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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.
Background/Aim:
Effective targeted therapies for triple-negative breast cancer (TNBC) are limited. In a subset of TNBC, androgen receptor (AR) plays an important role, while the human proviral integration site for Moloney murine leukemia virus-1 (PIM1) overexpression is also implicated. PIM1 kinases phosphorylate AR, thus regulating its transcriptional activity, regardless of the presence or not of androgens. We evaluated the expression of AR and PIM1 and their prognostic significance in TNBC.
Materials And Methods:
AR and PIM1 transcripts were quantified by quantitative reverse transcription polymerase chain reaction in formalin-fixed paraffin-embedded tumor from 141 patients with TNBC.
Results:
AR was expressed in 38.3%, PIM1 in 10.6%, while co-expression of AR and PIM1 was detected in 7/141 cases (5.0%). No prognostic significance of AR or PIM1 was reached for overall or disease-free survival.
Conclusion:
Co-expression of AR and PIM1 exists in only in a small percentage of patients with TNBC. The implications of this finding in the therapeutic management of patients with TNBC should be investigated in larger patient cohorts.
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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