Androgen Receptor and PIM1 Expression in Tumor Tissue of Patients With Triple-negative Breast Cancer

Aliki Ntzifa1, Areti Strati1, Georgia-Angeliki Koliou2

  • 1Analysis of Circulating Tumor Cells Laboratory, Laboratory of Analytical Chemistry, Department of Chemistry, University of Athens, Athens, Greece.

Abstract

Insights

Androgen receptor (AR) and PIM1 kinase co-expression is rare in triple-negative breast cancer (TNBC). This study found no significant prognostic value for AR or PIM1 in TNBC patient survival.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Triple-negative breast cancer (TNBC) lacks effective targeted therapies.
  • Androgen receptor (AR) and PIM1 kinase are implicated in a subset of TNBC.
  • PIM1 kinases regulate AR transcriptional activity, independent of androgens.

Purpose of the Study:

  • To evaluate the expression of AR and PIM1 in TNBC.
  • To determine the prognostic significance of AR and PIM1 in TNBC.

Main Methods:

  • Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used.
  • AR and PIM1 transcripts were measured in formalin-fixed paraffin-embedded tumor samples.
  • 141 TNBC patients were included in the study.

Main Results:

  • AR was expressed in 38.3% of TNBC cases.
  • PIM1 was expressed in 10.6% of TNBC cases.
  • Co-expression of AR and PIM1 was found in only 5.0% of patients (7/141).
  • Neither AR nor PIM1 expression showed prognostic significance for overall or disease-free survival.

Conclusions:

  • Co-expression of AR and PIM1 is infrequent in TNBC.
  • Further research in larger cohorts is needed to explore the therapeutic implications of AR and PIM1 in TNBC management.

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