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IL-6-STAT3 signaling and premature senescence

Cytokines play several roles in developing and/or reinforcing premature cellular senescence of young cells. One such cytokine, interleukin-6 (IL-6), regulates senescence in some systems in addition to its known functions of immune regulation and promotion of tumorigenesis. In this review, we describ...

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Autores principales: Kojima, Hirotada, Inoue, Toshiaki, Kunimoto, Hiroyuki, Nakajima, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876432/
https://www.ncbi.nlm.nih.gov/pubmed/24416650
http://dx.doi.org/10.4161/jkst.25763
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author Kojima, Hirotada
Inoue, Toshiaki
Kunimoto, Hiroyuki
Nakajima, Koichi
author_facet Kojima, Hirotada
Inoue, Toshiaki
Kunimoto, Hiroyuki
Nakajima, Koichi
author_sort Kojima, Hirotada
collection PubMed
description Cytokines play several roles in developing and/or reinforcing premature cellular senescence of young cells. One such cytokine, interleukin-6 (IL-6), regulates senescence in some systems in addition to its known functions of immune regulation and promotion of tumorigenesis. In this review, we describe recent advances in studies on the roles of IL-6 and its downstream signal transducer and activator of transcription 3 (STAT3) in regulating premature cellular senescence. IL-6/sIL-6Rα stimulation forms a senescence-inducing circuit involving the STAT3-insulin-like growth factor-binding protein 5 (IGFBP5) as a key axis triggering and reinforcing component in human fibroblasts. We describe how cytokines regulate the process of senescence by activating STAT3 in one system and anti-senescence or tumorigenesis in other systems. The roles of other STAT members in premature senescence also will be discussed to show the multiple mechanisms leading to cytokine-induced senescence.
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spelling pubmed-38764322014-01-10 IL-6-STAT3 signaling and premature senescence Kojima, Hirotada Inoue, Toshiaki Kunimoto, Hiroyuki Nakajima, Koichi JAKSTAT Review Cytokines play several roles in developing and/or reinforcing premature cellular senescence of young cells. One such cytokine, interleukin-6 (IL-6), regulates senescence in some systems in addition to its known functions of immune regulation and promotion of tumorigenesis. In this review, we describe recent advances in studies on the roles of IL-6 and its downstream signal transducer and activator of transcription 3 (STAT3) in regulating premature cellular senescence. IL-6/sIL-6Rα stimulation forms a senescence-inducing circuit involving the STAT3-insulin-like growth factor-binding protein 5 (IGFBP5) as a key axis triggering and reinforcing component in human fibroblasts. We describe how cytokines regulate the process of senescence by activating STAT3 in one system and anti-senescence or tumorigenesis in other systems. The roles of other STAT members in premature senescence also will be discussed to show the multiple mechanisms leading to cytokine-induced senescence. Landes Bioscience 2013-10-01 2013-07-22 /pmc/articles/PMC3876432/ /pubmed/24416650 http://dx.doi.org/10.4161/jkst.25763 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 Review
Kojima, Hirotada
Inoue, Toshiaki
Kunimoto, Hiroyuki
Nakajima, Koichi
IL-6-STAT3 signaling and premature senescence
title IL-6-STAT3 signaling and premature senescence
title_full IL-6-STAT3 signaling and premature senescence
title_fullStr IL-6-STAT3 signaling and premature senescence
title_full_unstemmed IL-6-STAT3 signaling and premature senescence
title_short IL-6-STAT3 signaling and premature senescence
title_sort il-6-stat3 signaling and premature senescence
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876432/
https://www.ncbi.nlm.nih.gov/pubmed/24416650
http://dx.doi.org/10.4161/jkst.25763
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