脂质代谢
脂肪生成
过氧化物酶体增殖物激活受体
癌细胞
细胞生物学
过氧化物酶体
转录因子
脂滴
肿瘤微环境
生物
癌症
受体
医学
生物化学
内科学
基因
作者
Yunkuo Li,Yujie Pan,Xiaodong Zhao,Shouwang Wu,Faping Li,Yuxiong Wang,Bin Liu,Yanghe Zhang,Xin Gao,Yishu Wang,Honglan Zhou
标识
DOI:10.1016/j.clnu.2023.12.005
摘要
Lipids represent the essential components of membranes, serve as fuels for high-energy processes, and play crucial roles in signaling and cellular function.One of the key hallmarks of cancer is the reprogramming of metabolic pathways, especially abnormal lipid metabolism.Alterations in lipid uptake, lipid desaturation, de novo lipogenesis, lipid droplets, and fatty acid oxidation in cancer cells all contribute to cell survival in a changing microenvironment by regulating feedforward oncogenic signals, key oncogenic functions, oxidative and other stresses, immune responses, or intercellular communication.Peroxisome proliferator-activated receptors (PPARs) are transcription factors activated by fatty acids and act as core lipid sensors involved in the regulation of lipid homeostasis and cell fate.In addition to regulating whole-body energy homeostasis in physiological states, PPARs play a key role in lipid metabolism in cancer, which is receiving increasing research attention, especially the fundamental molecular mechanisms and cancer therapies targeting PPARs.In this review, we discuss how cancer cells alter metabolic patterns and regulate lipid metabolism to promote their own survival and progression through PPARs.Finally, we discuss potential therapeutic strategies for targeting PPARs in cancer based on recent studies from the last five years.
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