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  5. The Role of MAPK in Drug-Induced Kidney Injury
 
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The Role of MAPK in Drug-Induced Kidney Injury

Author(s)
Cassidy, Hilary  
Radford, Robert  
Slyne, Jennifer  
O'Connell, Séin  
Slattery, Craig  
Ryan, Michael P.  
McMorrow, Tara  
Uri
http://hdl.handle.net/10197/3747
Date Issued
2012
Date Available
2012-08-17T15:10:55Z
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.
Sponsorship
European Research Council
Type of Material
Journal Article
Publisher
Hindawi Publishers
Journal
Journal of Signal Transduction
Volume
2012
Copyright (Published Version)
2012 Hilary Cassidy et al.
Subjects

Kidney Disease

MapK

Subject – LCSH
Mitogen-activated protein kinases
Drugs--Side effects
Kidneys--Diseases
DOI
10.1155/2012/463617
Language
English
Status of Item
Peer reviewed
This item is made available under a Creative Commons License
https://creativecommons.org/licenses/by-nc-sa/1.0/
File(s)
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JST MApK review Cassidy 12 463617[1].pdf

Size

13.77 MB

Format

Adobe PDF

Checksum (MD5)

6ba069d539b7f89ae5186264cf6bd425

Owning collection
Conway Institute Research Collection
Mapped collections
Biomolecular and Biomedical Science Research Collection

Item descriptive metadata is released under a CC-0 (public domain) license: https://creativecommons.org/public-domain/cc0/.
All other content is subject to copyright.

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