Metabolic regulation by SIRT3: implications for tumorigenesis.

Abstract:

:Cancer cells meet their needs for energy and biomass production by consuming high levels of nutrients and rewiring metabolism to support macromolecular biosynthesis. Mitochondrial enzymes play central roles in anabolic growth, and acetylation may provide a key layer of regulation over mitochondrial metabolic pathways. As a major mitochondrial deacetylase, SIRT3 regulates the activity of enzymes to coordinate global shifts in cellular metabolism. SIRT3 promotes the function of the tricarboxylic acid (TCA) cycle and the electron transport chain and reduces oxidative stress. Loss of SIRT3 triggers oxidative damage, reactive oxygen species (ROS)-mediated signaling, and metabolic reprogramming to support proliferation and tumorigenesis. Thus, SIRT3 is an intriguing example of how nutrient-sensitive, post-translational regulation may provide integrated regulation of metabolic pathways to promote metabolic homeostasis in response to diverse nutrient signals.

journal_name

Trends Mol Med

authors

Finley LW,Haigis MC

doi

10.1016/j.molmed.2012.05.004

subject

Has Abstract

pub_date

2012-09-01 00:00:00

pages

516-23

issue

9

eissn

1471-4914

issn

1471-499X

pii

S1471-4914(12)00080-9

journal_volume

18

pub_type

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