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胶原酶-3在恶性肿瘤中的表达概述及其作为抗肿瘤治疗靶点的潜在价值分析。

An overview of collagenase-3 expression in malignant tumors and analysis of its potential value as a target in antitumor therapies.

作者信息

Pendás A M, Uría J A, Jiménez M G, Balbín M, Freije J P, López-Otín C

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Universidad de Oviedo, 33006, Oviedo, Spain.

出版信息

Clin Chim Acta. 2000 Feb 15;291(2):137-55. doi: 10.1016/s0009-8981(99)00225-9.

DOI:10.1016/s0009-8981(99)00225-9
PMID:10675720
Abstract

Collagenase-3 (MMP-13) is a member of the matrix metalloproteinase family of endopeptidases that is characterized by a potent degrading activity against a wide spectrum of substrates. This enzyme was first detected in breast carcinomas but it is also overexpressed in a variety of malignant tumors including head and neck carcinomas, chondrosarcomas, skin carcinomas, and carcinomas of the female genital tract. Clinical studies have revealed that in all these tumors collagenase-3 expression is associated with invasive and metastatic tumors. Analysis of the molecular mechanisms underlying its marked overexpression in malignant tumors has allowed to identify different cytokines, growth factors and tumor promoters with ability to up-regulate collagenase-3 expression in tumor cells, or in stromal fibroblasts surrounding epithelial tumor cells. The first strategies designed to target this enzyme are being developed, and are mainly directed to prepare synthetic inhibitors with ability to selectively block the collagenase-3 proteolytic activity. Alternatively, inhibitors of the signal transduction pathways mediating the expression of this enzyme by tumor cells may also be useful for collagenase-3 targeting. These studies together with those performed on other enzymes associated with tumor processes may lead to the development of novel therapeutic strategies to control the progression and metastatic capacity of neoplastic cells.

摘要

胶原酶-3(MMP-13)是一种内肽酶基质金属蛋白酶家族的成员,其特点是对多种底物具有强大的降解活性。这种酶最初在乳腺癌中被检测到,但在包括头颈癌、软骨肉瘤、皮肤癌和女性生殖道癌在内的多种恶性肿瘤中也过度表达。临床研究表明,在所有这些肿瘤中,胶原酶-3的表达与侵袭性和转移性肿瘤相关。对其在恶性肿瘤中显著过度表达的分子机制进行分析,已确定了不同的细胞因子、生长因子和肿瘤启动子,它们能够上调肿瘤细胞或上皮肿瘤细胞周围基质成纤维细胞中胶原酶-3的表达。针对这种酶的首批策略正在研发中,主要致力于制备能够选择性阻断胶原酶-3蛋白水解活性的合成抑制剂。或者,介导肿瘤细胞表达这种酶的信号转导途径的抑制剂也可能对靶向胶原酶-3有用。这些研究以及对与肿瘤进程相关的其他酶所进行的研究,可能会促成新型治疗策略的开发,以控制肿瘤细胞的进展和转移能力。

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