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PMID: 21680574 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Breast cancer stem cell markers CD44, CD24 and ALDH1: expression distribution within intrinsic molecular subtype.

Journal of clinical pathology ·Vol. 64 ·No. 11 ·2011-11-00 ·Pages 937-46

Ricardo S, Vieira AF, Gerhard R, Leitão D, Pinto R, Cameselle-Teijeiro JF, Milanezi F, Schmitt F, Paredes J

Abstract

The study of CD44/CD24 and ALDH1 expression is the most accurate method to identify cancer stem cells (CSC) from breast cancer populations. However, the overlap between CD44(+)CD24(-/low) and ALDH1(high) CSC phenotypes in breast cancer seems to be very small, as well as their distribution among intrinsic breast cancer subtypes. Due to this discrepancy, it is imperative to improve the understanding of breast CSC marker distribution. 466 invasive breast carcinomas and eight breast cancer cell lines were analysed for the expression of CD44, CD24 and ALDH1, to evaluate their distribution among the distinct molecular subtypes. Basal-like tumours (76.5%) contained the higher percentage of cells with the CSC phenotype CD44(+)CD24(-/low) (p<0.0001). From ALDH1-positive cases, 39.4% were also basal-like tumours (p<0.0001). The analysis of breast cancer cell lines indicated that luminal cell lines are mainly enriched in a CD44(-/low)CD24(+) cell population, basal/mesenchymal breast cancer cell lines are enriched in the CD44(+)CD24(-/low) phenotype, whereas the remaining basal/epithelial cell lines are mainly positive for both markers. ALDH1 activity was mainly found in HER-OE and basal/epithelial breast cancer cell. CD44(+)CD24(-/low) and ALDH1(+) phenotypes seem to identify CSC with distinct levels of differentiation. It seems that the paramount method and biomarkers that identify breast CSC within the distinct molecular subtypes need to be better explored, because it is pivotal to translate the CSC concept to clinical practice. In the future, the recognition of reliable markers to distinguish the CSC pool in each molecular subtype will be decisive for the development of specific target therapies.

MeSH Terms
Adult Aged Aged, 80 and over Aldehyde Dehydrogenase 1 Family Biomarkers, Tumor/metabolism Breast Neoplasms/metabolism,mortality,pathology CD24 Antigen/metabolism Cell Line, Tumor Disease-Free Survival Female Humans Hyaluronan Receptors/metabolism Immunohistochemistry Isoenzymes/metabolism Kaplan-Meier Estimate Middle Aged Neoplastic Stem Cells/metabolism,pathology Phenotype Retinal Dehydrogenase/metabolism
Chemicals
Biomarkers, Tumor CD24 Antigen Hyaluronan Receptors Isoenzymes Aldehyde Dehydrogenase 1 Family ALDH1A1 protein, human Retinal Dehydrogenase
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Ricardo Sara
IPATIMUP-Institute of Molecular Pathology and Immunology of Porto University, Porto, Portugal.
Vieira André Filipe
Gerhard Renê
Leitão Dina
Pinto Regina
Cameselle-Teijeiro Jorge F
Milanezi Fernanda
Schmitt Fernando
Paredes Joana
Article Info
Journal
Journal of clinical pathology
Abbr.
J Clin Pathol
ISSN
1472-4146
Published
2011-11-00
Epub
2011-00-16
Pages
937-46
Language
English
Region
England
NLM ID
0376601
Subset
IM
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