Developing small molecules to inhibit kinases unkind to the heart: p38 MAPK as a case in point

Michael S. Marber , Jeffery D. Molkentin , Thomas Force
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引用次数: 29

Abstract

Over the past 40 years targeting G-protein-coupled receptors and their ligands has had a major impact on the treatment of cardiovascular disease. However, the past decade has seen little progress and focus has shifted, particularly in the field of cancer biology, to downstream kinases. This review focuses on the kinases within the heart that become active during myocardial infarction and heart failure and contribute to cardiac dysfunction, with a special emphasis on p38 mitogen-activated protein kinase (MAPK).

开发小分子来抑制对心脏不利的激酶:p38 MAPK就是一个很好的例子
在过去的40年里,靶向g蛋白偶联受体及其配体对心血管疾病的治疗产生了重大影响。然而,在过去的十年中,进展甚微,重点已经转移到下游激酶,特别是在癌症生物学领域。本文综述了心肌梗死和心力衰竭期间心脏内活跃并导致心功能障碍的激酶,特别强调了p38丝裂原活化蛋白激酶(MAPK)。
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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