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Relevance of ARID1A Mutations in Endometrial Carcinomas

Since the Cancer Genome Atlas (TCGA) project identified four distinct groups based on molecular alterations, mutation analyses have been integrated into the characterization of endometrial carcinomas (ECs). ARID1A seems to be the subunit more involved in the loss of function of the SWI/SNF complex i...

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Autores principales: De Leo, Antonio, Ravegnini, Gloria, Musiani, Francesco, Maloberti, Thais, Visani, Michela, Sanza, Viviana, Angelini, Sabrina, Perrone, Anna Myriam, De Iaco, Pierandrea, Corradini, Angelo Gianluca, Rosini, Francesca, Grillini, Marco, Santini, Donatella, Ceccarelli, Claudio, Zamagni, Claudio, Tallini, Giovanni, de Biase, Dario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947028/
https://www.ncbi.nlm.nih.gov/pubmed/35328145
http://dx.doi.org/10.3390/diagnostics12030592
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author De Leo, Antonio
Ravegnini, Gloria
Musiani, Francesco
Maloberti, Thais
Visani, Michela
Sanza, Viviana
Angelini, Sabrina
Perrone, Anna Myriam
De Iaco, Pierandrea
Corradini, Angelo Gianluca
Rosini, Francesca
Grillini, Marco
Santini, Donatella
Ceccarelli, Claudio
Zamagni, Claudio
Tallini, Giovanni
de Biase, Dario
author_facet De Leo, Antonio
Ravegnini, Gloria
Musiani, Francesco
Maloberti, Thais
Visani, Michela
Sanza, Viviana
Angelini, Sabrina
Perrone, Anna Myriam
De Iaco, Pierandrea
Corradini, Angelo Gianluca
Rosini, Francesca
Grillini, Marco
Santini, Donatella
Ceccarelli, Claudio
Zamagni, Claudio
Tallini, Giovanni
de Biase, Dario
author_sort De Leo, Antonio
collection PubMed
description Since the Cancer Genome Atlas (TCGA) project identified four distinct groups based on molecular alterations, mutation analyses have been integrated into the characterization of endometrial carcinomas (ECs). ARID1A seems to be the subunit more involved in the loss of function of the SWI/SNF complex in ECs. The aim of this study is to define the relevance of ARID1A alterations in a cohort of EC, studying the possible associations between DNA mutation (genomic level), RNA expression (transcriptomic level), and protein expression (proteomic level). A total of 50 endometrial carcinomas were characterized for ARID1A mutations (using targeted DNA next-generation sequencing—NGS), ARID1A gene expression (using RNAseq and qRT-PCR), and ARID1A protein expression (using immunohistochemistry—IHC). Moreover, we have investigated if ARID1A mutations may alter the protein structure, using the Protein Data Bank sequence. We found a good correlation between ARID1A mutations and protein immunostaining, even if we did not find statistically significant differences in the ARID1A expression levels. In conclusion, our data demonstrated that the molecular characterization of ARID1A should be associated with IHC analysis, mainly in those cases harboring “novel” ARID1A mutations or in those alterations with “uncertain” pathogenic significance.
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spelling pubmed-89470282022-03-25 Relevance of ARID1A Mutations in Endometrial Carcinomas De Leo, Antonio Ravegnini, Gloria Musiani, Francesco Maloberti, Thais Visani, Michela Sanza, Viviana Angelini, Sabrina Perrone, Anna Myriam De Iaco, Pierandrea Corradini, Angelo Gianluca Rosini, Francesca Grillini, Marco Santini, Donatella Ceccarelli, Claudio Zamagni, Claudio Tallini, Giovanni de Biase, Dario Diagnostics (Basel) Article Since the Cancer Genome Atlas (TCGA) project identified four distinct groups based on molecular alterations, mutation analyses have been integrated into the characterization of endometrial carcinomas (ECs). ARID1A seems to be the subunit more involved in the loss of function of the SWI/SNF complex in ECs. The aim of this study is to define the relevance of ARID1A alterations in a cohort of EC, studying the possible associations between DNA mutation (genomic level), RNA expression (transcriptomic level), and protein expression (proteomic level). A total of 50 endometrial carcinomas were characterized for ARID1A mutations (using targeted DNA next-generation sequencing—NGS), ARID1A gene expression (using RNAseq and qRT-PCR), and ARID1A protein expression (using immunohistochemistry—IHC). Moreover, we have investigated if ARID1A mutations may alter the protein structure, using the Protein Data Bank sequence. We found a good correlation between ARID1A mutations and protein immunostaining, even if we did not find statistically significant differences in the ARID1A expression levels. In conclusion, our data demonstrated that the molecular characterization of ARID1A should be associated with IHC analysis, mainly in those cases harboring “novel” ARID1A mutations or in those alterations with “uncertain” pathogenic significance. MDPI 2022-02-25 /pmc/articles/PMC8947028/ /pubmed/35328145 http://dx.doi.org/10.3390/diagnostics12030592 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
De Leo, Antonio
Ravegnini, Gloria
Musiani, Francesco
Maloberti, Thais
Visani, Michela
Sanza, Viviana
Angelini, Sabrina
Perrone, Anna Myriam
De Iaco, Pierandrea
Corradini, Angelo Gianluca
Rosini, Francesca
Grillini, Marco
Santini, Donatella
Ceccarelli, Claudio
Zamagni, Claudio
Tallini, Giovanni
de Biase, Dario
Relevance of ARID1A Mutations in Endometrial Carcinomas
title Relevance of ARID1A Mutations in Endometrial Carcinomas
title_full Relevance of ARID1A Mutations in Endometrial Carcinomas
title_fullStr Relevance of ARID1A Mutations in Endometrial Carcinomas
title_full_unstemmed Relevance of ARID1A Mutations in Endometrial Carcinomas
title_short Relevance of ARID1A Mutations in Endometrial Carcinomas
title_sort relevance of arid1a mutations in endometrial carcinomas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947028/
https://www.ncbi.nlm.nih.gov/pubmed/35328145
http://dx.doi.org/10.3390/diagnostics12030592
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