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Decoding RAS isoform and codon-specific signalling
RAS proteins are key signalling hubs that are oncogenically mutated in 30% of all cancer cases. Three genes encode almost identical isoforms that are ubiquitously expressed, but are not functionally redundant. The network responses associated with each isoform and individual oncogenic mutations rema...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961500/ https://www.ncbi.nlm.nih.gov/pubmed/25109951 http://dx.doi.org/10.1042/BST20140057 |
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author | Newlaczyl, Anna U. Hood, Fiona E. Coulson, Judy M. Prior, Ian A. |
author_facet | Newlaczyl, Anna U. Hood, Fiona E. Coulson, Judy M. Prior, Ian A. |
author_sort | Newlaczyl, Anna U. |
collection | PubMed |
description | RAS proteins are key signalling hubs that are oncogenically mutated in 30% of all cancer cases. Three genes encode almost identical isoforms that are ubiquitously expressed, but are not functionally redundant. The network responses associated with each isoform and individual oncogenic mutations remain to be fully characterized. In the present article, we review recent data defining the differences between the RAS isoforms and their most commonly mutated codons and discuss the underlying mechanisms. |
format | Online Article Text |
id | pubmed-4961500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49615002016-07-27 Decoding RAS isoform and codon-specific signalling Newlaczyl, Anna U. Hood, Fiona E. Coulson, Judy M. Prior, Ian A. Biochem Soc Trans Biochemical Society Focused Meetings RAS proteins are key signalling hubs that are oncogenically mutated in 30% of all cancer cases. Three genes encode almost identical isoforms that are ubiquitously expressed, but are not functionally redundant. The network responses associated with each isoform and individual oncogenic mutations remain to be fully characterized. In the present article, we review recent data defining the differences between the RAS isoforms and their most commonly mutated codons and discuss the underlying mechanisms. Portland Press Ltd. 2014-08-11 2014-08-01 /pmc/articles/PMC4961500/ /pubmed/25109951 http://dx.doi.org/10.1042/BST20140057 Text en © 2014 The Author(s) http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biochemical Society Focused Meetings Newlaczyl, Anna U. Hood, Fiona E. Coulson, Judy M. Prior, Ian A. Decoding RAS isoform and codon-specific signalling |
title | Decoding RAS isoform and codon-specific signalling |
title_full | Decoding RAS isoform and codon-specific signalling |
title_fullStr | Decoding RAS isoform and codon-specific signalling |
title_full_unstemmed | Decoding RAS isoform and codon-specific signalling |
title_short | Decoding RAS isoform and codon-specific signalling |
title_sort | decoding ras isoform and codon-specific signalling |
topic | Biochemical Society Focused Meetings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961500/ https://www.ncbi.nlm.nih.gov/pubmed/25109951 http://dx.doi.org/10.1042/BST20140057 |
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