Saito Tsugumichi, Okada Shuichi, Yamada Eijiro, Shimoda Yoko, Osaki Aya, Tagaya Yuko, Shibusawa Ryo, Okada Junichi, Yamada Masanobu
Department of Medicine and Molecular Science, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan.
Endocr J. 2015;62(12):1133-7. doi: 10.1507/endocrj.EJ15-0396. Epub 2015 Oct 31.
Dapagliflozin is a SGLT2 (Sodium/Glucose cotransporter 2) inhibitor that reduces circulating glucose levels in type 2 diabetic patients by blocking the SGLT2-dependent reabsorption of glucose in the kidney. Dapagliflozin is metabolized by UGT1A9 (UDP Glucuronosyltransferase 1 family, Polypeptidase A9), suppressing its SGLT2 inhibitor activity. However little information is available on whether dapagliflozin acts in the absence of dapagliflozin metabolism. Treatment with 0.5μM dapagliflozin significantly reduced the number of HCT116 cells, which express SGLT2 but not UGT1A9. This was independent of SGLT2 inhibition, as the SGLT2 inhibitor phlorizin had no effect. Dapagliflozin also enhanced Erk phosphorylation but without changing levels of uncleaved and cleaved PPAR and uncleaved caspase-3, suggesting that the cause of the decrease in HCT116 cell number was apoptosis independent cell death. Taken together, these data indicate a new potential role for dapagliflozin as an anticancer reagent in tumor cell populations that do not express UGT1A9.
达格列净是一种钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂,通过阻断肾脏中依赖SGLT2的葡萄糖重吸收来降低2型糖尿病患者的循环血糖水平。达格列净由尿苷二磷酸葡萄糖醛酸基转移酶1A9(UGT1A9)代谢,从而抑制其SGLT2抑制剂活性。然而,关于达格列净在缺乏其代谢的情况下是否起作用的信息很少。用0.5μM达格列净处理可显著减少表达SGLT2但不表达UGT1A9的HCT116细胞数量。这与SGLT2抑制无关,因为SGLT2抑制剂根皮苷没有效果。达格列净还增强了细胞外信号调节激酶(Erk)的磷酸化,但未改变未切割和切割的过氧化物酶体增殖物激活受体(PPAR)以及未切割的半胱天冬酶-3的水平,这表明HCT116细胞数量减少的原因是凋亡非依赖性细胞死亡。综上所述,这些数据表明达格列净在不表达UGT1A9的肿瘤细胞群体中作为抗癌试剂具有新的潜在作用。