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CD24 expression is specific for tamoxifen-resistant ductal breast cancer cases.
- Source :
-
Anticancer research [Anticancer Res] 2006 Jan-Feb; Vol. 26 (1B), pp. 629-34. - Publication Year :
- 2006
-
Abstract
- Background: In breast cancer, the expression of CD24 represents a poorly recognised unfavourable prognostic factor. CD24 has been described to be potentially down-regulated by estrogen receptor alpha (ER). The present study was aimed at examining the predictive value of CD24 expression in tamoxifen-treated breast cancer cases.<br />Materials and Methods: Sixty patients with primary invasive ductal breast cancers with post-operative tamoxifen treatment were enrolled in the study. Immmunohistochemical reactions were performed using monoclonal antibodies directed against CD24 and ER.<br />Results: Cases demonstrating cytoplasmic-membranous expression of CD24 (CD24c-m) proved to be characterised by a significantly lower expression of ER as compared to CD24c-m-negative cases. A multivariate progression analysis based on the Cox proportional hazard model demonstrated that CD24c-m expression is an independent prognostic factor for poor overall survival.<br />Conclusion: The data from the present study suggested that CD24c-m expression is specific for tamoxifen-resistant breast cancer cases. CD24 should be subjected to comprehensive studies as a marker of resistance to tamoxifen treatment.
- Subjects :
- Biomarkers, Tumor biosynthesis
Breast Neoplasms pathology
Carcinoma, Ductal, Breast pathology
Drug Resistance, Neoplasm
Female
Humans
Immunohistochemistry
Middle Aged
Predictive Value of Tests
Receptors, Estrogen biosynthesis
Antineoplastic Agents, Hormonal pharmacology
Breast Neoplasms drug therapy
Breast Neoplasms metabolism
CD24 Antigen biosynthesis
Carcinoma, Ductal, Breast drug therapy
Carcinoma, Ductal, Breast metabolism
Tamoxifen pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0250-7005
- Volume :
- 26
- Issue :
- 1B
- Database :
- MEDLINE
- Journal :
- Anticancer research
- Publication Type :
- Academic Journal
- Accession number :
- 16739331