Even Cancer Cells Watch Their Cholesterol!

被引:157
作者
Riscal, Romain [1 ]
Skuli, Nicolas [1 ]
Simon, M. Celeste [1 ,2 ]
机构
[1] Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
INDUCE CYCLOOXYGENASE-2 EXPRESSION; FATTY-ACID SYNTHESIS; BILE-ACIDS; LIPID-METABOLISM; 27-HYDROXYCHOLESTEROL PROMOTES; MEVALONATE PATHWAY; RECEPTOR LXR; STATIN USE; SR-BI; 24-HYDROXYCHOLESTEROL;
D O I
10.1016/j.molcel.2019.09.008
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
Deregulated cell proliferation is an established feature of cancer, and altered tumor metabolism has witnessed renewed interest over the past decade, including the study of how cancer cells rewire metabolic pathways to renew energy sources and "building blocks'' that sustain cell division. Microenvironmental oxygen, glucose, and glutamine are regarded as principal nutrients fueling tumor growth. However, hostile tumor microenvironments render O-2/nutrient supplies chronically insufficient for increased proliferation rates, forcing cancer cells to develop strategies for opportunistic modes of nutrient acquisition. Recent work shows that cancer cells overcome this nutrient scarcity by scavenging other substrates, such as proteins and lipids, or utilizing adaptive metabolic pathways. As such, reprogramming lipid metabolism plays important roles in providing energy, macromolecules for membrane synthesis, and lipid-mediated signaling during cancer progression. In this review, we highlight more recently appreciated roles for lipids, particularly cholesterol and its derivatives, in cancer cell metabolism within intrinsically harsh tumor microenvironments.
引用
收藏
页码:220 / 231
页数:12
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