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Clinical Implications of Androgen-Positive Triple-Negative Breast Cancer

SIMPLE SUMMARY: Triple-negative breast cancer (TNBC) represents a heterogeneous group of breast cancers that lack estrogen receptor (ER), progesterone receptor (PR), and human epidermal factor 2 (HER2) amplifications. This triple negativity represents a challenge in choosing the right treatment, as...

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Autores principales: Brumec, Maša, Sobočan, Monika, Takač, Iztok, Arko, Darja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037213/
https://www.ncbi.nlm.nih.gov/pubmed/33915941
http://dx.doi.org/10.3390/cancers13071642
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author Brumec, Maša
Sobočan, Monika
Takač, Iztok
Arko, Darja
author_facet Brumec, Maša
Sobočan, Monika
Takač, Iztok
Arko, Darja
author_sort Brumec, Maša
collection PubMed
description SIMPLE SUMMARY: Triple-negative breast cancer (TNBC) represents a heterogeneous group of breast cancers that lack estrogen receptor (ER), progesterone receptor (PR), and human epidermal factor 2 (HER2) amplifications. This triple negativity represents a challenge in choosing the right treatment, as without the aforementioned biomarkers there are no efficient therapeutic targets. Nevertheless, some triple-negative breast cancers express androgen receptor (AR), which could be used as a novel therapeutic target in such subgroup of breast cancers. In our review, we aimed to identify clinical features and proposed potential therapeutic approaches of this specific subgroup—AR-positive triple-negative breast cancer. Our findings contributed to a better understanding of the current problematics regarding AR-positive TNBC. ABSTRACT: This review summarizes the recent findings of a vast array of studies conducted on androgen receptor-positive triple-negative breast cancer (AR-positive TNBC) to provide a better understanding of this specific breast cancer subgroup. AR expression is correlated with higher age, lower histological grade, lower proliferation index Ki-67, spiculated masses, and calcifications on mammography. Studies investigating the correlation between AR expression and lymph node metastasis are highly discordant. In addition, results regarding prognosis are highly contradictory. AR antagonists are a promising novel therapeutic approach in AR-positive TNBC. However, AR signaling pathways should be more investigated in order to understand the influence of AR expression on TNBC more thoroughly.
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spelling pubmed-80372132021-04-12 Clinical Implications of Androgen-Positive Triple-Negative Breast Cancer Brumec, Maša Sobočan, Monika Takač, Iztok Arko, Darja Cancers (Basel) Review SIMPLE SUMMARY: Triple-negative breast cancer (TNBC) represents a heterogeneous group of breast cancers that lack estrogen receptor (ER), progesterone receptor (PR), and human epidermal factor 2 (HER2) amplifications. This triple negativity represents a challenge in choosing the right treatment, as without the aforementioned biomarkers there are no efficient therapeutic targets. Nevertheless, some triple-negative breast cancers express androgen receptor (AR), which could be used as a novel therapeutic target in such subgroup of breast cancers. In our review, we aimed to identify clinical features and proposed potential therapeutic approaches of this specific subgroup—AR-positive triple-negative breast cancer. Our findings contributed to a better understanding of the current problematics regarding AR-positive TNBC. ABSTRACT: This review summarizes the recent findings of a vast array of studies conducted on androgen receptor-positive triple-negative breast cancer (AR-positive TNBC) to provide a better understanding of this specific breast cancer subgroup. AR expression is correlated with higher age, lower histological grade, lower proliferation index Ki-67, spiculated masses, and calcifications on mammography. Studies investigating the correlation between AR expression and lymph node metastasis are highly discordant. In addition, results regarding prognosis are highly contradictory. AR antagonists are a promising novel therapeutic approach in AR-positive TNBC. However, AR signaling pathways should be more investigated in order to understand the influence of AR expression on TNBC more thoroughly. MDPI 2021-04-01 /pmc/articles/PMC8037213/ /pubmed/33915941 http://dx.doi.org/10.3390/cancers13071642 Text en © 2021 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 Review
Brumec, Maša
Sobočan, Monika
Takač, Iztok
Arko, Darja
Clinical Implications of Androgen-Positive Triple-Negative Breast Cancer
title Clinical Implications of Androgen-Positive Triple-Negative Breast Cancer
title_full Clinical Implications of Androgen-Positive Triple-Negative Breast Cancer
title_fullStr Clinical Implications of Androgen-Positive Triple-Negative Breast Cancer
title_full_unstemmed Clinical Implications of Androgen-Positive Triple-Negative Breast Cancer
title_short Clinical Implications of Androgen-Positive Triple-Negative Breast Cancer
title_sort clinical implications of androgen-positive triple-negative breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037213/
https://www.ncbi.nlm.nih.gov/pubmed/33915941
http://dx.doi.org/10.3390/cancers13071642
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