mRNA ratios of AR to ESR1 and PGR distinguish breast cancer subtypes based on public datasets and experimental models Academic Article

abstract

  • The role of the androgen receptor (AR) in breast cancer (BC) remains incompletely understood. Here, we conducted a meta-analysis of large-scale microarray transcriptomic datasets to evaluate whether the mRNA expression levels of the androgen receptor gene, relative to those of the estrogen receptor gene (AR/ESR1 ratio) and the progesterone receptor gene (AR/PGR ratio), can help differentiate BC tumor subtypes. Additionally, we used qRT-PCR assays to assess the mRNA levels of the AR/ESR1 and AR/PGR ratios in four cell lines representative of different BC subtypes (MCF7, BT474, MDA-MB453, and MDA-MB231), as well as in breast tissue from a small group of patients (11 cases) stratified by estrogen receptor (ER) status. Our results showed that higher AR gene expression relative to ESR1 and PGR (ampersand-flag-changege; 2.0 and ampersand-flag-changege; 1.54, respectively) were associated with BC patients classified under the Luminal B and HER2-enriched subtypes. Positive values of AR/ESR1 and AR/PGR ratios were also observed in the ER-negative (ER-) cell line MDA-MB453, as well as in tumor tissue from ER- BC patients. Our findings confirm that higher or even positive AR/ESR1 and AR/PGR ratios may be associated with BC cases exhibiting more aggressive clinical and biological features, leading to a worse prognosis.

publication date

  • 2025-12-1

edition

  • 15

keywords

  • Androgen Receptor
  • Androgen Receptor Gene
  • BT-474
  • Biological Characteristics
  • Breast Cancer
  • Breast Cancer Cases
  • Breast Cancer Patients
  • Breast Cancer Subtypes
  • Breast Tissue
  • Breast Tumor
  • Cell Line
  • Clinical Features
  • Estrogen Receptor
  • Estrogen Receptor 1 (ESR1)
  • Estrogen Receptor Gene
  • Estrogen Receptor Status
  • Estrogen Receptor-negative
  • Experimental Model
  • Gene Expression
  • HER2-enriched Subtype
  • Luminal B
  • MCF-7
  • MDA-MB-231
  • MRNA Level
  • Messenger RNA
  • Meta-Analysis
  • Meta-analysis
  • Microarray
  • Progesterone Receptor
  • Progesterone Receptor Gene
  • Public Dataset
  • QPCR Assay
  • Quantitative Reverse Transcription Polymerase Chain Reaction
  • Receptor Cells
  • Receptor Gene
  • Transcriptomic Data
  • Transcriptomics
  • Tumor Subtype
  • Tumor Tissue
  • Worse Prognosis
  • mRNA Expression Level