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基质金属蛋白酶及其抑制剂在非小细胞肺癌中的差异表达

Differential expression of matrix metalloproteinases and their inhibitors in non-small cell lung cancer.

作者信息

Thomas P, Khokha R, Shepherd F A, Feld R, Tsao M S

机构信息

Service d'Oncologie Respiratoire, Departement des Maladies Respiratoires, Hopital Ste-Marguerite, 270 Bd Ste Marguerite, 13009 Marseille, France.

出版信息

J Pathol. 2000 Feb;190(2):150-6. doi: 10.1002/(SICI)1096-9896(200002)190:2<150::AID-PATH510>3.0.CO;2-W.

Abstract

In a comprehensive immunohistochemical study of the expression of ten metalloproteinases (MMPs) and their four inhibitors (TIMPs) in 115 non-small cell lung carcinomas (NSCLCs), the findings have been correlated with the histological and clinical features of the tumours. All MMPs and TIMPs were expressed in tumours, with frequencies ranging from 41% for MMP-2 to 68% for MMP-13. Stromal immunoreactivity ranged from 6% for TIMP-4 to 87% for MMP-13. In some tumours, an overexpression of these proteins, as revealed by stronger staining in cancer cells than in adjacent normal bronchial epithelium, was also observed. The frequency ranged from 1% for MMP-3 to 28% for MMP-13. Compared with squamous cell carcinoma (SqCC), adenocarcinoma (AdC) more frequently overexpressed MMP-1, -11, -13, -14, and TIMP-2, and TIMP-1 and/or TIMP-2 overexpression positively correlated with more advanced stage disease. None of the MMP or TIMP expression correlated with the ras genotype of the tumours. The higher frequency of MMP overexpression in AdC than in SqCC may relate to the greater tendency of the former for systemic metastasis. The association of TIMP-1 overexpression with more advanced disease may suggest a role in prognosis.

摘要

在一项针对115例非小细胞肺癌(NSCLC)中十种金属蛋白酶(MMPs)及其四种抑制剂(TIMPs)表达的全面免疫组织化学研究中,研究结果已与肿瘤的组织学和临床特征相关联。所有MMPs和TIMPs在肿瘤中均有表达,表达频率从MMP-2的41%到MMP-13的68%不等。基质免疫反应性从TIMP-4的6%到MMP-13的87%不等。在一些肿瘤中,还观察到这些蛋白的过表达,表现为癌细胞中的染色比相邻正常支气管上皮更强。频率范围从MMP-3的1%到MMP-13的28%。与鳞状细胞癌(SqCC)相比,腺癌(AdC)更频繁地过表达MMP-1、-11、-13、-14和TIMP-2,并且TIMP-1和/或TIMP-2过表达与更晚期疾病呈正相关。MMP或TIMP的表达与肿瘤的ras基因型均无相关性。AdC中MMP过表达的频率高于SqCC,这可能与前者更易发生全身转移的倾向有关。TIMP-1过表达与更晚期疾病的关联可能提示其在预后中的作用。

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