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The interplay between inhibition of JAK2 and HSP90

A recent article by Weigert et al. published in The Journal of Experimental Medicine described the in vitro generation of synthetic mutations in Janus kinase 2 (JAK 2) that decreased the potency of JAK2 (or JAK1/JAK2) inhibitors in artificial systems. The authors found that heat shock protein 90 (HS...

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Detalles Bibliográficos
Autores principales: Fridman, Jordan S., Sarlis, Nicholas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670297/
https://www.ncbi.nlm.nih.gov/pubmed/24058754
http://dx.doi.org/10.4161/jkst.20293
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author Fridman, Jordan S.
Sarlis, Nicholas J.
author_facet Fridman, Jordan S.
Sarlis, Nicholas J.
author_sort Fridman, Jordan S.
collection PubMed
description A recent article by Weigert et al. published in The Journal of Experimental Medicine described the in vitro generation of synthetic mutations in Janus kinase 2 (JAK 2) that decreased the potency of JAK2 (or JAK1/JAK2) inhibitors in artificial systems. The authors found that heat shock protein 90 (HSP90) inhibitors circumvented the potency shift and suggested that HSP90 inhibition may abrogate JAK inhibitor resistance in these experimental systems. However, the clinical relevance of these laboratory-generated JAK2 mutations, which have not been identified to-date in patients treated with JAK inhibitors, and the therapeutic potential of HSP90 inhibitors in diseases involving aberrant JAK-STAT signaling remain to be determined.
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spelling pubmed-36702972013-09-19 The interplay between inhibition of JAK2 and HSP90 Fridman, Jordan S. Sarlis, Nicholas J. JAKSTAT Commentary A recent article by Weigert et al. published in The Journal of Experimental Medicine described the in vitro generation of synthetic mutations in Janus kinase 2 (JAK 2) that decreased the potency of JAK2 (or JAK1/JAK2) inhibitors in artificial systems. The authors found that heat shock protein 90 (HSP90) inhibitors circumvented the potency shift and suggested that HSP90 inhibition may abrogate JAK inhibitor resistance in these experimental systems. However, the clinical relevance of these laboratory-generated JAK2 mutations, which have not been identified to-date in patients treated with JAK inhibitors, and the therapeutic potential of HSP90 inhibitors in diseases involving aberrant JAK-STAT signaling remain to be determined. Landes Bioscience 2012-04-01 /pmc/articles/PMC3670297/ /pubmed/24058754 http://dx.doi.org/10.4161/jkst.20293 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Commentary
Fridman, Jordan S.
Sarlis, Nicholas J.
The interplay between inhibition of JAK2 and HSP90
title The interplay between inhibition of JAK2 and HSP90
title_full The interplay between inhibition of JAK2 and HSP90
title_fullStr The interplay between inhibition of JAK2 and HSP90
title_full_unstemmed The interplay between inhibition of JAK2 and HSP90
title_short The interplay between inhibition of JAK2 and HSP90
title_sort interplay between inhibition of jak2 and hsp90
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670297/
https://www.ncbi.nlm.nih.gov/pubmed/24058754
http://dx.doi.org/10.4161/jkst.20293
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