Androgen receptor expression in breast cancer: Implications on prognosis and treatment, a brief review.
Androgen receptor
Anti-androgens
Breast cancer
Predictive factor
Prognostic factor
and therapeutic target
Journal
Molecular and cellular endocrinology
ISSN: 1872-8057
Titre abrégé: Mol Cell Endocrinol
Pays: Ireland
ID NLM: 7500844
Informations de publication
Date de publication:
01 07 2021
01 07 2021
Historique:
received:
23
11
2020
revised:
28
04
2021
accepted:
10
05
2021
pubmed:
18
5
2021
medline:
15
12
2021
entrez:
17
5
2021
Statut:
ppublish
Résumé
Approximately 70%-85% of breast cancers express androgen receptors (ARs). The role of AR in breast cancer pathogenesis is currently in exploration. Both androgens and anti-androgens have demonstrated variable inhibitory and stimulatory effects in AR-positive breast cancer depending on estrogen receptor and HER2 co-expression. Androgen signaling pathways interact with other critical cellular pathways, such as the PI3K/AKT/mTOR, Ras/Raf/MAPK/ERK, Wnt/β-catenin, and estrogen signaling pathways. Therapeutic exploitation of AR has been the crux of management of prostate cancer for decades. In recent years there has been increasing interest in AR as a novel therapeutic target in breast cancer. There have been many early phase clinical trials evaluating the safety and efficacy of various AR-targeted agents in breast cancer. Some of these studies have shown promising clinical benefits. Studies of biomarkers to identify the patients likely to benefit from AR-targeted therapies are currently in progress. Besides, AR expression may be an important prognostic and predictive marker for breast cancer, which needs to be defined better in future studies.
Identifiants
pubmed: 34000352
pii: S0303-7207(21)00168-4
doi: 10.1016/j.mce.2021.111324
pii:
doi:
Substances chimiques
AR protein, human
0
Antineoplastic Agents
0
Receptors, Androgen
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
111324Informations de copyright
Copyright © 2021 Elsevier B.V. All rights reserved.