Androgen receptor expression in triple negative breast cancer: an Algerian population study

Amel Hedjem1, Amal Kouchkar2, Amel Ladjeroud3

  • 1Department of Biology, Faculty of Sciences, University M'hamed Bougara, Boumerdes, Algeria.

PubMed

Insights

Androgen receptor (AR) expression is found in a subset of triple-negative breast cancer (TNBC) patients. While AR positivity correlates with lower proliferation, it does not impact overall survival in this early-stage TNBC cohort.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • Triple-negative breast cancer (TNBC) lacks targeted therapies due to its heterogeneity.
  • The Luminal Androgen Receptor (LAR) TNBC subtype expresses the androgen receptor (AR), offering potential therapeutic avenues.

Purpose of the Study:

  • To evaluate androgen receptor (AR) expression in early-stage triple-negative breast cancer (TNBC).
  • To correlate AR expression with clinicopathological factors and patient survival.

Main Methods:

  • Retrospective analysis of 160 early-stage TNBC patients treated between February 2015 and February 2017.
  • Assessment of AR expression levels (≥1% and ≥10% positivity).
  • Correlation analysis with Ki-67 index, basal immunophenotype, and five-year overall survival.

Main Results:

  • Androgen receptor (AR) expression was detected in 16.87% (≥1% positivity) and 12.5% (≥10% positivity) of TNBC cases.
  • Positive AR expression showed an inverse correlation with high Ki-67 proliferation index and basal immunophenotype.
  • No significant association was found between AR expression and the five-year overall survival rate (p=0.77).

Conclusions:

  • Androgen receptor (AR) expression is a feature in a subset of triple-negative breast cancer (TNBC).
  • AR expression is linked to less aggressive tumor characteristics (lower proliferation, non-basal phenotype).
  • Current findings suggest AR expression may not be a prognostic marker for overall survival in early-stage TNBC, but warrants further investigation for therapeutic targeting.

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