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首页> 外文期刊>International Journal of Experimental Pathology >Comparative study of the expression of metalloproteases and their inhibitors in different localizations within primary tumours and in metastatic lymph nodes of breast cancer.
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Comparative study of the expression of metalloproteases and their inhibitors in different localizations within primary tumours and in metastatic lymph nodes of breast cancer.

机译:金属蛋白酶及其抑制剂在乳腺癌原发灶和转移性淋巴结内不同部位表达的比较研究。

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摘要

Studies on metastasic lesions from human carcinomas are scarce. Therefore there is a need for such studies to identify the expression of the biological factors that will help in the assessment of the natural history of breast cancer. Here an immunohistochemical study was performed using tissue arrays and specific antibodies against matrix metalloproteinases (MMPs)-1, 2, 7, 9, 11, 13, 14 and tissue inhibitors of metalloproteases (TIMPs)-1, 2 and 3 in 39 patients with breast cancer. Specimens from 39 patients with node-positive carcinomas were examined and the analysis was performed at the central core of the tumour, at the invasive front, and in the metastasic axillary lymph nodes (MALNs). Global expression of MMP-1, 7 and 14, TIMP-1, and 3, were significantly higher at the centre of the tumour compared with the invasive front or the MALNs. Significantly higher expression of MMP-7 and 14, and TIMP-3, by fibroblast-like cells and mononuclear inflammatory cells (MICs) was seen in MALNs. In addition, in the tumour centre, the expression of MMP-11 and TIMP-1 and 2 by MICs, as well as TIMP-2 expression by fibroblast-like cells, were associated significantly with the occurrence of distant metastasis. In contrast, TIMP-3 expression by tumour cells or by fibroblast-like cells in this same tumour locations, as well as TIMP-1 expression by fibroblast-like cells at the invasive front, were associated significantly with poor prognosis. However, the expression of all of these biological factors in MALNs was not associated with the development of distant metastasis. Our data suggest that there is prognostic relevance to the expression of MMPs and TIMPs in the stromal cells of primary tumours, rather than to the expression of these enzymes in MALNs.
机译:关于人类癌转移灶的研究很少。因此,需要进行这样的研究以鉴定有助于评估乳腺癌自然史的生物学因子的表达。在这里,对39例患者进行了免疫组织化学研究,方法是使用组织芯片和针对基质金属蛋白酶(MMPs)-1、2、7、9、11、13、14的特异性抗体以及金属蛋白酶组织抑制剂(TIMPs)-1、2和3。乳腺癌。检查了39例淋巴结阳性癌患者的标本,并在肿瘤的中心核心,浸润性前端和转移性腋窝淋巴结(MALN)中进行了分析。与侵袭性前沿或MALN相比,MMP-1、7和14,TIMP-1和3的整体表达在肿瘤中心明显更高。在MALNs中观察到,成纤维细胞样细胞和单核炎性细胞(MIC)显着提高了MMP-7和14和TIMP-3的表达。另外,在肿瘤中心,MICs的MMP-11和TIMP-1和2的表达以及成纤维细胞样细胞的TIMP-2的表达与远处转移的发生显着相关。相反,在相同的肿瘤位置,肿瘤细胞或成纤维细胞样细胞的TIMP-3表达以及侵袭性前沿的成纤维细胞样细胞的TIMP-1表达与不良预后显着相关。但是,所有这些生物学因素在MALNs中的表达与远处转移的发生无关。我们的数据表明,与原发性肿瘤基质细胞中MMPs和TIMPs的表达具有预后相关性,而不与MALNs中这些酶的表达有关。

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