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Crosstalk between p53 and TGF-β Signalling
Wild-type p53 and TGF-β are key tumour suppressors which regulate an array of cellular responses. TGF-β signals in part via the Smad signal transduction pathway. Wild-type p53 and Smads physically interact and coordinately induce transcription of a number of key tumour suppressive genes. Conversely...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3321553/ https://www.ncbi.nlm.nih.gov/pubmed/22545213 http://dx.doi.org/10.1155/2012/294097 |
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author | Elston, Rebecca Inman, Gareth J. |
author_facet | Elston, Rebecca Inman, Gareth J. |
author_sort | Elston, Rebecca |
collection | PubMed |
description | Wild-type p53 and TGF-β are key tumour suppressors which regulate an array of cellular responses. TGF-β signals in part via the Smad signal transduction pathway. Wild-type p53 and Smads physically interact and coordinately induce transcription of a number of key tumour suppressive genes. Conversely mutant p53 generally subverts tumour suppressive TGF-β responses, diminishing transcriptional activation of key TGF-β target genes. Mutant p53 can also interact with Smads and this enables complex formation with the p53 family member p63 and blocks p63-mediated activation of metastasis suppressing genes to promote tumour progression. p53 and Smad function may also overlap during miRNA biogenesis as they can interact with the same components of the Drosha miRNA processing complex to promote maturation of specific subsets of miRNAs. This paper investigates the crosstalk between p53 and TGF-β signalling and the potential roles this plays in cancer biology. |
format | Online Article Text |
id | pubmed-3321553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33215532012-04-27 Crosstalk between p53 and TGF-β Signalling Elston, Rebecca Inman, Gareth J. J Signal Transduct Review Article Wild-type p53 and TGF-β are key tumour suppressors which regulate an array of cellular responses. TGF-β signals in part via the Smad signal transduction pathway. Wild-type p53 and Smads physically interact and coordinately induce transcription of a number of key tumour suppressive genes. Conversely mutant p53 generally subverts tumour suppressive TGF-β responses, diminishing transcriptional activation of key TGF-β target genes. Mutant p53 can also interact with Smads and this enables complex formation with the p53 family member p63 and blocks p63-mediated activation of metastasis suppressing genes to promote tumour progression. p53 and Smad function may also overlap during miRNA biogenesis as they can interact with the same components of the Drosha miRNA processing complex to promote maturation of specific subsets of miRNAs. This paper investigates the crosstalk between p53 and TGF-β signalling and the potential roles this plays in cancer biology. Hindawi Publishing Corporation 2012 2012-03-28 /pmc/articles/PMC3321553/ /pubmed/22545213 http://dx.doi.org/10.1155/2012/294097 Text en Copyright © 2012 R. Elston and G. J. Inman. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Elston, Rebecca Inman, Gareth J. Crosstalk between p53 and TGF-β Signalling |
title | Crosstalk between p53 and TGF-β Signalling |
title_full | Crosstalk between p53 and TGF-β Signalling |
title_fullStr | Crosstalk between p53 and TGF-β Signalling |
title_full_unstemmed | Crosstalk between p53 and TGF-β Signalling |
title_short | Crosstalk between p53 and TGF-β Signalling |
title_sort | crosstalk between p53 and tgf-β signalling |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3321553/ https://www.ncbi.nlm.nih.gov/pubmed/22545213 http://dx.doi.org/10.1155/2012/294097 |
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