Zhao Di, Li Fu-Long, Cheng Zhou-Li, Lei Qun-Ying
Key Laboratory of Molecular Medicine; Ministry of Education, and Department of Biochemistry and Molecular Biology; Fudan University Shanghai Medical College; Shanghai, People's Republic of China; Molecular and Cell Biology Lab; Institutes of Biomedical Sciences; Fudan University; Shanghai, People's Republic of China.
Mol Cell Oncol. 2014 Oct 29;1(3):e963452. doi: 10.4161/23723548.2014.963452. eCollection 2014 Jul-Sep.
Acetylation of protein lysine residues is a reversible and dynamic process that is controlled by histone acetyltransferases (HATs) and deacetylases (HDACs and SIRTs). Recent studies have revealed that acetylation modulates not only nuclear proteins but also cytoplasmic or mitochondrial proteins, including many metabolic enzymes. In tumors, cellular metabolism is reprogrammed to provide intermediates for biosynthesis such as nucleotides, fatty acids, and amino acids, and thereby favor the rapid proliferation of cancer cells and tumor development. An increasing number of investigations have indicated that acetylation plays an important role in tumor metabolism. Here, we summarize the substrates that are modified by acetylation, especially oncogenes, tumor suppressor genes, and enzymes that are implicated in tumor metabolism.
蛋白质赖氨酸残基的乙酰化是一个可逆的动态过程,受组蛋白乙酰转移酶(HATs)和去乙酰化酶(HDACs和SIRTs)调控。最近的研究表明,乙酰化不仅调节核蛋白,还调节细胞质或线粒体蛋白,包括许多代谢酶。在肿瘤中,细胞代谢被重新编程,以提供生物合成所需的中间体,如核苷酸、脂肪酸和氨基酸,从而促进癌细胞的快速增殖和肿瘤发展。越来越多的研究表明,乙酰化在肿瘤代谢中起重要作用。在此,我们总结了被乙酰化修饰的底物,特别是癌基因、肿瘤抑制基因以及与肿瘤代谢相关的酶。