Androgen Receptor Expression in Early Triple-Negative Breast Cancer: Clinical Significance and Prognostic Associations
Creators
- 1. Clinica di Oncologia Medica, AO Ospedali Riuniti-Ancona, Università Politecnica delle Marche, Ancona 60020 (Italy)
- 2. Anatomia Patologica, AO Ospedali Riuniti-Ancona, Università Politecnica delle Marche, Ancona 60020 (Italy)
Description
Background: Triple-negative breast cancers (TNBC) are characterized by aggressive tumour biology resulting in a poor prognosis. Androgen receptor (AR) is one of newly emerging biomarker in TNBC. In recent years, ARs have been demonstrated to play an important role in the genesis and in the development of breast cancer, although their prognostic role is still debated. In the present study, we explored the correlation of AR expression with clinical, pathological and molecular features and its impact on prognosis in early TNBC. Patients and Methods: ARs were considered positive in case of tumors with >10% nuclear-stained. Survival distribution was estimated by the Kaplan Meier method. The univariate and multivariate analyses were performed. The difference among variables were calculated by chi-square test. Results: 81 TNBC patients diagnosed between January 2006 and December 2011 were included in the analysis. Slides were stained immunohistochemically for estrogen and progesterone receptors, HER-2, Ki-67, ALDH1, e-cadherin and AR. Of the 81 TNBC samples, 18.8% showed positive immunostaining for AR, 23.5% and 44.4% of patients were negative for e-cadherin and ALDH1, respectively. Positive AR immunostaining was inversely correlated with a higher Ki-67 (p < 0.0001) and a lympho-vascular invasion (p = 0.01), but no other variables. Univariate survival analysis revealed that AR expression was not associated with disease-free survival (p = 0.72) or overall survival (p = 0.93). Conclusions: The expression of AR is associated with some biological features of TNBC, such as Ki-67 and lympho-vascular invasion; nevertheless the prognostic significance of AR was not documented in our analysis. However, since ARs are expressed in a significant number of TNBC, prospective studies in order to determine the biological mechanisms and their potential role as novel treatment target
Availability note (English)
Available from http://dx.doi.org/10.3390/cancers6031351; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190544Additional details
Identifiers
Publishing Information
- Journal Title
- Cancers (Basel)
- Journal Volume
- 6
- Journal Issue
- 3
- Journal Page Range
- p. 1351-1362
- ISSN
- 2072-6694
INIS
- Country of Publication
- Switzerland
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47006759
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ANDROGENS; MAMMARY GLANDS; MULTIVARIATE ANALYSIS; NEOPLASMS; ORIGIN; PATIENTS; RECEPTORS
- Descriptors DEC
- ANDROSTANES; BODY; DISEASES; GLANDS; HORMONES; MATHEMATICS; MEMBRANE PROTEINS; ORGANIC COMPOUNDS; ORGANS; PROTEINS; STATISTICS; STEROID HORMONES; STEROIDS
Optional Information
- Copyright
- Copyright (c) 2014 by the authors
- Notes
- PMCID: PMC4190544; PMID: 24978437; PUBLISHER-ID: cancers-06-01351; OAI: oai:pubmedcentral.nih.gov:4190544; licensee MDPI, Basel, Switzerland.; This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).