Zhuang Shan, Jian Yongmei, Sun Yongning
Department of Traditional Chinese Medicine, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Exp Clin Endocrinol Diabetes. 2017 Jun;125(6):392-399. doi: 10.1055/s-0043-100118. Epub 2017 Apr 13.
Type 2 diabetes can elevate risk of gastric cancer and metformin, an anti-diabetic agent, has an inhibitory effect against gastric cancer cell in vitro. However, the effect of metformin on type 2 diabetes-related gastric tumorigenesis in vivo is still not clear. In the present study, we aim to detect whether metformin can inhibit increased risk of gastric cancer in diabetic db/db mice and which the potential anti-cancer mechanisms of metformin are. 4-week-old mice were divided into 3 groups (2 db/db mice groups and one wild type mice group). All diabetic and non-diabetic mice were treated with N-Methyl-N-Nitrosourea (MNU) for 20 weeks to induce gastric tumorigenesis. At week 21, one db/db mice group were treated with metformin (5 mg/ml) for 10 weeks and the other 2 groups were treated with saline. Blood samples were collected for testing insulin and insulin-like growth factor (IGF)-1. Stomach tissues were collected for histopathological evaluation and mRNAs analysis. Metformin significantly decreased incidence of MNU-induced gastric dysplasia and cancer in diabetic db/db mice. Furthermore, metformin reduced serum insulin as well as IGF-1, and also suppressed expression of insulin receptor, IGF-1, IGF-1 receptor and several pro-inflammatory cytokines mRNAs in stomach of db/db mice, but did not significantly influence IGF-2 and IGF-2 receptor expressions. The results show that metformin can prevent the risk of gastric cancer in type 2 diabetes and the protective mechanisms may involve in an inhibitory effect of metformin on insulin as well as IGF-1 signals and cancer related pro-inflammatory cytokines.
2型糖尿病会增加患胃癌的风险,而抗糖尿病药物二甲双胍在体外对胃癌细胞具有抑制作用。然而,二甲双胍对2型糖尿病相关胃癌发生的体内影响仍不清楚。在本研究中,我们旨在检测二甲双胍是否能抑制糖尿病db/db小鼠胃癌风险的增加,以及二甲双胍潜在的抗癌机制是什么。将4周龄的小鼠分为3组(2组db/db小鼠和1组野生型小鼠)。所有糖尿病和非糖尿病小鼠均用N-甲基-N-亚硝基脲(MNU)处理20周以诱导胃癌发生。在第21周,一组db/db小鼠用二甲双胍(5mg/ml)处理10周,另外2组用生理盐水处理。采集血样检测胰岛素和胰岛素样生长因子(IGF)-1。采集胃组织进行组织病理学评估和mRNA分析。二甲双胍显著降低了糖尿病db/db小鼠中MNU诱导的胃发育异常和癌症的发生率。此外,二甲双胍降低了血清胰岛素以及IGF-1水平,还抑制了db/db小鼠胃中胰岛素受体、IGF-1、IGF-1受体和几种促炎细胞因子mRNA的表达,但对IGF-2和IGF-2受体的表达没有显著影响。结果表明,二甲双胍可以预防2型糖尿病患者患胃癌的风险,其保护机制可能涉及二甲双胍对胰岛素以及IGF-1信号和癌症相关促炎细胞因子的抑制作用。