基质金属蛋白酶在恶性间皮瘤中的潜在作用

Shibo Ying, Yanbin Wang, Lyuyang Lyu
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引用次数: 1

摘要

恶性间皮瘤(MM)是一种罕见的、侵袭性的、高致死率的癌症,主要由接触石棉纤维引起。基质金属蛋白酶(MMPs)是一个锌依赖的内多肽酶家族,参与转移,其过表达与肿瘤细胞侵袭和转移相关,因为它们降解细胞外基质(ECM)并处理粘附和细胞骨架蛋白、生长因子、趋化因子和细胞因子。最近的证据表明MMPs参与MM的进展,表明它们是潜在的新型生物标志物和癌症治疗的有吸引力的靶点。在本章中,我们将根据体内和体外实验证据描述MMPs的致癌机制,概述临床发现,并推测MMPs在MM中的可能作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential Roles of Matrix Metalloproteinases in Malignant Mesothelioma
Malignant mesothelioma (MM) is a rare, aggressive, and highly lethal cancer that is primary induced by exposure to asbestos fibers. Matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases that are involved in metastasis, and their overexpression correlates with tumor cell invasion and metastasis because they degrade the extracellular matrix (ECM) and process adhesion and cytoskeletal proteins, growth factors, chemokines, and cytokines. Recent evidence has shown that MMPs participate in MM progression, indicating that they are potential novel biomarkers and attractive targets for cancer therapy. In this chapter, we will describe MMPs in carcinogenic mechanisms based on in vivo and in vitro experimental evidence, outline the clinical findings, and speculate the possible roles of MMPs in MM.
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