The role of MAPK in drug-induced kidney injury.

Journal of signal transduction Pub Date : 2012-01-01 Epub Date: 2012-03-12 DOI:10.1155/2012/463617
Hilary Cassidy, Robert Radford, Jennifer Slyne, Sein O'Connell, Craig Slattery, Michael P Ryan, Tara McMorrow
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引用次数: 47

Abstract

This paper focuses on the role that mitogen-activated protein kinases (MAPKs) play in drug-induced kidney injury. The MAPKs, of which there are four major classes (ERK, p38, JNK, and ERK5/BMK), are signalling cascades which have been found to be broadly conserved across a wide variety of organisms. MAPKs allow effective transmission of information from the cell surface to the cytosolic or nuclear compartments. Cross talk between the MAPKs themselves and with other signalling pathways allows the cell to modulate responses to a wide variety of external stimuli. The MAPKs have been shown to play key roles in both mediating and ameliorating cellular responses to stress including xenobiotic-induced toxicity. Therefore, this paper will discuss the specific role of the MAPKs in the kidney in response to injury by a variety of xenobiotics and the potential for therapeutic intervention at the level of MAPK signalling across different types of kidney disease.

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MAPK在药物性肾损伤中的作用。
本文主要探讨丝裂原活化蛋白激酶(MAPKs)在药物性肾损伤中的作用。mapk,其中有四大类(ERK, p38, JNK和ERK5/BMK),是信号级联,已被发现在多种生物中广泛保守。MAPKs允许信息有效地从细胞表面传递到细胞质或核室。mapk本身和其他信号通路之间的串扰允许细胞调节对各种外部刺激的反应。MAPKs已被证明在介导和改善细胞对包括外源诱导的毒性在内的应激反应中发挥关键作用。因此,本文将讨论MAPK在肾脏对各种外源药物损伤的反应中的具体作用,以及在不同类型肾脏疾病的MAPK信号水平上进行治疗干预的潜力。
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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