Mammalian Sirtuins: Biological Insights and Disease Relevance

被引:1668
作者
Haigis, Marcia C. [1 ]
Sinclair, David A. [1 ]
机构
[1] Harvard Univ, Sch Med, Glen Labs Mol Biol Aging, Dept Pathol, Boston, MA 02115 USA
关键词
chromatin; metabolism; deacetylase; cancer; cardiovascular; inflammation; LIFE-SPAN EXTENSION; NF-KAPPA-B; FOXO TRANSCRIPTION FACTORS; SMALL-MOLECULE ACTIVATORS; NAD(+) SALVAGE PATHWAY; PANCREATIC BETA-CELLS; DNA-DAMAGE RESPONSE; STIMULATED INSULIN-SECRETION; SIRT1-NULL MICE DEVELOP; HUMAN ENDOTHELIAL-CELLS;
D O I
10.1146/annurev.pathol.4.110807.092250
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aging is accompanied by a decline in the healthy function of multiple organ systems, leading to increased incidence and mortqlity from diseases such as type U diabetes mellitus, neurodegenerative diseases, cancer, and cardiovascular disease. Historically, researchers have focused on investigating individual pathways in isolated organs as a strategy to identify the root Cause Of a disease, with hopes of designing better drugs. Studies of aging in yeast led to the discovery of a family of conserved enzymes known as the sirtuins, which affect multiple pathways that increase the life span and the overall health of organisms. Since the discovery of the first known mammalian sirtuin, SIRT1, 10 years ago, there have been major advances in our understanding of the enzymology of sirtuins, their regulation, and their ability to broadly improve mammalian physiology and health span. This review summarizes and discusses the advances of the past decade and the challenges that will confront the field in the coming years.
引用
收藏
页码:253 / 295
页数:43
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