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Role of matrix metalloproteinases in invasion, and metastasis: biology, diagnosis and inhibitors

机译:基质金属蛋白酶在侵袭和转移中的作用:生物学,诊断和抑制剂

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摘要

The processes of tumor invasion and subsequent metastasis are the most lethal, aspects of cancer. Whilst many factors are involved, the matrix metalloproteinases (MMPs) have been implicated as key-rate limiting enzymes in the invasive process. This family consisting of eight members of similar structure, can be roughly divided into three groups based on substrate specificity. All are secreted in a latent form and require proteolytic cleavage for activation. The expression of these enzymes is regulated at the transcriptional level by a variety of growth factors and oncogenes. They are also regulated at the protein level by a family of specific inhibitors called the tissue inhibitors of metalloproteinases (TIMPs). Studies, in human tumour samples have shown a positive correlation between metalloproteinase expression and metastatic potential. The levels of metalloproteinase expression, have been manipulated using molecular biology techniques in several cell lines and shown a similar correlation. These results suggest that an understanding of metalloproteinase expression and proteolytic activity may lead to the development of effective therapeutic agents with the potential, to reduce the incidence of metastatic cancer.
机译:肿瘤入侵和随后转移的过程是癌症中最致命的方面。尽管涉及许多因素,但基质金属蛋白酶(MMP)已被认为是侵入过程中的关键速率限制酶。该家族由八个具有相似结构的成员组成,可以根据底物特异性大致分为三类。全部以潜伏形式分泌,需要蛋白水解裂解才能激活。这些酶的表达在转录水平上受多种生长因子和癌基因的调控。它们也被称为金属蛋白酶组织抑制剂(TIMPs)的一系列特异性抑制剂在蛋白质水平上调节。在人类肿瘤样本中的研究表明,金属蛋白酶表达与转移潜力之间存在正相关。金属蛋白酶的表达水平已使用分子生物学技术在几种细胞系中进行了操纵,并显示出相似的相关性。这些结果表明,对金属蛋白酶表达和蛋白水解活性的了解可能导致开发具有潜力的有效治疗剂,以减少转移性癌症的发生。

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