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Glut-1 Expression Correlates with Basal-like Breast Cancer
Yaser R Hussein1, Sudeshna Bandyopadhyay, Assaad Semaan
1Department of Pathology, Wayne State University School of Medicine, Detroit, MI, USA.
Translational Oncology
|December 23, 2011
Summary
Glucose transporter 1 (Glut-1) is highly expressed in basal-like breast cancer (BLBC), a high-risk subtype. This finding suggests Glut-1 may be a potential therapeutic target for BLBC patients.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Glucose transporter 1 (Glut-1) is a key protein in glucose metabolism.
- Basal-like breast cancer (BLBC) is an aggressive subtype with poor prognosis and limited targeted therapies.
- Understanding Glut-1 expression in BLBC is crucial for identifying new treatment strategies.
Purpose of the Study:
- To investigate the immunohistochemical (IHC) expression of Glut-1 in BLBC.
- To compare Glut-1 expression between BLBC and non-BLBC subtypes.
- To explore the association of Glut-1 expression with clinicopathologic features in breast cancer.
Main Methods:
- Retrospective analysis of 523 invasive breast carcinoma cases.
- Immunohistochemical (IHC) staining for Glut-1, cytokeratin 5/6 (CK5/6), epidermal growth factor receptor (EGFR), and p53.
- Classification of BLBC based on estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (Her2) negativity, and CK5/6 and/or EGFR positivity.
Main Results:
- Glut-1 was significantly overexpressed in BLBC (76.4%) compared to non-BLBC (23.8%) (P < .001).
- Glut-1 expression strongly correlated with high histologic grade, ER/PR negativity, CK5/6 positivity, EGFR expression, and high p53 expression (P < .001).
- No significant correlation was found between Glut-1 immunostaining and patient outcome.
Conclusions:
- Glut-1 is significantly associated with the basal-like breast cancer subtype.
- Glut-1 represents a potential therapeutic target for aggressive BLBC.
- Further research is warranted to explore Glut-1-targeted therapies for BLBC.
