Stearoyl-CoA desaturase and tumorigenesis

被引:41
|
作者
Kikuchi, Kohtaro
Tsukamoto, Hidekazu
机构
[1] Univ Southern Calif, Keck Sch Med, Southern Calif Res Ctr ALPD & Cirrhosis, Los Angeles, CA 90007 USA
[2] Univ Southern Calif, Keck Sch Med, Dept Pathol, Los Angeles, CA 90007 USA
基金
美国国家卫生研究院;
关键词
Hepatic stellate cells; Wnt; beta-catenin; YAP; MONOUNSATURATED FATTY-ACIDS; GENE-EXPRESSION PROFILE; BETA-CATENIN; PROTECTS MICE; CANCER-CELLS; LIVER; DEFICIENCY; INHIBITION; KINASE; STEAROYL-COA-DESATURASE-1;
D O I
10.1016/j.cbi.2019.108917
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stearoyl-CoA desaturase (SCD) generates monounsaturated fatty acids (MUFAs) which contribute to cell growth, survival, differentiation, metabolic regulation and signal transduction. Overexpression of SCD is evident and implicated in metabolic diseases such as diabetes and non-alcoholic fatty liver disease. SCD also stimulates canonical Wnt pathway and YAP activation in support of stemness and tumorigenesis. SCD facilitates metabolic reprogramming in cancer which is mediated, at least in part, by regulation of AKT, AMPK, and NF-kB via MUFAs. Our research has revealed the novel positive loop to amplify Wnt signaling through stabilization of LRP5/6 in both hepatic stellate cells and liver tumor-initiating stem cell-like cells. As such, this loop is pivotal in promoting liver fibrosis and liver tumor development. This review summarizes the mechanisms of SCD-mediated tumor promotion described by recent studies and discusses the future prospect for SCD-mediated signaling crosstalk as a potential therapeutic target for cancer.
引用
收藏
页数:6
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