Epithelial Cell Adhesion Molecule Expression in Canine Tumours

被引:5
作者
Thamm, D. H. [1 ,2 ,4 ]
Hayes, D. F. [5 ]
Meuten, T. [1 ,3 ]
Laver, T.
Thomas, D. G. [5 ]
机构
[1] Colorado State Univ, Coll Vet Med & Biomed Sci, Dept Clin Sci, Ft Collins, CO 80523 USA
[2] Colorado State Univ, Coll Vet Med & Biomed Sci, Cell & Mol Biol Grad Program, Ft Collins, CO 80523 USA
[3] Colorado State Univ, Coll Vet Med & Biomed Sci, Dept Microbiol Immunol & Pathol, Ft Collins, CO 80523 USA
[4] Univ Colorado, Ctr Comprehens Canc, 1665 N Ursula St, Aurora, CO 80045 USA
[5] Univ Michigan, Ctr Comprehens Canc, 1500 E Med Ctr Dr SPC 5942, Ann Arbor, MI 48109 USA
关键词
carcinoma; dog; epithelial cell adhesion molecule; immunohistochemistry; EP-CAM; EPCAM EXPRESSION; BREAST-CANCER; PROGNOSIS; OVEREXPRESSION; CARCINOMAS; LINE;
D O I
10.1016/j.jcpa.2016.07.010
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Epithelial cell adhesion molecule (EpCAM) is expressed in most human normal and neoplastic tissues of epithelial derivation and may have an association with tumour cell aggressiveness, a stem cell-like phenotype and clinical outcome. Antibody-based strategies for the targeting and capture of EpCAM-expressing tumour cells are showing promise, both as diagnostic tools and potential therapies. The aim of this study was to assess EpCAM expression in canine tumours. EpCAM expression was assessed in tumour cell lines via gene expression profiling and in formalin-fixed and paraffin wax-embedded tissues from canine carcinomas representing various anatomical sites by immunohistochemistry. EpCAM mRNA expression was higher in cell lines from carcinomas than those derived from sarcomas or haemopoietic tumours. EpCAM was expressed by >2/3 of tumour cells in 71% of canine carcinomas evaluated, irrespective of histotype, with the exception of carcinomas of the adrenal gland. Canine sarcomas and haemopoietic tumours were uniformly negative. Most canine carcinomas express EpCAM and so could be suitable for the study of EpCAM-directed diagnostics and therapeutics. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:299 / 304
页数:6
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