Aberrant lipid metabolism in cancer cells - the role of oncolipid-activated signaling

被引:70
|
作者
Ray, Upasana [1 ]
Roy, Sib Sankar [1 ]
机构
[1] CSIR, Indian Inst Chem Biol, Cell Biol & Physiol Div, 4 Raja SC Mullick Rd, Kolkata 700032, India
关键词
cancer; lipid metabolism; lysophosphatidic acid; metabolic reprogramming; FATTY-ACID SYNTHASE; STEAROYL-COA DESATURASE; DE-NOVO LIPOGENESIS; LYSOPHOSPHATIDIC ACID; PROSTATE-CANCER; SYNTHESIS PATHWAY; OVARIAN; EXPRESSION; INHIBITION; TARGET;
D O I
10.1111/febs.14281
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
Metabolic activity of malignant cells is very different from that of their nontransformed equivalents, which establishes metabolic reprogramming as an important hallmark of every transformed cell. In particular, the current arena of research in this field aims to understand the regulatory effect of oncogenic signaling on metabolic rewiring in transformed cells in order to exploit this for therapeutic benefit. Alterations in lipid metabolism are one of the main aspects of metabolic rewiring of transformed cells. Up-regulation ofseveral lipogenic enzymes has been reported to be a characteristic of various cancer types. Lysophosphatidic acid (LPA), a simple byproduct of the lipid biosynthesis pathway, has gained immense importance due to its elevated level in several cancers and associated growth-promoting activity. Importantly, a current study revealed its role in increased denovo lipid synthesis through up-regulation of sterol regulatory element-binding protein 1, a master regulator of lipid metabolism. This review summarizes the recent insights in the field of oncolipid LPA-mediated signaling in regard to lipid metabolism in cancers. Future work in this domain is required to understand the up-regulation of the denovo synthesis pathway and the role of its end products in malignant cells. This will open a new arena of research toward the development of specific metabolic inhibitors that can add to the pre-existing chemotherapeutics in order to increase the efficacy of clinical output in cancer patients.
引用
收藏
页码:432 / 443
页数:12
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