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nm23转移抑制因子对信号转导的抑制作用:可能的机制

Inhibition of signal transduction by the nm23 metastasis suppressor: possible mechanisms.

作者信息

Salerno Massimiliano, Ouatas Taoufik, Palmieri Diane, Steeg Patricia S

机构信息

Women's Cancers Section, Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland 20892, USA.

出版信息

Clin Exp Metastasis. 2003;20(1):3-10. doi: 10.1023/a:1022578000022.

Abstract

The first metastasis suppressor gene identified was nm23. Transfection of nm23 into metastatic cell lines resulted in the inhibition of metastasis, but not primary tumor size in vivo. Using in vitro assays, nm23 overexpression resulted in reduced anchorage-independent colonization in response to TGF-beta, reduced invasion and motility in response to multiple factors, and increased differentiation. We hypothesize that the mechanism of action of Nm23 in metastasis suppression involves diminished signal transduction downstream of a particular receptor. Candidate biochemical mechanisms are identified and discussed herein.

摘要

第一个被鉴定出的转移抑制基因是nm23。将nm23转染至转移细胞系中可抑制体内转移,但不影响原发肿瘤大小。通过体外试验,nm23过表达可导致对转化生长因子-β(TGF-β)的非锚定依赖性集落形成减少、对多种因子的侵袭和运动能力降低以及分化增加。我们推测Nm23在转移抑制中的作用机制涉及特定受体下游信号转导的减弱。本文鉴定并讨论了可能的生化机制。

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