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ARID1A in cancer: Friend or foe?

ARID1A belongs to a class of chromatin regulatory proteins that function by maintaining accessibility at most promoters and enhancers, thereby regulating gene expression. The high frequency of ARID1A alterations in human cancers has highlighted its significance in tumorigenesis. The precise role of...

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Autores principales: Fontana, Beatrice, Gallerani, Giulia, Salamon, Irene, Pace, Ilaria, Roncarati, Roberta, Ferracin, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987588/
https://www.ncbi.nlm.nih.gov/pubmed/36890819
http://dx.doi.org/10.3389/fonc.2023.1136248
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author Fontana, Beatrice
Gallerani, Giulia
Salamon, Irene
Pace, Ilaria
Roncarati, Roberta
Ferracin, Manuela
author_facet Fontana, Beatrice
Gallerani, Giulia
Salamon, Irene
Pace, Ilaria
Roncarati, Roberta
Ferracin, Manuela
author_sort Fontana, Beatrice
collection PubMed
description ARID1A belongs to a class of chromatin regulatory proteins that function by maintaining accessibility at most promoters and enhancers, thereby regulating gene expression. The high frequency of ARID1A alterations in human cancers has highlighted its significance in tumorigenesis. The precise role of ARID1A in cancer is highly variable since ARID1A alterations can have a tumor suppressive or oncogenic role, depending on the tumor type and context. ARID1A is mutated in about 10% of all tumor types including endometrial, bladder, gastric, liver, biliopancreatic cancer, some ovarian cancer subtypes, and the extremely aggressive cancers of unknown primary. Its loss is generally associated with disease progression more often than onset. In some cancers, ARID1A loss is associated with worse prognostic features, thus supporting a major tumor suppressive role. However, some exceptions have been reported. Thus, the association of ARID1A genetic alterations with patient prognosis is controversial. However, ARID1A loss of function is considered conducive for the use of inhibitory drugs which are based on synthetic lethality mechanisms. In this review we summarize the current knowledge on the role of ARID1A as tumor suppressor or oncogene in different tumor types and discuss the strategies for treating ARID1A mutated cancers.
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spelling pubmed-99875882023-03-07 ARID1A in cancer: Friend or foe? Fontana, Beatrice Gallerani, Giulia Salamon, Irene Pace, Ilaria Roncarati, Roberta Ferracin, Manuela Front Oncol Oncology ARID1A belongs to a class of chromatin regulatory proteins that function by maintaining accessibility at most promoters and enhancers, thereby regulating gene expression. The high frequency of ARID1A alterations in human cancers has highlighted its significance in tumorigenesis. The precise role of ARID1A in cancer is highly variable since ARID1A alterations can have a tumor suppressive or oncogenic role, depending on the tumor type and context. ARID1A is mutated in about 10% of all tumor types including endometrial, bladder, gastric, liver, biliopancreatic cancer, some ovarian cancer subtypes, and the extremely aggressive cancers of unknown primary. Its loss is generally associated with disease progression more often than onset. In some cancers, ARID1A loss is associated with worse prognostic features, thus supporting a major tumor suppressive role. However, some exceptions have been reported. Thus, the association of ARID1A genetic alterations with patient prognosis is controversial. However, ARID1A loss of function is considered conducive for the use of inhibitory drugs which are based on synthetic lethality mechanisms. In this review we summarize the current knowledge on the role of ARID1A as tumor suppressor or oncogene in different tumor types and discuss the strategies for treating ARID1A mutated cancers. Frontiers Media S.A. 2023-02-20 /pmc/articles/PMC9987588/ /pubmed/36890819 http://dx.doi.org/10.3389/fonc.2023.1136248 Text en Copyright © 2023 Fontana, Gallerani, Salamon, Pace, Roncarati and Ferracin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Fontana, Beatrice
Gallerani, Giulia
Salamon, Irene
Pace, Ilaria
Roncarati, Roberta
Ferracin, Manuela
ARID1A in cancer: Friend or foe?
title ARID1A in cancer: Friend or foe?
title_full ARID1A in cancer: Friend or foe?
title_fullStr ARID1A in cancer: Friend or foe?
title_full_unstemmed ARID1A in cancer: Friend or foe?
title_short ARID1A in cancer: Friend or foe?
title_sort arid1a in cancer: friend or foe?
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987588/
https://www.ncbi.nlm.nih.gov/pubmed/36890819
http://dx.doi.org/10.3389/fonc.2023.1136248
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