癌细胞
细胞生长
基因沉默
癌症研究
生物
下调和上调
细胞
代谢组学
生物化学
脂肪酸合成
化学
脂类学
细胞生物学
脂肪酸
癌症
基因
生物信息学
遗传学
作者
Zachary T. Schug,Barrie Peck,Dylan T. Jones,Zuo‐Feng Zhang,Shaun Grosskurth,Israt S. Alam,Louise Goodwin,Elizabeth A. Smethurst,Susan Mason,Karen Blyth,Lynn McGarry,Daniel James,Emma Shanks,Gabriela Kalna,Rebecca E. Saunders,Ming Jiang,Michael Howell,François Lassailly,May Zaw Thin,Bradley Spencer‐Dene
出处
期刊:Cancer Cell
[Cell Press]
日期:2015-01-01
卷期号:27 (1): 57-71
被引量:798
标识
DOI:10.1016/j.ccell.2014.12.002
摘要
A functional genomics study revealed that the activity of acetyl-CoA synthetase 2 (ACSS2) contributes to cancer cell growth under low-oxygen and lipid-depleted conditions. Comparative metabolomics and lipidomics demonstrated that acetate is used as a nutritional source by cancer cells in an ACSS2-dependent manner, and supplied a significant fraction of the carbon within the fatty acid and phospholipid pools. ACSS2 expression is upregulated under metabolically stressed conditions and ACSS2 silencing reduced the growth of tumor xenografts. ACSS2 exhibits copy-number gain in human breast tumors, and ACSS2 expression correlates with disease progression. These results signify a critical role for acetate consumption in the production of lipid biomass within the harsh tumor microenvironment.
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