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Renal carcinogenesis in the Eker rat.

机译:Eker大鼠的肾脏致癌作用。

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摘要

The Eker rat hereditary renal carcinoma is an excellent example of a Mendelian dominant predisposition to a specific cancer in an experimental animal. We recently reported that a germline insertion in the rat homologue of the human tuberous sclerosis (TSC2) gene gives rise to the dominantly inherited cancer in the Eker rat model. The function of the TSC2/Tsc2 gene product (called "tuberine" in the human case) is not yet understood, although it contains a short amino acid sequence homologous to the ras family GTPase-activating proteins (GAP3). In the study, we isolated subtracted cDNA clones having increased expression in Eker renal carcinoma cells, using a modified representational difference analysis method to search for additional genes specifically involved in renal carcinogenesis. Here we identified four genes: the third component of the complement (C3) gene, the fos-related antigen I (fra-1) gene, an unknown gene (designated as being expressed in renal carcinoma: erc) and the calpactine I heavy-chain (Annexin II) gene.
机译:Eker大鼠遗传性肾癌是孟德尔对实验动物中特定癌症的易感性的一个很好的例子。我们最近报道说,在人结节性硬化症(TSC2)基因的大鼠同源物中插入种系会在Eker大鼠模型中引起显性遗传的癌症。 TSC2 / Tsc2基因产物的功能(在人的情况下称为“结核菌素”)尚不明确,尽管它含有与ras家族GTPase激活蛋白(GAP3)同源的短氨基酸序列。在这项研究中,我们使用改良的代表性差异分析方法搜索了专门参与肾脏癌变的其他基因,从而在Eker肾癌细胞中分离了表达减少的cDNA克隆。在这里,我们确定了四个基因:补体(C3)基因的第三部分,与fos相关的抗原I(fra-1)基因,一个未知基因(指定为在肾癌中表达的erc)和重度钙铁蛋白I链(Annexin II)基因。

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