Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, Largo Professor Abel Salazar, 2, 4099-003 Porto, Portugal.
Vet J. 2011 Dec;190(3):396-402. doi: 10.1016/j.tvjl.2010.12.003. Epub 2011 Jan 26.
Canine mammary tumours (CMTs) are a very heterogeneous group of neoplasms with variable prognosis. Their aggressiveness is mainly due to their ability to invade locally and to metastasize. The degradation of extracellular matrix components is an important determinant of the invasive phenotype. The aims of this study were to analyse by immunohistochemistry and double immunofluorescence the expression of metalloproteinase 2 (MMP-2) and tissue inhibitor of metalloproteinase 2 (TIMP-2) in eight normal canine mammary glands and 118 CMTs (24 benign, 94 malignant) and to investigate relationships with metastatic disease and survival. MMP-2 and TIMP-2 expression was higher in malignant tumours than in normal canine mammary tissue and benign tumours. The main difference between benign and malignant CMTs was the pattern of expression of both molecules: benign tumours presented TIMP-2 and MMP-2 immunoreactivity in the myoepithelial cells lining the basement membrane of tubuloalveolar structures, while malignant tumours showed mainly diffuse expression in neoplastic cells. In malignant tumours, increased TIMP-2 expression was significantly associated with the development of distant metastases, lower overall survival and lower disease-free survival. MMP-2 expression was not significantly associated to any of these parameters. These results suggest that the immunohistochemical expression of TIMP-2 is a useful prognostic factor in CMTs.
犬乳腺肿瘤(CMTs)是一组具有不同预后的非常异质性肿瘤。其侵袭性主要归因于其局部侵袭和转移的能力。细胞外基质成分的降解是侵袭表型的重要决定因素。本研究的目的是通过免疫组织化学和双重免疫荧光分析 8 只正常犬乳腺组织和 118 例 CMTs(24 例良性,94 例恶性)中基质金属蛋白酶 2(MMP-2)和金属蛋白酶组织抑制剂 2(TIMP-2)的表达,并探讨其与转移性疾病和生存的关系。MMP-2 和 TIMP-2 的表达在恶性肿瘤中高于正常犬乳腺组织和良性肿瘤。良性和恶性 CMTs 之间的主要区别在于这两种分子的表达模式:良性肿瘤中,TIMP-2 和 MMP-2 免疫反应性存在于管状肺泡结构基底膜的肌上皮细胞中,而恶性肿瘤中主要在肿瘤细胞中呈现弥漫性表达。在恶性肿瘤中,TIMP-2 表达的增加与远处转移的发生、总生存率和无病生存率降低显著相关。MMP-2 的表达与这些参数均无显著相关性。这些结果表明,TIMP-2 的免疫组织化学表达是 CMTs 的一个有用的预后因素。