Second Medical Oncology Unit, Istituto Oncologico Veneto, Padua, Italy;
Oncologist. 2013;18(10):1118-25. doi: 10.1634/theoncologist.2013-0177. Epub 2013 Sep 16.
Type 2 diabetes mellitus patients are at higher cancer risk, probably because of hyperinsulinemia and insulin growth factor 1 pathway activation. The effects of antidiabetic drugs on cancer risk have been described and discussed in several studies suggesting opposite effects of the biguanide metformin and sulfonylureas on cancer incidence and mortality. The anticancer mechanisms of metformin have been clarified, and some clinical studies, particularly in breast cancer patients, have been published or are currently ongoing; however, data about the effects of sulfonylureas on cancer growth are less consistent. The aims of this work are to review preclinical evidence of second-generation sulfonylureas effects on tumor growth, to clarify the potential mechanisms of action, and to identify possible metabolic targets for patient selection. Most evidence is on the adenosine triphosphate-sensitive potassium channels inhibitor glibenclamide, which interacts with reactive oxygen species production thus inducing cancer cell death. Among diarylsulfonylureas, next-generation DW2282 derivatives are particularly promising because of the proapoptotic activity in multidrug-resistant cells.
2 型糖尿病患者的癌症风险较高,这可能是由于高胰岛素血症和胰岛素生长因子 1 通路的激活。一些研究描述和讨论了抗糖尿病药物对癌症风险的影响,表明双胍类药物二甲双胍和磺酰脲类药物对癌症发病率和死亡率的影响相反。二甲双胍的抗癌机制已经阐明,一些临床研究,特别是在乳腺癌患者中,已经发表或正在进行中;然而,磺酰脲类药物对癌症生长影响的数据则不太一致。这项工作的目的是回顾第二代磺酰脲类药物对肿瘤生长影响的临床前证据,阐明潜在的作用机制,并确定可能的代谢靶点以选择患者。大多数证据都集中在三磷酸腺苷敏感的钾通道抑制剂格列本脲上,它与活性氧的产生相互作用,从而诱导癌细胞死亡。在二苯磺酰脲类中,新一代 DW2282 衍生物由于在多药耐药细胞中的促凋亡活性而特别有前景。