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S6K2: The Neglected S6 Kinase Family Member
S6 kinase 2 (S6K2) is a member of the AGC kinases super-family. Its closest homolog, S6K1, has been extensively studied along the years. However, due to the belief in the community that the high degree of identity between these two isoforms would translate in essentially identical biological functio...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721059/ https://www.ncbi.nlm.nih.gov/pubmed/23898460 http://dx.doi.org/10.3389/fonc.2013.00191 |
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author | Pardo, Olivier E. Seckl, Michael J. |
author_facet | Pardo, Olivier E. Seckl, Michael J. |
author_sort | Pardo, Olivier E. |
collection | PubMed |
description | S6 kinase 2 (S6K2) is a member of the AGC kinases super-family. Its closest homolog, S6K1, has been extensively studied along the years. However, due to the belief in the community that the high degree of identity between these two isoforms would translate in essentially identical biological functions, S6K2 has been largely neglected. Nevertheless, recent research has clearly highlighted that these two proteins significantly differ in their roles in vitro as well as in vivo. These findings are significant to our understanding of S6 kinase signaling and the development of therapeutic strategies for several diseases including cancer. Here, we will focus on S6K2 and review the protein–protein interactions and specific substrates that determine the selective functions of this kinase. |
format | Online Article Text |
id | pubmed-3721059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37210592013-07-29 S6K2: The Neglected S6 Kinase Family Member Pardo, Olivier E. Seckl, Michael J. Front Oncol Oncology S6 kinase 2 (S6K2) is a member of the AGC kinases super-family. Its closest homolog, S6K1, has been extensively studied along the years. However, due to the belief in the community that the high degree of identity between these two isoforms would translate in essentially identical biological functions, S6K2 has been largely neglected. Nevertheless, recent research has clearly highlighted that these two proteins significantly differ in their roles in vitro as well as in vivo. These findings are significant to our understanding of S6 kinase signaling and the development of therapeutic strategies for several diseases including cancer. Here, we will focus on S6K2 and review the protein–protein interactions and specific substrates that determine the selective functions of this kinase. Frontiers Media S.A. 2013-07-24 /pmc/articles/PMC3721059/ /pubmed/23898460 http://dx.doi.org/10.3389/fonc.2013.00191 Text en Copyright © 2013 Pardo and Seckl. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Oncology Pardo, Olivier E. Seckl, Michael J. S6K2: The Neglected S6 Kinase Family Member |
title | S6K2: The Neglected S6 Kinase Family Member |
title_full | S6K2: The Neglected S6 Kinase Family Member |
title_fullStr | S6K2: The Neglected S6 Kinase Family Member |
title_full_unstemmed | S6K2: The Neglected S6 Kinase Family Member |
title_short | S6K2: The Neglected S6 Kinase Family Member |
title_sort | s6k2: the neglected s6 kinase family member |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721059/ https://www.ncbi.nlm.nih.gov/pubmed/23898460 http://dx.doi.org/10.3389/fonc.2013.00191 |
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