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Androgen receptor signalling in non-prostatic malignancies: challenges and opportunities. | LitMetric

Androgen receptor signalling in non-prostatic malignancies: challenges and opportunities.

Nat Rev Cancer

Service d'Oto-rhino-laryngologie et chirurgie cervical faciale, Centre Hospitalier Universitaire Vaudois (CHUV), Université de Lausanne (UNIL), Lausanne, Switzerland.

Published: November 2024

AI Article Synopsis

  • The androgen receptor (AR) pathway is well-researched in prostate cancer but less so in other cancers, despite AR being present and active in those areas.
  • The review highlights the potential benefits of targeting AR in various cancers, despite its complex role in both promoting and suppressing cancer progression.
  • Future studies are needed to understand how AR influences cancer biology and to create targeted treatments for patients with non-prostatic cancers, which may include modulating immune responses.

Article Abstract

The androgen receptor (AR) signalling pathway has been intensively studied in the context of prostate cancer, where androgen deprivation therapy is part of the standard of care for metastatic disease. By contrast, fewer studies have investigated the impact and translational potential of targeting AR in other cancer types where it is also expressed and functional. In this Review, we discuss the current understanding of AR in non-prostatic cancer types and summarize ongoing AR-directed clinical trials. While different androgen levels contribute to sexual dimorphism in cancer, targeting the AR system could benefit both sexes and help overcome resistance to targeted therapies. However, a bimodal function of AR signalling, which suppresses stromal changes associated with the early stages of cancer development, also needs to be considered. Future research is necessary to scrutinize cellular and molecular mechanisms of action of AR in cancer cells and the tumour microenvironment, to develop selective modulators of AR activity, and to identify patients with non-prostatic cancer who might benefit from targeting this pathway. AR-directed manipulation of host immune cells may offer a promising therapeutic approach for many types of cancers.

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Source
http://dx.doi.org/10.1038/s41568-024-00772-wDOI Listing

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