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The flip side of doxorubicin: Inflammatory and tumor promoting cytokines

Cardiac toxicity is a major dose-limiting factor for the anthracycline drug doxorubicin. The reasons why doxorubicin causes heart damage are not fully understood, and the manuscript by Wong et al. postulates that inflammatory cytokines released from macrophages or other cell types may play a signifi...

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Detalles Bibliográficos
Autor principal: Dent, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909543/
https://www.ncbi.nlm.nih.gov/pubmed/23974349
http://dx.doi.org/10.4161/cbt.26125
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author Dent, Paul
author_facet Dent, Paul
author_sort Dent, Paul
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description Cardiac toxicity is a major dose-limiting factor for the anthracycline drug doxorubicin. The reasons why doxorubicin causes heart damage are not fully understood, and the manuscript by Wong et al. postulates that inflammatory cytokines released from macrophages or other cell types may play a significant role in the damage process in response to doxorubicin and possibly other chemotherapeutic agents.(1) Expression of many cytokines requires activation of both the p38 MAPK and JNK pathways and, additionally, doxorubicin toxicity can be blocked by combined inhibition of both pathways.(2)(,)(3) The MAP3K responsible for doxorubicin-induced p38 MAPK and JNK activation in keratinocytes was previously shown by these authors to be ZAK.(4) ZAK is of note because it can be targeted by FDA approved agents such as nilotinib and sorafenib.(4)(-)(7)
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spelling pubmed-39095432014-02-10 The flip side of doxorubicin: Inflammatory and tumor promoting cytokines Dent, Paul Cancer Biol Ther Commentary Cardiac toxicity is a major dose-limiting factor for the anthracycline drug doxorubicin. The reasons why doxorubicin causes heart damage are not fully understood, and the manuscript by Wong et al. postulates that inflammatory cytokines released from macrophages or other cell types may play a significant role in the damage process in response to doxorubicin and possibly other chemotherapeutic agents.(1) Expression of many cytokines requires activation of both the p38 MAPK and JNK pathways and, additionally, doxorubicin toxicity can be blocked by combined inhibition of both pathways.(2)(,)(3) The MAP3K responsible for doxorubicin-induced p38 MAPK and JNK activation in keratinocytes was previously shown by these authors to be ZAK.(4) ZAK is of note because it can be targeted by FDA approved agents such as nilotinib and sorafenib.(4)(-)(7) Landes Bioscience 2013-09-01 2013-08-12 /pmc/articles/PMC3909543/ /pubmed/23974349 http://dx.doi.org/10.4161/cbt.26125 Text en Copyright © 2013 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
Dent, Paul
The flip side of doxorubicin: Inflammatory and tumor promoting cytokines
title The flip side of doxorubicin: Inflammatory and tumor promoting cytokines
title_full The flip side of doxorubicin: Inflammatory and tumor promoting cytokines
title_fullStr The flip side of doxorubicin: Inflammatory and tumor promoting cytokines
title_full_unstemmed The flip side of doxorubicin: Inflammatory and tumor promoting cytokines
title_short The flip side of doxorubicin: Inflammatory and tumor promoting cytokines
title_sort flip side of doxorubicin: inflammatory and tumor promoting cytokines
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909543/
https://www.ncbi.nlm.nih.gov/pubmed/23974349
http://dx.doi.org/10.4161/cbt.26125
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