EGFR and microvessel density in canine malignant mammary tumours

被引:51
作者
Carvalho, Maria Isabel [1 ]
Guimaraes, Maria Joao [2 ]
Pires, Isabel [3 ]
Prada, Justina [3 ]
Silva-Carvalho, Ricardo [4 ,5 ]
Lopes, Carlos [2 ]
Queiroga, Felisbina L. [1 ,6 ]
机构
[1] Univ Tras Os Montes & Alto Douro, Dept Vet Sci, P-5001801 Vila Real, Portugal
[2] Univ Porto, Inst Ciencias Biomed Abel Salazar, P-4099003 Oporto, Portugal
[3] Univ Tras Os Montes & Alto Douro, Dept Vet Sci, CECAV, P-5001801 Vila Real, Portugal
[4] Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, Braga, Portugal
[5] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
[6] Univ Porto, CECA, P-4099003 Oporto, Portugal
关键词
EGFR; Angiogenesis; MVD; CD31; Canine mammary tumours; EPIDERMAL-GROWTH-FACTOR; FACTOR RECEPTOR EGFR; TYROSINE KINASE INHIBITORS; CLINICAL-SIGNIFICANCE; MASITINIB MESYLATE; ESTROGEN-RECEPTOR; COX-2; EXPRESSION; BREAST-CANCER; ANGIOGENESIS; CARCINOMAS;
D O I
10.1016/j.rvsc.2013.09.003
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The epidermal growth factor receptor (EGFR) is a transmembrane tyrosine kinase receptor which has been shown to have an important role in human breast cancer. Its role appears to be associated with increased angiogenesis and metastasis. In order to clarify its role in canine mammary tumours (CMT), 61 malignant neoplasms were studied by using immunohistochemistry, comparing expression of EGFR, microvessel density (MVD) by CD31 immunolabelling and characteristics of tumour aggressiveness. High EGFR immunoexpression was statistically significantly associated with tumour size, tumour necrosis, mitotic grade, histological grade of malignancy and clinical stage. High CD31 immunoreactivity was statistically significantly associated with tubule formation, histological grade of malignancy and clinical stage. A positive correlation between EGFR and CD31 immunoexpression (r = 0.843; P < 0.001) was also observed. Results suggest that an over-expression of EGFR may contribute to increased angiogenesis and aggression in malignant CMT, presenting the possibility of using EGFR inhibitors in the context of metastatic disease treatment. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1094 / 1099
页数:6
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