Xiong Yanlu, Wang Mingxing, Zhao Jinbo, Han Yong, Jia Lintao
Department of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, P.R. China.
State Key Laboratory of Cancer Biology, Department of Biochemistry and Molecular Biology, Fourth Military Medical University, Xi'an, Shaanxi 710032, P.R. China.
Int J Oncol. 2016 Dec;49(6):2227-2235. doi: 10.3892/ijo.2016.3767. Epub 2016 Nov 10.
The NAD-dependent protein deacetylase sirtuin 3 (SIRT3) is an enzyme localized primarily in the mitochondrion, where it modulates cellular functions such as nutrient metabolism, ATP balance, antioxidant machinery, and other mechanisms fundamental to mitochondria. SIRT3 is closely associated with the pathogenesis of diverse disorders. In particular, it plays a dual role in the development and progression of cancer. In many cancers, SIRT3 acts as an oncogene by promoting or maintaining the malignant phenotypes of neoplastic cells, including uncontrolled proliferation, resistance to apoptosis, and increased motility or invasiveness; however, SIRT3 suppresses these phenotypes in certain types of malignancy. The underlying mechanisms involve depletion of intracellular reactive oxygen species, modulation of metabolic reprogramming, and regulation of intracellular signaling responsible for cell growth and death. This review summarizes recent findings concerning the characteristics and substrates/interacting partners of SIRT3, with particular emphasis on emerging mechanisms responsible for fine-tuning cellular behaviors that potentially underlie its conflicting roles in carcinogenesis.
烟酰胺腺嘌呤二核苷酸(NAD)依赖性蛋白脱乙酰酶沉默调节蛋白3(SIRT3)是一种主要定位于线粒体的酶,它在其中调节细胞功能,如营养物质代谢、ATP平衡、抗氧化机制以及线粒体的其他基本机制。SIRT3与多种疾病的发病机制密切相关。特别是,它在癌症的发生和发展中发挥双重作用。在许多癌症中,SIRT3通过促进或维持肿瘤细胞的恶性表型,包括不受控制的增殖、对凋亡的抵抗以及运动性或侵袭性增加,而发挥癌基因的作用;然而,SIRT3在某些类型的恶性肿瘤中会抑制这些表型。其潜在机制包括细胞内活性氧的消耗、代谢重编程的调节以及负责细胞生长和死亡的细胞内信号传导的调节。本综述总结了关于SIRT3的特征及其底物/相互作用蛋白的最新发现,特别强调了负责微调细胞行为的新出现机制,这些机制可能是其在致癌作用中发挥矛盾作用的基础。