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肿瘤转移与nm23:当前概念

Tumor metastasis and nm23: current concepts.

作者信息

Steeg P S, Cohn K H, Leone A

机构信息

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Cancer Cells. 1991 Jul;3(7):257-62.

PMID:1911039
Abstract

Reduced expression and/or somatic allelic deletion of nm23 is associated with high metastatic potential in several types of rodent tumors and human breast and colorectal carcinomas. Transfection of murine nm23-1 cDNA into highly metastatic murine K-1735 TK melanoma cells results in a reduced incidence of primary tumor formation, significant reduction in tumor metastatic potential, and altered responsiveness to the cytokine, transforming growth factor beta. Here we discuss emerging concepts concerning nm23, such as its varied pattern of alteration/expression in tumor metastasis, its effect on tumorigenesis, and its possible biochemical functions.

摘要

nm23的表达降低和/或体细胞等位基因缺失与几种啮齿动物肿瘤以及人类乳腺癌和结直肠癌的高转移潜能相关。将小鼠nm23-1 cDNA转染到高转移性小鼠K-1735 TK黑色素瘤细胞中,可降低原发性肿瘤形成的发生率,显著降低肿瘤转移潜能,并改变对细胞因子转化生长因子β的反应性。在此,我们讨论有关nm23的新出现的概念,例如其在肿瘤转移中不同的改变/表达模式、对肿瘤发生的影响以及可能的生化功能。

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