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Glut-1 Expression Correlates with Basal-like Breast Cancer

Authors :
Sudeshna Bandyopadhyay
Quratulain Ahmed
Rouba Ali-Fehmi
Bassam Albashiti
Yaser R. Hussein
Assaad Semaan
Zeina Nahleh
Tarek Jazaerly
Source :
Translational Oncology. 4(6):321-327
Publication Year :
2011
Publisher :
Elsevier BV, 2011.

Abstract

INTRODUCTION: Glucose transporter 1 (Glut-1) is a facilitative glucose transporter expressed in many cancers including breast cancer. Basal-like breast cancer (BLBC) is a high-risk disease associated with poor prognosis and lacks the benefit of targeted therapy. The aim of this study was to characterize the immunohistochemical (IHC) expression of Glut-1 in patients with BLBC compared with non-BLBC. MATERIALS AND METHODS: We identified 523 cases of invasive breast carcinoma from our database. The clinicopathologic findings and the biologic markers including estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (Her2) status were reviewed. IHC stains for cytokeratin 5/6 (CK5/6), epidermal growth factor receptor (EGFR), p53, and Glut-1 were performed on tissue microarray using standard procedures. BLBC was defined as ER-,PR-, Her2-, and CK5/6+ and/or EGFR+. RESULTS: Of informative cases, 14.7% were categorized as BLBC versus 85.3% as non-BLBC. Glut-1 was expressed in 42 (76.4%) of 55 BLBCs, whereas only 55 (23.8%) of 231 non-BLBCs showed immunostaining for Glut-1 (P < .001). Overall, Glut-1 expression was significantly associated with high histologic grade, ER negativity, PR negativity, CK5/6 positivity, EGFR expression, and high p53 expression (P < .001). However, there was no correlation between Glut-1 immunostaining and patient's outcome. CONCLUSIONS: Our results show that Glut-1 is significantly associated with BLBC and might be a potential therapeutic target for this aggressive subgroup of breast cancer, and this warrants further investigations.

Details

ISSN :
19365233
Volume :
4
Issue :
6
Database :
OpenAIRE
Journal :
Translational Oncology
Accession number :
edsair.doi.dedup.....2401c0085708f39d1204b8dfb4a81a8b
Full Text :
https://doi.org/10.1593/tlo.11256