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通过在埃克大鼠肾癌细胞中替换Tsc2基因来抑制肿瘤表型。

Suppression of the neoplastic phenotype by replacement of the Tsc2 gene in Eker rat renal carcinoma cells.

作者信息

Orimoto K, Tsuchiya H, Kobayashi T, Matsuda T, Hino O

机构信息

Department of Experimental Pathology, Cancer Institute, Tokyo, Japan.

出版信息

Biochem Biophys Res Commun. 1996 Feb 6;219(1):70-5. doi: 10.1006/bbrc.1996.0183.

Abstract

The hereditary renal carcinoma (RC) in the rat, originally reported by R. Eker in 1954, is an excellent example of a Mendelian dominantly inherited predisposition to a specific cancer in an experimental animal. Recently, we have identified a germline mutation of the sclerosis (Tsc2) gene in the Eker rat (Nature Genetics 9, 70-74, 1995), suggested to be a novel tumor suppressor gene, fitting Knudson's two-hit hypothesis. In this study, the effect of wild-type Tsc2 gene expression in Eker RC cells was tested using a tetracycline-responsive promoter system. Transfection and expression of a exogenous Tsc2 gene affected both cell morphology and growth rate. This demonstration of suppression of the neoplastic phenotype provides direct evidence for an essential role of the Tsc2 gene in tumorigenesis.

摘要

1954年由R. 埃克首次报道的大鼠遗传性肾癌(RC),是实验动物中孟德尔显性遗传易患特定癌症的一个典型例子。最近,我们在埃克大鼠中鉴定出硬化(Tsc2)基因的种系突变(《自然遗传学》第9卷,第70 - 74页,1995年),该基因被认为是一种新型肿瘤抑制基因,符合克努森的双击假说。在本研究中,使用四环素反应性启动子系统测试了野生型Tsc2基因在埃克肾癌细胞中的表达效果。外源性Tsc2基因的转染和表达影响了细胞形态和生长速率。这种对肿瘤表型抑制的证明为Tsc2基因在肿瘤发生中的重要作用提供了直接证据。

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