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磷脂酶D作为一种新治疗靶点的潜力。

The potential for phospholipase D as a new therapeutic target.

作者信息

Huang Ping, Frohman Michael A

机构信息

University Medical Center at Stony Brook, Department of Pharmacology and the Center for Developmental Genetics, Stony Brook, NY 11794-5140, USA.

出版信息

Expert Opin Ther Targets. 2007 May;11(5):707-16. doi: 10.1517/14728222.11.5.707.

Abstract

Mammalian phospholipase D (PLD), a signal transduction-activated enzyme, hydrolyzes phosphatidylcholine to generate the lipid second messenger phosphatidic acid (PA) and choline. Genetic and pharmacological methods have implicated PLD and its product PA in a wide variety of cellular processes including vesicle trafficking, receptor signaling, cell proliferation and survival. Dysregulation of these cell biologic processes occurs in a diverse range of illnesses including cancer. This review summarizes PLD regulation and function and highlights its potential as a therapeutic target in disease settings.

摘要

哺乳动物磷脂酶D(PLD)是一种信号转导激活酶,它水解磷脂酰胆碱生成脂质第二信使磷脂酸(PA)和胆碱。遗传学和药理学方法已表明PLD及其产物PA参与了包括囊泡运输、受体信号传导、细胞增殖和存活在内的多种细胞过程。这些细胞生物学过程的失调发生在包括癌症在内的多种疾病中。本综述总结了PLD的调节和功能,并强调了其作为疾病治疗靶点的潜力。

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