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Regulation of the interferon-gamma (IFN-γ) pathway by p63 and Δ133p53 isoform in different breast cancer subtypes

The TP53 family consists of three sets of transcription factor genes, TP53, TP63 and TP73, each of which expresses multiple RNA variants and protein isoforms. Of these, TP53 is mutated in 25-30% of breast cancers. How TP53 mutations affect the interaction of TP53 family members and their isoforms in...

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Autores principales: Mehta, Sunali Y., Morten, Brianna C., Antony, Jisha, Henderson, Luke, Lasham, Annette, Campbell, Hamish, Cunliffe, Heather, Horsfield, Julia A., Reddel, Roger R., Avery-Kiejda, Kelly A., Print, Cristin G., Braithwaite, Antony W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044385/
https://www.ncbi.nlm.nih.gov/pubmed/30018742
http://dx.doi.org/10.18632/oncotarget.25635
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author Mehta, Sunali Y.
Morten, Brianna C.
Antony, Jisha
Henderson, Luke
Lasham, Annette
Campbell, Hamish
Cunliffe, Heather
Horsfield, Julia A.
Reddel, Roger R.
Avery-Kiejda, Kelly A.
Print, Cristin G.
Braithwaite, Antony W.
author_facet Mehta, Sunali Y.
Morten, Brianna C.
Antony, Jisha
Henderson, Luke
Lasham, Annette
Campbell, Hamish
Cunliffe, Heather
Horsfield, Julia A.
Reddel, Roger R.
Avery-Kiejda, Kelly A.
Print, Cristin G.
Braithwaite, Antony W.
author_sort Mehta, Sunali Y.
collection PubMed
description The TP53 family consists of three sets of transcription factor genes, TP53, TP63 and TP73, each of which expresses multiple RNA variants and protein isoforms. Of these, TP53 is mutated in 25-30% of breast cancers. How TP53 mutations affect the interaction of TP53 family members and their isoforms in breast cancer is unknown. To investigate this, 3 independent breast cancer cohorts were stratified into 4 groups based on oestrogen receptor (ER) and TP53 mutation status. Using bioinformatic methodologies, principal signalling pathways associated with the expression of TP53 family members were identified. Results show an enrichment of IFN-γ signalling associated with TP63 RNA in wild type TP53 (wtTP53), ER negative (ER-) tumours and with Δ133TP53 RNA in mutant TP53 (mTP53) ER positive (ER+) tumours. Moreover, tumours with low IFN-γ signalling were associated with significantly poorer patient outcome. The predicted changes in expression of a subset of RNAs involved in IFN-γ signalling were confirmed in vitro. Our data show that different members of the TP53 family can drive transcription of genes involved in IFN-γ signalling in different breast cancer subgroups.
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spelling pubmed-60443852018-07-17 Regulation of the interferon-gamma (IFN-γ) pathway by p63 and Δ133p53 isoform in different breast cancer subtypes Mehta, Sunali Y. Morten, Brianna C. Antony, Jisha Henderson, Luke Lasham, Annette Campbell, Hamish Cunliffe, Heather Horsfield, Julia A. Reddel, Roger R. Avery-Kiejda, Kelly A. Print, Cristin G. Braithwaite, Antony W. Oncotarget Research Paper The TP53 family consists of three sets of transcription factor genes, TP53, TP63 and TP73, each of which expresses multiple RNA variants and protein isoforms. Of these, TP53 is mutated in 25-30% of breast cancers. How TP53 mutations affect the interaction of TP53 family members and their isoforms in breast cancer is unknown. To investigate this, 3 independent breast cancer cohorts were stratified into 4 groups based on oestrogen receptor (ER) and TP53 mutation status. Using bioinformatic methodologies, principal signalling pathways associated with the expression of TP53 family members were identified. Results show an enrichment of IFN-γ signalling associated with TP63 RNA in wild type TP53 (wtTP53), ER negative (ER-) tumours and with Δ133TP53 RNA in mutant TP53 (mTP53) ER positive (ER+) tumours. Moreover, tumours with low IFN-γ signalling were associated with significantly poorer patient outcome. The predicted changes in expression of a subset of RNAs involved in IFN-γ signalling were confirmed in vitro. Our data show that different members of the TP53 family can drive transcription of genes involved in IFN-γ signalling in different breast cancer subgroups. Impact Journals LLC 2018-06-26 /pmc/articles/PMC6044385/ /pubmed/30018742 http://dx.doi.org/10.18632/oncotarget.25635 Text en Copyright: © 2018 Mehta et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Mehta, Sunali Y.
Morten, Brianna C.
Antony, Jisha
Henderson, Luke
Lasham, Annette
Campbell, Hamish
Cunliffe, Heather
Horsfield, Julia A.
Reddel, Roger R.
Avery-Kiejda, Kelly A.
Print, Cristin G.
Braithwaite, Antony W.
Regulation of the interferon-gamma (IFN-γ) pathway by p63 and Δ133p53 isoform in different breast cancer subtypes
title Regulation of the interferon-gamma (IFN-γ) pathway by p63 and Δ133p53 isoform in different breast cancer subtypes
title_full Regulation of the interferon-gamma (IFN-γ) pathway by p63 and Δ133p53 isoform in different breast cancer subtypes
title_fullStr Regulation of the interferon-gamma (IFN-γ) pathway by p63 and Δ133p53 isoform in different breast cancer subtypes
title_full_unstemmed Regulation of the interferon-gamma (IFN-γ) pathway by p63 and Δ133p53 isoform in different breast cancer subtypes
title_short Regulation of the interferon-gamma (IFN-γ) pathway by p63 and Δ133p53 isoform in different breast cancer subtypes
title_sort regulation of the interferon-gamma (ifn-γ) pathway by p63 and δ133p53 isoform in different breast cancer subtypes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044385/
https://www.ncbi.nlm.nih.gov/pubmed/30018742
http://dx.doi.org/10.18632/oncotarget.25635
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