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STAT5 acetylation: Mechanisms and consequences for immunological control and leukemogenesis
The cytokine-inducible transcription factors signal transducer and activator of transcription 5A and 5B (STAT5A and STAT5B) are important for the proper development of multicellular eukaryotes. Disturbed signaling cascades evoking uncontrolled expression of STAT5 target genes are associated with can...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876427/ https://www.ncbi.nlm.nih.gov/pubmed/24416653 http://dx.doi.org/10.4161/jkst.26102 |
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author | Kosan, Christian Ginter, Torsten Heinzel, Thorsten Krämer, Oliver H |
author_facet | Kosan, Christian Ginter, Torsten Heinzel, Thorsten Krämer, Oliver H |
author_sort | Kosan, Christian |
collection | PubMed |
description | The cytokine-inducible transcription factors signal transducer and activator of transcription 5A and 5B (STAT5A and STAT5B) are important for the proper development of multicellular eukaryotes. Disturbed signaling cascades evoking uncontrolled expression of STAT5 target genes are associated with cancer and immunological failure. Here, we summarize how STAT5 acetylation is integrated into posttranslational modification networks within cells. Moreover, we focus on how inhibitors of deacetylases and tyrosine kinases can correct leukemogenic signaling nodes involving STAT5. Such small molecules can be exploited in the fight against neoplastic diseases and immunological disorders. |
format | Online Article Text |
id | pubmed-3876427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-38764272014-01-10 STAT5 acetylation: Mechanisms and consequences for immunological control and leukemogenesis Kosan, Christian Ginter, Torsten Heinzel, Thorsten Krämer, Oliver H JAKSTAT Review The cytokine-inducible transcription factors signal transducer and activator of transcription 5A and 5B (STAT5A and STAT5B) are important for the proper development of multicellular eukaryotes. Disturbed signaling cascades evoking uncontrolled expression of STAT5 target genes are associated with cancer and immunological failure. Here, we summarize how STAT5 acetylation is integrated into posttranslational modification networks within cells. Moreover, we focus on how inhibitors of deacetylases and tyrosine kinases can correct leukemogenic signaling nodes involving STAT5. Such small molecules can be exploited in the fight against neoplastic diseases and immunological disorders. Landes Bioscience 2013-10-01 2013-08-19 /pmc/articles/PMC3876427/ /pubmed/24416653 http://dx.doi.org/10.4161/jkst.26102 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 Kosan, Christian Ginter, Torsten Heinzel, Thorsten Krämer, Oliver H STAT5 acetylation: Mechanisms and consequences for immunological control and leukemogenesis |
title | STAT5 acetylation: Mechanisms and consequences for immunological control and leukemogenesis |
title_full | STAT5 acetylation: Mechanisms and consequences for immunological control and leukemogenesis |
title_fullStr | STAT5 acetylation: Mechanisms and consequences for immunological control and leukemogenesis |
title_full_unstemmed | STAT5 acetylation: Mechanisms and consequences for immunological control and leukemogenesis |
title_short | STAT5 acetylation: Mechanisms and consequences for immunological control and leukemogenesis |
title_sort | stat5 acetylation: mechanisms and consequences for immunological control and leukemogenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876427/ https://www.ncbi.nlm.nih.gov/pubmed/24416653 http://dx.doi.org/10.4161/jkst.26102 |
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