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Androgen receptor in estrogen receptor positive breast cancer: Beyond expression

Basile D.
•
Cinausero M.
•
Iacono D.
altro
Puglisi F.
2017
  • journal article

Periodico
CANCER TREATMENT REVIEWS
Abstract
In recent years, new therapeutic approaches have reshaped the overall strategy of breast cancer (BC) treatment and have markedly improved patient survival. This is, in part, due to novel therapies for estrogen receptor (ER)-positive BC. Unfortunately, many patients present de novo resistance to these therapies or develop an acquired resistance over time. Therefore, research is now focused on discovering new molecular targets to overcome these resistances. Interestingly, preclinical and clinical studies have shown a critical role for the cross-talk between androgen receptor (AR) and ER in luminal-like BC. AR is expressed in >60% of BC and in up to 90% of ERα-positive tumors. Multiple studies suggest that AR is associated with a favorable prognosis. However, AR overexpression and, in particular, the high AR:ER ratio, seem to be involved in resistance to hormonal treatment. In this setting, a group of BCs could benefit from AR-inhibitors; nevertheless, some ER-positive BC patients do not seem to benefit from this strategy. Therefore, it is crucial to identify biomarkers that would enable the selection of patients who might benefit from combination treatment with ER and AR inhibitors.
DOI
10.1016/j.ctrv.2017.09.006
WOS
WOS:000417666200003
Archivio
http://hdl.handle.net/11390/1159671
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85032026200
http://www.elsevier.com/inca/publications/store/6/2/3/0/2/2/index.htt
Diritti
metadata only access
Soggetti
  • Androgen receptor

  • Anti-androgen therapy...

  • Breast cancer

  • Endocrine resistance

  • Animal

  • Breast Neoplasm

  • Female

  • Human

  • Receptors, Androgen

  • Receptors, Estrogen

Scopus© citazioni
29
Data di acquisizione
Jun 7, 2022
Vedi dettagli
Web of Science© citazioni
40
Data di acquisizione
Mar 27, 2024
Visualizzazioni
1
Data di acquisizione
Apr 19, 2024
Vedi dettagli
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