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ARID1A/BAF250a is significantly overexpressed in primary invasive breast cancer

BACKGROUND: ARID1A (also known as BAF250a, p270 or SMARCF1) is a major component of the mammalian SWI/SNF family that is involved in the regulation of the chromatin structure. ARID1A gene mutations have been associated with many types of malignancies, including breast cancer. This study aimed to exp...

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Autores principales: Szpon, Łukasz, Agrawal, Anil, Jelen, Michal, Lipinski, Artur, Rudnicki, Jerzy, Makuch, Sebastian, Woźniak, Marta, Szmit, Mateusz, Agrawal, Siddarth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798264/
https://www.ncbi.nlm.nih.gov/pubmed/35117760
http://dx.doi.org/10.21037/tcr-19-2422
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author Szpon, Łukasz
Agrawal, Anil
Jelen, Michal
Lipinski, Artur
Rudnicki, Jerzy
Makuch, Sebastian
Woźniak, Marta
Szmit, Mateusz
Agrawal, Siddarth
author_facet Szpon, Łukasz
Agrawal, Anil
Jelen, Michal
Lipinski, Artur
Rudnicki, Jerzy
Makuch, Sebastian
Woźniak, Marta
Szmit, Mateusz
Agrawal, Siddarth
author_sort Szpon, Łukasz
collection PubMed
description BACKGROUND: ARID1A (also known as BAF250a, p270 or SMARCF1) is a major component of the mammalian SWI/SNF family that is involved in the regulation of the chromatin structure. ARID1A gene mutations have been associated with many types of malignancies, including breast cancer. This study aimed to explore the expression of BAF250a protein in breast cancer and its association with the clinical and pathological characteristics and prognosis of breast cancer. METHODS: We assessed the BAF250a expression in 119 invasive breast carcinomas samples and 92 healthy control and correlated this expression pattern with various clinical and pathologic parameters including histologic type and grade, tumor size, lymph node status, estrogen receptor (ER) status, progesterone receptor (PR) status. Immunohistochemical analysis of BAF250a, ER, PR, was carried out, and evaluation of stainings was performed. RESULTS: The mean value of BAF250a expression in the experimental group was higher than in healthy control (P=0.001). The expression is unrelated to age, menopausal status, lymph node status, tumor size and location, grade and histologic type of tumor, and hormonal status (ER, PR). CONCLUSIONS: These data suggest that BAF250a is overexpressed in breast cancers. BAF250a may play context-dependent tumor-promoting and tumor-suppressive roles in cancer.
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spelling pubmed-87982642022-02-02 ARID1A/BAF250a is significantly overexpressed in primary invasive breast cancer Szpon, Łukasz Agrawal, Anil Jelen, Michal Lipinski, Artur Rudnicki, Jerzy Makuch, Sebastian Woźniak, Marta Szmit, Mateusz Agrawal, Siddarth Transl Cancer Res Original Article BACKGROUND: ARID1A (also known as BAF250a, p270 or SMARCF1) is a major component of the mammalian SWI/SNF family that is involved in the regulation of the chromatin structure. ARID1A gene mutations have been associated with many types of malignancies, including breast cancer. This study aimed to explore the expression of BAF250a protein in breast cancer and its association with the clinical and pathological characteristics and prognosis of breast cancer. METHODS: We assessed the BAF250a expression in 119 invasive breast carcinomas samples and 92 healthy control and correlated this expression pattern with various clinical and pathologic parameters including histologic type and grade, tumor size, lymph node status, estrogen receptor (ER) status, progesterone receptor (PR) status. Immunohistochemical analysis of BAF250a, ER, PR, was carried out, and evaluation of stainings was performed. RESULTS: The mean value of BAF250a expression in the experimental group was higher than in healthy control (P=0.001). The expression is unrelated to age, menopausal status, lymph node status, tumor size and location, grade and histologic type of tumor, and hormonal status (ER, PR). CONCLUSIONS: These data suggest that BAF250a is overexpressed in breast cancers. BAF250a may play context-dependent tumor-promoting and tumor-suppressive roles in cancer. AME Publishing Company 2020-06 /pmc/articles/PMC8798264/ /pubmed/35117760 http://dx.doi.org/10.21037/tcr-19-2422 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Szpon, Łukasz
Agrawal, Anil
Jelen, Michal
Lipinski, Artur
Rudnicki, Jerzy
Makuch, Sebastian
Woźniak, Marta
Szmit, Mateusz
Agrawal, Siddarth
ARID1A/BAF250a is significantly overexpressed in primary invasive breast cancer
title ARID1A/BAF250a is significantly overexpressed in primary invasive breast cancer
title_full ARID1A/BAF250a is significantly overexpressed in primary invasive breast cancer
title_fullStr ARID1A/BAF250a is significantly overexpressed in primary invasive breast cancer
title_full_unstemmed ARID1A/BAF250a is significantly overexpressed in primary invasive breast cancer
title_short ARID1A/BAF250a is significantly overexpressed in primary invasive breast cancer
title_sort arid1a/baf250a is significantly overexpressed in primary invasive breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798264/
https://www.ncbi.nlm.nih.gov/pubmed/35117760
http://dx.doi.org/10.21037/tcr-19-2422
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