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

被引:481
作者
Ricardo, Sara [1 ,2 ,3 ]
Vieira, Andre Filipe [1 ,2 ]
Gerhard, Rene [1 ]
Leitao, Dina [1 ,4 ]
Pinto, Regina [1 ]
Cameselle-Teijeiro, Jorge F. [5 ]
Milanezi, Fernanda [1 ]
Schmitt, Fernando [1 ,4 ]
Paredes, Joana [1 ,4 ]
机构
[1] Univ Porto, IPATIMUP, Inst Mol Pathol & Immunol, P-4200465 Oporto, Portugal
[2] Abel Salazar Biomed Sci Inst, ICBAS, Oporto, Portugal
[3] Vale Polytech Hlth Inst N, Vale Sousa Higher Sch Hlth, Dept Anat Pathol Cytol & Tanatol, Gandra, Portugal
[4] Univ Porto, Fac Med, P-4200465 Oporto, Portugal
[5] CHUVI, Vigo, Spain
关键词
ALDEHYDE DEHYDROGENASE; ESTROGEN-RECEPTOR; CARCINOMA; IDENTIFICATION; PHENOTYPE; PROGNOSIS; LINES; CD44(+)/CD24(-/LOW); HETEROGENEITY; RESISTANCE;
D O I
10.1136/jcp.2011.090456
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
Background and Aim 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. Methods 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. Results 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. Conclusions 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.
引用
收藏
页码:937 / 946
页数:10
相关论文
共 59 条
[1]
Abraham BK, 2005, CLIN CANCER RES, V11, P1154
[2]
Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[3]
Reduction of CD44+/CD24- breast cancer cells by conventional cytotoxic chemotherapy [J].
Aulmann, Sebastian ;
Waldburger, Nina ;
Penzel, Roland ;
Andrulis, Mindaugas ;
Schirmacher, Peter ;
Sinn, Hans Peter .
HUMAN PATHOLOGY, 2010, 41 (04) :574-581
[4]
Tissue microarray: A simple technology that has revolutionized research in pathology [J].
Avninder, S. ;
Ylaya, K. ;
Hewitt, S. M. .
JOURNAL OF POSTGRADUATE MEDICINE, 2008, 54 (02) :158-162
[5]
Tissue-specific promoters active in CD44+CD24-/low breast cancer cells [J].
Bauerschmitz, Gerd J. ;
Ranki, Tuuli ;
Kangasniemi, Lotta ;
Ribacka, Camilla ;
Eriksson, Minna ;
Porten, Marius ;
Herrmann, Isabell ;
Ristimaki, Ari ;
Virkkunen, Pekka ;
Tarkkanen, Maija ;
Hakkarainen, Tania ;
Kanerva, Anna ;
Rein, Daniel ;
Pesonen, Sari ;
Hemminki, Akseli .
CANCER RESEARCH, 2008, 68 (14) :5533-5539
[6]
CD24 expression in ductal carcinoma in situ and invasive ductal carcinoma of breast: An immunohistochemistry-based pilot study [J].
Bircan, Sema ;
Kapucuoglu, Nilgun ;
Baspinar, Sirin ;
Inan, Gulsun ;
Candir, Ozden .
PATHOLOGY RESEARCH AND PRACTICE, 2006, 202 (08) :569-576
[7]
Cell type-specific DNA methylation patterns in the human breast [J].
Bloushtain-Qimron, Noga ;
Yao, Jun ;
Snyder, Eric L. ;
Shipitsin, Michail ;
Campbell, Lauren L. ;
Mani, Sendurai A. ;
Hua, Min ;
Chen, Haiyan ;
Ustyansky, Vadim ;
Antosiewicz, Jessica E. ;
Argani, Pedram ;
Halushka, Marc K. ;
Thomson, James A. ;
Pharoah, Paul ;
Porgador, Angel ;
Sukumar, Saraswati ;
Parsons, Ramon ;
Richardson, Andrea L. ;
Stampfer, Martha R. ;
Gelman, Rebecca S. ;
Nikolskaya, Tatiana ;
Nikolsky, Yuri ;
Polyak, Kornelia .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (37) :14076-14081
[8]
Tumor-Endothelial Interaction Links the CD44+/CD24- Phenotype with Poor Prognosis in Early-Stage Breast Cancer [J].
Buess, Martin ;
Rajski, Michal ;
Vogel-Durrer, Brigitte M. L. ;
Herrmann, Richard ;
Rochlitz, Christoph .
NEOPLASIA, 2009, 11 (10) :987-1002
[9]
Gene expression profiling of breast cell lines identifies potential new basal markers [J].
Charafe-Jauffret, E ;
Ginestier, C ;
Monville, F ;
Finetti, P ;
Adélaïde, J ;
Cervera, N ;
Fekairi, S ;
Xerri, L ;
Jacquemier, J ;
Birnbaum, D ;
Bertucci, F .
ONCOGENE, 2006, 25 (15) :2273-2284
[10]
Cancer stem cells in breast: Current opinion and future challenges [J].
Charafe-Jauffret, Emmanuelle ;
Monville, Florence ;
Ginestier, Christophe ;
Dontu, Gabriela ;
Birnbaum, Daniel ;
Wicha, Max S. .
PATHOBIOLOGY, 2008, 75 (02) :75-84