Hsp27 (HspB1) and αB-crystallin (HspB5) as therapeutic targets

被引:293
作者
Arrigo, Andr-Patrick
Simon, Stphanie
Gibert, Benjamin
Kretz-Remy, Carole
Nivon, Mathieu
Czekalla, Anna
Guillet, Dominique
Moulin, Maryline
Diaz-Latoud, Chantal
Vicart, Patrick
机构
[1] Univ Lyon 1, Ctr Genet Mol & Cellulaire, CNRS, UMR5534,Lab Stress Chaperons & Mort Cellulaire, F-69622 Villeurbanne, France
[2] Univ Paris 07, UFR Biochim, Paris, France
关键词
Hsp27; alpha B-crystallin; neurodegenerative diseases; myopathies; cancers;
D O I
10.1016/j.febslet.2007.04.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Hsp27 and alpha B-crystallin are molecular chaperones that are constitutively expressed in several mammalian cells, particularly in pathological conditions. These proteins share functions as diverse as protection against toxicity mediated by aberrantly folded proteins or oxidative-inflammation conditions. In addition, these proteins share anti-apoptotic properties and are tumorigenic when expressed in cancer cells. This review summarizes the current knowledge about Hsp27 and alpha B-crystallin and the implications, either positive or deleterious, of these proteins in pathologies such as neurodegenerative diseases, myopathies, asthma, cataracts and cancers. Approaches towards therapeutic strategies aimed at modulating the expression and/or the activities of Hsp27 and aB-crystallin are presented. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3665 / 3674
页数:10
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