Claudin-Low Breast Cancer; Clinical & Pathological Characteristics

被引:116
作者
Dias, Kay [1 ,2 ]
Dvorkin-Gheva, Anna [3 ]
Hallett, Robin M. [3 ]
Wu, Ying [2 ]
Hassell, John [1 ,3 ]
Pond, Gregory R. [2 ]
Levine, Mark
Whelan, Tim [2 ]
Bane, Anita L. [1 ,2 ]
机构
[1] McMaster Univ, Dept Pathol & Mol Med, Hamilton, ON, Canada
[2] McMaster Univ, Dept Oncol, Hamilton, ON, Canada
[3] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON, Canada
基金
加拿大健康研究院;
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; TUMOR-INITIATING CELLS; STEM-CELLS; EXPRESSION; IDENTIFICATION; RECEPTOR; SUBTYPE; IMMUNOHISTOCHEMISTRY; PREDICTOR; SIGNATURE;
D O I
10.1371/journal.pone.0168669
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Claudin-low breast cancer is a molecular type of breast cancer originally identified by gene expression profiling and reportedly associated with poor survival. Claudin-low tumors have been recognised to preferentially display a triple-negative phenotype, however only a minority of triple-negative breast cancers are claudin-low. We sought to identify an immunohistochemical profile for claudin-low tumors that could facilitate their identification in formalin fixed paraffin embedded tumor material. First, an in silico collection of similar to 1600 human breast cancer expression profiles was assembled and all claudin-low tumors identified. Second, genes differentially expressed between claudin-low tumors and all other molecular subtypes of breast cancer were identified. Third, a number of these top differentially expressed genes were tested using immunohistochemistry for expression in a diverse panel of breast cancer cell lines to determine their specificity for claudin-low tumors. Finally, the immunohistochemical panel found to be most characteristic of claudin-low tumors was examined in a cohort of 942 formalin fixed paraffin embedded human breast cancers with > 10 years clinical followup to evaluate the clinico-pathologic and survival characteristics of this tumor subtype. Using this approach we determined that claudin-low breast cancer is typically negative for ER, PR, HER2, claudin 3, claudin 4, claudin 7 and E-cadherin. Claudin-low tumors identified with this immunohistochemical panel, were associated with young age of onset, higher tumor grade, larger tumor size, extensive lymphocytic infiltrate and a circumscribed tumor margin. Patients with claudin-low tumors had a worse overall survival when compared to patients with luminal A type breast cancer. Interestingly, claudin-low tumors were associated with a low local recurrence rate following breast conserving therapy. In conclusion, a limited panel of antibodies can facilitate the identification of claudin-low tumors. Furthermore, claudin-low tumors identified in this manner display similar clinical, pathologic and survival characteristics to claudin-low tumors identified from fresh frozen tumor material using gene expression profiling.
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页数:17
相关论文
共 44 条
[1]   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
[2]  
Allred DC, 1998, MODERN PATHOL, V11, P155
[3]   Concurrent adjuvant systemic therapy and accelerated radiotherapy in triple-negative breast cancer: A feasibility trial. [J].
Ashworth, Rene Eleanor ;
Adams, Sylvia ;
Fenton-Kerimian, Maria ;
Sacris, Erlinda ;
Speyer, James L. ;
Leichman, Cynthia G. ;
Janosky, Maxwell Dale ;
Guo, Songchuan ;
Goldberg, Judith D. ;
Novik, Yelena ;
Formenti, Sylvia .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (15)
[4]   TGFβ/TNFα-Mediated Epithelial-Mesenchymal Transition Generates Breast Cancer Stem Cells with a Claudin-Low Phenotype [J].
Asiedu, Michael K. ;
Ingle, James N. ;
Behrens, Marshall D. ;
Radisky, Derek C. ;
Knutson, Keith L. .
CANCER RESEARCH, 2011, 71 (13) :4707-4719
[5]  
Bane AL, 2014, ANN ONCOL
[6]   Clinical-pathologic significance of cancer stem cell marker expression in familial breast cancers [J].
Bane, Anita ;
Viloria-Petit, Alicia ;
Pinnaduwage, Dushanthi ;
Mulligan, Anna Marie ;
O'Malley, Frances P. ;
Andrulis, Irene L. .
BREAST CANCER RESEARCH AND TREATMENT, 2013, 140 (01) :195-205
[7]   Adjustment of systematic microarray data biases [J].
Benito, M ;
Parker, J ;
Du, Q ;
Wu, JY ;
Xang, D ;
Perou, CM ;
Marron, JS .
BIOINFORMATICS, 2004, 20 (01) :105-114
[8]  
Benjamini Y, 2001, ANN STAT, V29, P1165
[9]   TGFβ induces the formation of tumour-initiating cells in claudinlow breast cancer [J].
Bruna, Alejandra ;
Greenwood, Wendy ;
Le Quesne, John ;
Teschendorff, Andrew ;
Miranda-Saavedra, Diego ;
Rueda, Oscar M. ;
Sandoval, Jose L. ;
Vidakovic, Ana Tufegdzic ;
Saadi, Amel ;
Pharoah, Paul ;
Stingl, John ;
Caldas, Carlos .
NATURE COMMUNICATIONS, 2012, 3
[10]   Aldehyde Dehydrogenase 1-Positive Cancer Stem Cells Mediate Metastasis and Poor Clinical Outcome in Inflammatory Breast Cancer [J].
Charafe-Jauffret, Emmanuelle ;
Ginestier, Christophe ;
Iovino, Flora ;
Tarpin, Carole ;
Diebel, Mark ;
Esterni, Benjamin ;
Houvenaeghel, Gilles ;
Extra, Jean-Marc ;
Bertucci, Francois ;
Jacquemier, Jocelyne ;
Xerri, Luc ;
Dontu, Gabriela ;
Stassi, Giorgio ;
Xiao, Yi ;
Barsky, Sanford H. ;
Birnbaum, Daniel ;
Viens, Patrice ;
Wicha, Max S. .
CLINICAL CANCER RESEARCH, 2010, 16 (01) :45-55