Targeting the androgen receptor in prostate and breast cancer: several new agents in development

Tracy Proverbs-Singh1, Jarett L Feldman1, Michael J Morris2

  • 1Breast Medicine ServiceDepartment of Medicine, Memorial Sloan Kettering Cancer Center, 300 East 66th Street, New York, New York 10065, USAGenitourinary Oncology ServiceDepartment of Medicine, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, New York 10065, USAWeill Cornell Medical College1300 York Avenue, New York, New York 10065, USA.

Endocrine-Related Cancer
|February 28, 2015
PubMed

Insights

Androgen receptor (AR) signaling is key in prostate cancer (PCa) and increasingly recognized in breast cancer (BCa). This review covers current and novel AR-targeting therapies for both hormone-sensitive cancers.

Area of Science:

  • Oncology
  • Endocrinology
  • Molecular Biology

Background:

  • Prostate cancer (PCa) and breast cancer (BCa) are hormone-sensitive malignancies with complex biology.
  • The androgen receptor (AR) pathway is crucial in PCa and shows emerging relevance in BCa.
  • AR is co-expressed with other key receptors (ER, PR, HER2) across BCa subtypes.

Purpose of the Study:

  • To review current and emerging therapies targeting the androgen receptor (AR) axis.
  • To explore the role of AR in both prostate cancer and breast cancer.
  • To provide insights into novel drug development for AR-targeted treatments.

Main Methods:

  • Literature review of existing and investigational therapies.
  • Analysis of AR pathway involvement in PCa and BCa.
  • Synthesis of data on AR co-expression in breast cancer subtypes.

Main Results:

  • Androgen synthesis and AR pathway inhibition are established PCa treatments.
  • AR plays a role in BCa development and growth, irrespective of subtype.
  • Novel AR-targeting agents are under development for potential dual application.

Conclusions:

  • The AR axis represents a promising therapeutic target for both PCa and BCa.
  • Targeting AR offers a potential strategy to overcome treatment resistance in hormone-sensitive cancers.
  • Further research into novel AR-targeted therapies could benefit patients with both cancer types.

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