Lipid metabolism reprogramming and its potential targets in cancer

被引:564
作者
Cheng, Chunming
Geng, Feng
Cheng, Xiang
Guo, Deliang [1 ]
机构
[1] Ohio State Univ, James Comprehens Canc Ctr, Dept Radiat Oncol, Columbus, OH 43210 USA
关键词
Lipid metabolism; Cancer; SCAP; SREBPs; Fatty acids; Cholesterol; Lipid droplets; FATTY-ACID SYNTHASE; ATP-CITRATE-LYASE; ELEMENT-BINDING PROTEIN; LIVER X RECEPTOR; COA-DESATURASE; PROMOTES GENE-TRANSCRIPTION; LEUCINE ZIPPER PROTEIN; PROSTATE-CANCER; BREAST-CANCER; CELL-GROWTH;
D O I
10.1186/s40880-018-0301-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Reprogramming of lipid metabolism is a newly recognized hallmark of malignancy. Increased lipid uptake, storage and lipogenesis occur in a variety of cancers and contribute to rapid tumor growth. Lipids constitute the basic structure of membranes and also function as signaling molecules and energy sources. Sterol regulatory element-binding proteins (SREBPs), a family of membrane-bound transcription factors in the endoplasmic reticulum, play a central role in the regulation of lipid metabolism. Recent studies have revealed that SREBPs are highly up-regulated in various cancers and promote tumor growth. SREBP cleavage-activating protein is a key transporter in the trafficking and activation of SREBPs as well as a critical glucose sensor, thus linking glucose metabolism and de novo lipid synthesis. Targeting altered lipid metabolic pathways has become a promising anti-cancer strategy. This review summarizes recent progress in our understanding of lipid metabolism regulation in malignancy, and highlights potential molecular targets and their inhibitors for cancer treatment.
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页数:14
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