A meta-analysis of the relationship between FGFR3 and TP53 mutations in bladder cancer.

TP53 and FGFR3 mutations are the most common mutations in bladder cancers. FGFR3 mutations are most frequent in low-grade low-stage tumours, whereas TP53 mutations are most frequent in high-grade high-stage tumours. Several studies have reported FGFR3 and TP53 mutations to be mutually exclusive even...

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Autores principales: Yann Neuzillet, Xavier Paoletti, Slah Ouerhani, Pierre Mongiat-Artus, Hany Soliman, Hugues de The, Mathilde Sibony, Yves Denoux, Vincent Molinie, Aurélie Herault, May-Linda Lepage, Pascale Maille, Audrey Renou, Dimitri Vordos, Claude-Clément Abbou, Ashraf Bakkar, Bernard Asselain, Nadia Kourda, Amel El Gaaied, Karen Leroy, Agnès Laplanche, Simone Benhamou, Thierry Lebret, Yves Allory, François Radvanyi
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:53f5b53e570340e18b559b078466bd8a2021-11-18T08:05:14ZA meta-analysis of the relationship between FGFR3 and TP53 mutations in bladder cancer.1932-620310.1371/journal.pone.0048993https://doaj.org/article/53f5b53e570340e18b559b078466bd8a2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23272046/?tool=EBIhttps://doaj.org/toc/1932-6203TP53 and FGFR3 mutations are the most common mutations in bladder cancers. FGFR3 mutations are most frequent in low-grade low-stage tumours, whereas TP53 mutations are most frequent in high-grade high-stage tumours. Several studies have reported FGFR3 and TP53 mutations to be mutually exclusive events, whereas others have reported them to be independent. We carried out a meta-analysis of published findings for FGFR3 and TP53 mutations in bladder cancer (535 tumours, 6 publications) and additional unpublished data for 382 tumours. TP53 and FGFR3 mutations were not independent events for all tumours considered together (OR = 0.25 [0.18-0.37], p = 0.0001) or for pT1 tumours alone (OR = 0.47 [0.28-0.79], p = 0.0009). However, if the analysis was restricted to pTa tumours or to muscle-invasive tumours alone, FGFR3 and TP53 mutations were independent events (OR = 0.56 [0.23-1.36] (p = 0.12) and OR = 0.99 [0.37-2.7] (p = 0.35), respectively). After stratification of the tumours by stage and grade, no dependence was detected in the five tumour groups considered (pTaG1 and pTaG2 together, pTaG3, pT1G2, pT1G3, pT2-4). These differences in findings can be attributed to the putative existence of two different pathways of tumour progression in bladder cancer: the CIS pathway, in which FGFR3 mutations are rare, and the Ta pathway, in which FGFR3 mutations are frequent. TP53 mutations occur at the earliest stage of the CIS pathway, whereas they occur would much later in the Ta pathway, at the T1G3 or muscle-invasive stage.Yann NeuzilletXavier PaolettiSlah OuerhaniPierre Mongiat-ArtusHany SolimanHugues de TheMathilde SibonyYves DenouxVincent MolinieAurélie HeraultMay-Linda LepagePascale MailleAudrey RenouDimitri VordosClaude-Clément AbbouAshraf BakkarBernard AsselainNadia KourdaAmel El GaaiedKaren LeroyAgnès LaplancheSimone BenhamouThierry LebretYves AlloryFrançois RadvanyiPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 12, p e48993 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yann Neuzillet
Xavier Paoletti
Slah Ouerhani
Pierre Mongiat-Artus
Hany Soliman
Hugues de The
Mathilde Sibony
Yves Denoux
Vincent Molinie
Aurélie Herault
May-Linda Lepage
Pascale Maille
Audrey Renou
Dimitri Vordos
Claude-Clément Abbou
Ashraf Bakkar
Bernard Asselain
Nadia Kourda
Amel El Gaaied
Karen Leroy
Agnès Laplanche
Simone Benhamou
Thierry Lebret
Yves Allory
François Radvanyi
A meta-analysis of the relationship between FGFR3 and TP53 mutations in bladder cancer.
description TP53 and FGFR3 mutations are the most common mutations in bladder cancers. FGFR3 mutations are most frequent in low-grade low-stage tumours, whereas TP53 mutations are most frequent in high-grade high-stage tumours. Several studies have reported FGFR3 and TP53 mutations to be mutually exclusive events, whereas others have reported them to be independent. We carried out a meta-analysis of published findings for FGFR3 and TP53 mutations in bladder cancer (535 tumours, 6 publications) and additional unpublished data for 382 tumours. TP53 and FGFR3 mutations were not independent events for all tumours considered together (OR = 0.25 [0.18-0.37], p = 0.0001) or for pT1 tumours alone (OR = 0.47 [0.28-0.79], p = 0.0009). However, if the analysis was restricted to pTa tumours or to muscle-invasive tumours alone, FGFR3 and TP53 mutations were independent events (OR = 0.56 [0.23-1.36] (p = 0.12) and OR = 0.99 [0.37-2.7] (p = 0.35), respectively). After stratification of the tumours by stage and grade, no dependence was detected in the five tumour groups considered (pTaG1 and pTaG2 together, pTaG3, pT1G2, pT1G3, pT2-4). These differences in findings can be attributed to the putative existence of two different pathways of tumour progression in bladder cancer: the CIS pathway, in which FGFR3 mutations are rare, and the Ta pathway, in which FGFR3 mutations are frequent. TP53 mutations occur at the earliest stage of the CIS pathway, whereas they occur would much later in the Ta pathway, at the T1G3 or muscle-invasive stage.
format article
author Yann Neuzillet
Xavier Paoletti
Slah Ouerhani
Pierre Mongiat-Artus
Hany Soliman
Hugues de The
Mathilde Sibony
Yves Denoux
Vincent Molinie
Aurélie Herault
May-Linda Lepage
Pascale Maille
Audrey Renou
Dimitri Vordos
Claude-Clément Abbou
Ashraf Bakkar
Bernard Asselain
Nadia Kourda
Amel El Gaaied
Karen Leroy
Agnès Laplanche
Simone Benhamou
Thierry Lebret
Yves Allory
François Radvanyi
author_facet Yann Neuzillet
Xavier Paoletti
Slah Ouerhani
Pierre Mongiat-Artus
Hany Soliman
Hugues de The
Mathilde Sibony
Yves Denoux
Vincent Molinie
Aurélie Herault
May-Linda Lepage
Pascale Maille
Audrey Renou
Dimitri Vordos
Claude-Clément Abbou
Ashraf Bakkar
Bernard Asselain
Nadia Kourda
Amel El Gaaied
Karen Leroy
Agnès Laplanche
Simone Benhamou
Thierry Lebret
Yves Allory
François Radvanyi
author_sort Yann Neuzillet
title A meta-analysis of the relationship between FGFR3 and TP53 mutations in bladder cancer.
title_short A meta-analysis of the relationship between FGFR3 and TP53 mutations in bladder cancer.
title_full A meta-analysis of the relationship between FGFR3 and TP53 mutations in bladder cancer.
title_fullStr A meta-analysis of the relationship between FGFR3 and TP53 mutations in bladder cancer.
title_full_unstemmed A meta-analysis of the relationship between FGFR3 and TP53 mutations in bladder cancer.
title_sort meta-analysis of the relationship between fgfr3 and tp53 mutations in bladder cancer.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/53f5b53e570340e18b559b078466bd8a
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