMALIAN TARGET; AMPK ACTIVATOR; FACTOR-I; RISK;
D O I
10.1007/s12032-011-9846-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Metformin, one of most widely prescribed oral hypoglycemic agents, has recently received increased attention because of its potential antitumorigenic effects that are thought to be independent of its hypoglycemic effects. Several potential mechanisms have been suggested for the ability of metformin to suppress cancer growth in vitro and vivo: (1) activation of LKB1/AMPK pathway, (2) induction of cell cycle arrest and/or apoptosis, (3) inhibition of protein synthesis, (4) reduction in circulating insulin levels, (5) inhibition of the unfolded protein response (UPR), (6) activation of the immune system, and (7) eradication of cancer stem cells. There is also a growing number of evidence, mostly in the form of retrospective clinical studies that suggest that metformin may be associated with a decreased risk of developing cancer and with a better response to chemotherapy. There are currently several ongoing randomized clinical trials that incorporate metformin as an adjuvant to classic chemotherapy and aim to evaluate its potential benefits in this setting. This review highlights basic aspects of the molecular biology of metformin and summarizes new advances in basic science as well as intriguing results from recent clinical studies.
引用
收藏
页码:1314 / 1327
页数:14
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