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Necroptosis: STAT3 kills?

TNF-induced necroptosis is caused by the activation of RIPK1 and the subsequent production of reactive oxygen species in the mitochondria, although the intermittent molecules of the signaling pathway responsible for this ROS-mediated type of programmed necrosis have not yet been identified. A recent...

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Detalles Bibliográficos
Autores principales: Georgiadis, Vassilis, Knight, Richard A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670246/
https://www.ncbi.nlm.nih.gov/pubmed/24058772
http://dx.doi.org/10.4161/jkst.20968
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author Georgiadis, Vassilis
Knight, Richard A.
author_facet Georgiadis, Vassilis
Knight, Richard A.
author_sort Georgiadis, Vassilis
collection PubMed
description TNF-induced necroptosis is caused by the activation of RIPK1 and the subsequent production of reactive oxygen species in the mitochondria, although the intermittent molecules of the signaling pathway responsible for this ROS-mediated type of programmed necrosis have not yet been identified. A recent article by Shulga and Pastorino in the Journal of Cell Science identifies RIPK1 as the mediator of STAT3 Ser727 phosphorylation, which leads to the translocation of the latter into the mitochondria via its interaction with GRIM-19, a member of the mitochondrial complex I. Here we discuss how the findings of the Shulga and Pastorino study shed light onto the involvement of STAT3 in necroptosis.
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spelling pubmed-36702462013-09-19 Necroptosis: STAT3 kills? Georgiadis, Vassilis Knight, Richard A. JAKSTAT Commentary TNF-induced necroptosis is caused by the activation of RIPK1 and the subsequent production of reactive oxygen species in the mitochondria, although the intermittent molecules of the signaling pathway responsible for this ROS-mediated type of programmed necrosis have not yet been identified. A recent article by Shulga and Pastorino in the Journal of Cell Science identifies RIPK1 as the mediator of STAT3 Ser727 phosphorylation, which leads to the translocation of the latter into the mitochondria via its interaction with GRIM-19, a member of the mitochondrial complex I. Here we discuss how the findings of the Shulga and Pastorino study shed light onto the involvement of STAT3 in necroptosis. Landes Bioscience 2012-07-01 2012-07-01 /pmc/articles/PMC3670246/ /pubmed/24058772 http://dx.doi.org/10.4161/jkst.20968 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
Georgiadis, Vassilis
Knight, Richard A.
Necroptosis: STAT3 kills?
title Necroptosis: STAT3 kills?
title_full Necroptosis: STAT3 kills?
title_fullStr Necroptosis: STAT3 kills?
title_full_unstemmed Necroptosis: STAT3 kills?
title_short Necroptosis: STAT3 kills?
title_sort necroptosis: stat3 kills?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670246/
https://www.ncbi.nlm.nih.gov/pubmed/24058772
http://dx.doi.org/10.4161/jkst.20968
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