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HER2 Amplification in p53-Mutated Endometrial Carcinomas

SIMPLE SUMMARY: Endometrial cancers with p53 mutations tend to recur and develop metastases more frequently. From this point of view, the detection of new potential therapeutic targets such as HER2 is particularly interesting. In this study, we demonstrated that overexpression of HER2 (++ or +++) wa...

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Autores principales: Balestra, Ambre, Larsimont, Denis, Noël, Jean-Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10001224/
https://www.ncbi.nlm.nih.gov/pubmed/36900227
http://dx.doi.org/10.3390/cancers15051435
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author Balestra, Ambre
Larsimont, Denis
Noël, Jean-Christophe
author_facet Balestra, Ambre
Larsimont, Denis
Noël, Jean-Christophe
author_sort Balestra, Ambre
collection PubMed
description SIMPLE SUMMARY: Endometrial cancers with p53 mutations tend to recur and develop metastases more frequently. From this point of view, the detection of new potential therapeutic targets such as HER2 is particularly interesting. In this study, we demonstrated that overexpression of HER2 (++ or +++) was present in 31.4% of p53-mutated endometrial carcinomas and that among these, 36.3% showed amplification of the HER2 gene by CISH (Chromogenic In Situ Hybridization). These results suggest that various anti-HER2 agents could constitute interesting future treatments in this type of cancer. ABSTRACT: p53-mutated endometrial carcinomas tend to recur and develop distant metastases. Therefore, the detection of new potential therapeutic targets such as HER2 is particularly interesting. In this retrospective study, which considered over 118 endometrial carcinomas, the p53 mutation was detected in 29.6% of cases. In these cases, the HER2 protein profile was studied via immunohistochemistry, and an overexpression of HER2 protein (++ or +++) was noted in 31.4%. The CISH technique was used in these cases to determine if gene amplification was present. In 18% of cases, the technique was not conclusive. Amplification of the HER2 gene was observed in 36.3% of cases and 36.3% of cases showed a polysomal-like aneusomy for centromere 17. Amplification was found in serous carcinomas, clear cell carcinomas and carcinosarcomas, highlighting the future potentiality of HER2-targeted therapies in these variants of aggressive carcinomas.
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spelling pubmed-100012242023-03-11 HER2 Amplification in p53-Mutated Endometrial Carcinomas Balestra, Ambre Larsimont, Denis Noël, Jean-Christophe Cancers (Basel) Article SIMPLE SUMMARY: Endometrial cancers with p53 mutations tend to recur and develop metastases more frequently. From this point of view, the detection of new potential therapeutic targets such as HER2 is particularly interesting. In this study, we demonstrated that overexpression of HER2 (++ or +++) was present in 31.4% of p53-mutated endometrial carcinomas and that among these, 36.3% showed amplification of the HER2 gene by CISH (Chromogenic In Situ Hybridization). These results suggest that various anti-HER2 agents could constitute interesting future treatments in this type of cancer. ABSTRACT: p53-mutated endometrial carcinomas tend to recur and develop distant metastases. Therefore, the detection of new potential therapeutic targets such as HER2 is particularly interesting. In this retrospective study, which considered over 118 endometrial carcinomas, the p53 mutation was detected in 29.6% of cases. In these cases, the HER2 protein profile was studied via immunohistochemistry, and an overexpression of HER2 protein (++ or +++) was noted in 31.4%. The CISH technique was used in these cases to determine if gene amplification was present. In 18% of cases, the technique was not conclusive. Amplification of the HER2 gene was observed in 36.3% of cases and 36.3% of cases showed a polysomal-like aneusomy for centromere 17. Amplification was found in serous carcinomas, clear cell carcinomas and carcinosarcomas, highlighting the future potentiality of HER2-targeted therapies in these variants of aggressive carcinomas. MDPI 2023-02-24 /pmc/articles/PMC10001224/ /pubmed/36900227 http://dx.doi.org/10.3390/cancers15051435 Text en © 2023 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
Balestra, Ambre
Larsimont, Denis
Noël, Jean-Christophe
HER2 Amplification in p53-Mutated Endometrial Carcinomas
title HER2 Amplification in p53-Mutated Endometrial Carcinomas
title_full HER2 Amplification in p53-Mutated Endometrial Carcinomas
title_fullStr HER2 Amplification in p53-Mutated Endometrial Carcinomas
title_full_unstemmed HER2 Amplification in p53-Mutated Endometrial Carcinomas
title_short HER2 Amplification in p53-Mutated Endometrial Carcinomas
title_sort her2 amplification in p53-mutated endometrial carcinomas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10001224/
https://www.ncbi.nlm.nih.gov/pubmed/36900227
http://dx.doi.org/10.3390/cancers15051435
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