Therapeutic potential of lipin inhibitors for the treatment of cancer

磷脂酸 二酰甘油激酶 癌症 生物 脂肪生成 癌细胞 癌症研究 药理学 生物信息学 细胞生物学 生物化学 脂肪组织 遗传学 磷脂 蛋白激酶C
作者
Elizabeth G. Slane,Samantha J. Tambrini,Brian S. Cummings
出处
期刊:Biochemical Pharmacology [Elsevier BV]
卷期号:222: 116106-116106 被引量:3
标识
DOI:10.1016/j.bcp.2024.116106
摘要

Lipins are phosphatidic acid phosphatases (PAP) that catalyze the conversion of phosphatidic acid (PA) to diacylglycerol (DAG). Three lipin isoforms have been identified: lipin-1, -2 and -3. In addition to their PAP activity, lipin-1 and -2 act as transcriptional coactivators and corepressors. Lipins have been intensely studied for their role in regulation of lipid metabolism and adipogenesis; however, lipins are hypothesized to mediate several pathologies, such as those involving metabolic diseases, neuropathy and even cognitive impairment. Recently, an emerging role for lipins have been proposed in cancer. The study of lipins in cancer has been hampered by lack of inhibitors that have selectivity for lipins, that differentiate between lipin family members, or that are suitable for in vivo studies. Such inhibitors have the potential to be extremely useful as both molecular tools and therapeutics. This review describes the expression and function of lipins in various tissues and their roles in several diseases, but with an emphasis on their possible role in cancer The mechanisms by which lipins mediate cancer cell growth are discussed and the potential usefulness of selective lipin inhibitors is hypothesized. Finally, recent studies reporting the crystallization of lipin-1 are discussed to facilitate rational design of novel lipin inhibitors.
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