Literature DB >> 14732197

The ubiquitin-proteasome system in cardiovascular diseases-a hypothesis extended.

Joerg Herrmann1, Aaron Ciechanover, Lilach O Lerman, Amir Lerman.   

Abstract

During recent years, the ubiquitin-proteasome system has become known as the major pathway of non-lysosomal degradation of intracellular proteins, involving two sequential steps. In the first step, multiple moieties of ubiquitin are covalently bound to target proteins to be recognized and degraded by the multi-enzymatic proteasome complex in the second step. In addition to the elimination of damaged and unneeded proteins, this system fulfills an important function in the regulation of cellular mediators in various biological pathways. Foremost, these biological pathways include inflammation, cell proliferation, and apoptosis, all of which constitute important characteristics of atherosclerosis. Indeed, recent experimental evidence supports a potential involvement of the ubiquitin-proteasome system in the initiation, progression, and complication stage of atherogenesis. This review summarizes recent findings regarding the ubiquitin-proteasome system in cardiovascular diseases and discusses the potential use of proteasome inhibitors in cardiovascular therapy.

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Year:  2004        PMID: 14732197     DOI: 10.1016/j.cardiores.2003.09.033

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  59 in total

Review 1.  The ubiquitin-proteasome system and cardiovascular disease.

Authors:  Saul R Powell; Joerg Herrmann; Amir Lerman; Cam Patterson; Xuejun Wang
Journal:  Prog Mol Biol Transl Sci       Date:  2012       Impact factor: 3.622

Review 2.  Seven-transmembrane receptors and ubiquitination.

Authors:  Sudha K Shenoy
Journal:  Circ Res       Date:  2007-04-27       Impact factor: 17.367

3.  Clinical significance of single nucleotide polymorphisms in PCSK9.

Authors:  Ali J Marian
Journal:  Curr Atheroscler Rep       Date:  2007-09       Impact factor: 5.113

Review 4.  On to the road to degradation: atherosclerosis and the proteasome.

Authors:  Joerg Herrmann; Lilach O Lerman; Amir Lerman
Journal:  Cardiovasc Res       Date:  2009-10-08       Impact factor: 10.787

5.  Ubiquitin-activating enzyme E1 inhibitor PYR41 attenuates angiotensin II-induced activation of dendritic cells via the IκBa/NF-κB and MKP1/ERK/STAT1 pathways.

Authors:  Chen Chen; Yan Meng; Lei Wang; Hong-Xia Wang; Cui Tian; Guo-Dong Pang; Hui-Hua Li; Jie Du
Journal:  Immunology       Date:  2014-06       Impact factor: 7.397

Review 6.  Taking pressure off the heart: the ins and outs of atrophic remodelling.

Authors:  Kedryn K Baskin; Heinrich Taegtmeyer
Journal:  Cardiovasc Res       Date:  2011-02-25       Impact factor: 10.787

7.  Adhesion-dependent Skp2 transcription requires selenocysteine tRNA gene transcription-activating factor (STAF).

Authors:  Ivette Hernández-Negrete; Graciela B Sala-Newby; Andras Perl; Gary R Kunkel; Andrew C Newby; Mark Bond
Journal:  Biochem J       Date:  2011-05-15       Impact factor: 3.857

8.  Proteasome Inhibitor Reduces Astrocytic iNOS Expression and Functional Deficit after Experimental Intracerebral Hemorrhage in Rats.

Authors:  Fahmi M Al-Senani; Xiurong Zhao; James C Grotta; Ali Shirzadi; Roger Strong; Jaroslaw Aronowski
Journal:  Transl Stroke Res       Date:  2011-10-19       Impact factor: 6.829

Review 9.  Breaking down protein degradation mechanisms in cardiac muscle.

Authors:  Robert C Lyon; Stephan Lange; Farah Sheikh
Journal:  Trends Mol Med       Date:  2013-02-27       Impact factor: 11.951

Review 10.  Cardiac toxicity: old and new issues in anti-cancer drugs.

Authors:  M Sereno; A Brunello; A Chiappori; J Barriuso; E Casado; C Belda; J de Castro; J Feliu; M González-Barón
Journal:  Clin Transl Oncol       Date:  2008-01       Impact factor: 3.405

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