Blocking the PI3K/PKB pathway in tumor cells.

Frédéric Stauffer, Philipp Holzer, Carlos García-Echeverría
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引用次数: 38

Abstract

A substantial number of experimental and epidemiological studies support an important role for the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (PKB) pathway in the biology of human cancers. Components of this signaling cascade have been found to be deregulated in a wide range of solid tumors and hematologic malignancies, and extensive anti-cancer therapeutic programs are now devoted to the identification of agents that specifically block this molecular pathway. This article focuses on the current knowledge of the alterations of the PI3K/PKB pathway in cancer cells and ongoing drug discovery efforts to therapeutically target it. Particular emphasis is placed on medicinal chemistry activities to identify and develop compounds able to modulate the kinase activity of its main molecular components.

阻断肿瘤细胞中PI3K/PKB通路。
大量的实验和流行病学研究支持磷脂酰肌醇3-激酶(PI3K)/蛋白激酶B (PKB)通路在人类癌症生物学中的重要作用。这一信号级联的组成部分已被发现在广泛的实体肿瘤和血液系统恶性肿瘤中被解除调控,现在广泛的抗癌治疗项目致力于识别特异性阻断这一分子途径的药物。本文主要关注癌细胞中PI3K/PKB通路的改变和正在进行的药物发现工作,以治疗它。特别强调的是药物化学活动,以确定和开发能够调节其主要分子成分的激酶活性的化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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