College of Pharmacy, Woosuk University, 443 Samnye-ro, Wanju, Jeonbuk, 55338, Republic of Korea.
Arch Pharm Res. 2017 Dec;40(12):1380-1389. doi: 10.1007/s12272-017-0989-8. Epub 2017 Nov 25.
Sirtuin 6 (SIRT6), one of the seven members of mammalian sirtuin family, localizes in the nucleus and primarily regulates chromatin signaling and genomic integrity. Recent studies established the critical role of SIRT6 in the pathophysiology of metabolic disease, as well as its roles in longevity and cancer. These roles that were determined by genetic studies include promoting pancreatic insulin secretion, inhibiting hepatic gluconeogenesis and triglyceride synthesis, and suppressing adiposity, suggesting that SIRT6 activators are promising molecules for treating obesity and diabetes. In contrast, a recent study showed that a synthetic inhibitor of SIRT6 improved glucose tolerance in a type 2 diabetes mouse model, associated with increased glycolysis and the expression of glucose transporter GLUT-1 and 4 in skeletal muscle, providing proof-of-concept evidence of SIRT6 inhibition as a treatment for diabetes. This review summarizes the confounding findings on the role of SIRT6 in metabolic homeostasis and discusses the possible relationships of these findings as they relate to the use of SIRT6 as a therapeutic target for type 2 diabetes and related diseases.
Sirtuin 6(SIRT6)是哺乳动物 Sirtuin 家族的七个成员之一,定位于细胞核内,主要调节染色质信号和基因组完整性。最近的研究确立了 SIRT6 在代谢性疾病的病理生理学中的关键作用,以及它在长寿和癌症中的作用。这些通过遗传研究确定的作用包括促进胰腺胰岛素分泌、抑制肝糖异生和甘油三酯合成、抑制脂肪堆积,这表明 SIRT6 激活剂是治疗肥胖症和糖尿病的有前途的分子。相比之下,最近的一项研究表明,SIRT6 的一种合成抑制剂可改善 2 型糖尿病小鼠模型的葡萄糖耐量,与骨骼肌中糖酵解和葡萄糖转运蛋白 GLUT-1 和 4 的表达增加相关,为 SIRT6 抑制作为治疗糖尿病的一种方法提供了概念验证证据。这篇综述总结了 SIRT6 在代谢稳态中的作用的令人困惑的发现,并讨论了这些发现与将 SIRT6 作为 2 型糖尿病及相关疾病的治疗靶点的可能关系。