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PMID: 22119938 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A CD44⁻/CD24⁺ phenotype is a poor prognostic marker in early invasive breast cancer.

Breast cancer research and treatment ·Vol. 133 ·No. 3 ·2012-06-00 ·Pages 979-95

Ahmed MA, Aleskandarany MA, Rakha EA, Moustafa RZ, Benhasouna A, Nolan C, Green AR, Ilyas M, Ellis IO

Abstract

A CD44(-)/CD24(+) phenotype is a poor prognostic marker in early invasive breast cancer. Breast cancer cells with high CD44 and low or absent CD24 (i.e. CD44(+)CD24(-)/low phenotype) are reported to have stem cell features. However, the clinical impact of CD24 and CD44 expression in tumours remains unclear. To explore the immunohistochemical expression of CD44 and CD24 (individually and combined) and their clinical value as prognostic and predictive markers. Immunohistochemical expression of CD24 and CD44 was studied in a large series of early primary invasive breast cancer tumours (n = 1036) prepared as a tissue microarray. Associations between the expression of each marker individually and in combination and clinico-pathological, molecular variables and patients' outcome were investigated. CD24 cytoplasmic expression was significantly associated with poor prognostic variables including high tumour grade, ER-, PR-, HER2(+), p53+ and triple negative (TN) phenotype; P < 0.05. However, CD24 expression was not significantly associated with patients' outcome. Conversely, CD44 expression was associated with favourable prognostic criteria including lower Nottingham prognostic index, ER+, HER2- and luminal phenotype; P < 0.05. Moreover, CD44 expression was found to be an independent predictor of good prognosis. In combination, the CD44(+)/CD24(-) phenotype was associated with the most favourable outcome (84 and 80% 10 year breast cancer survival [BCSS] and metastasis free survival [MFS], respectively). Contrasting this, the CD44(-)/CD24(+) phenotype was associated with the most dismal outcome (62 and 60% 10 years BCSS and MFS, respectively). CD24 and CD44 expression can individually yield prognostic data in breast cancer, but importantly, when both markers are considered; the CD44(+)/CD24(-) phenotype had the best prognosis, while the CD44(-)/CD24(+) phenotype had the worst prognosis. This shows that the relationship between basic cell biology and clinical behaviour is not always straightforward and warrants further investigations of the true clinical impact of breast cancer stem cells.

MeSH Terms
Adult Aged Biomarkers, Tumor/genetics,metabolism Breast Neoplasms/metabolism,mortality,pathology CD24 Antigen/genetics,metabolism Female Gene Expression Regulation, Neoplastic Humans Hyaluronan Receptors/genetics,metabolism Middle Aged Neoplasm Staging Prognosis Survival Analysis
Chemicals
Biomarkers, Tumor CD24 Antigen Hyaluronan Receptors
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Ahmed Mohamed A H
Division of Pathology, School of Molecular Medical Sciences, University of Nottingham, Nottingham, UK.
Aleskandarany Mohammed A
Rakha Emad A
Moustafa Radwa Z A
Benhasouna Ahmed
Nolan Christopher
Green Andrew R
Ilyas Mohammad
Ellis Ian O
Article Info
Journal
Breast cancer research and treatment
Abbr.
Breast Cancer Res Treat
ISSN
1573-7217
Published
2012-06-00
Epub
2011-00-27
Pages
979-95
Language
English
Region
Netherlands
NLM ID
8111104
Subset
IM
Grants
Medical Research Council · MC_G0900866 · United Kingdom
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