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A Novel Gene Niban Upregulated in Renal Carcinogenesis: Cloning by the cDNA‐amplified Fragment Length Polymorphism Approach

机译:肾癌中上调的新型基因 Niban:通过cDNA扩增的片段长度多态性方法克隆

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摘要

A modified AFLP (amplified fragment length polymorphism) method was employed to isolate genes differentially expressed in renal carcinogenesis of Tsc2 gene mutant (Eker) rats. One gene, selected for further investigation, was named “Niban” (“second” in Japanese), because it is the second new gene to be found after Erc (expressed in renal carcinoma) in our laboratory. Importantly, “Niban” is well expressed even in small primary rat Eker renal tumors, more than in progressed cell lines, and is also expressed in human renal carcinoma cells, but not in normal human or rat kidneys. Chromosome assignment was to RNO 13 in the rat, and HSA 1. This “Niban” gene is a candidate as a marker for renal tumor, especially early‐stage renal carcinogenesis.
机译:改良的AFLP(扩增片段长度多态性)方法用于分离在Tsc2基因突变(Eker)大鼠的肾癌中差异表达的基因。一个被选择进行进一步研究的基因被命名为“ Niban”(日语中为“第二”),因为它是在我们实验室中发现的第二个新基因,仅次于Erc(在肾癌中表达)。重要的是,即使在小的原发性大鼠Eker肾肿瘤中,“ Niban”也能很好地表达,而不是在进展中的细胞系中表达,而且在人肾癌细胞中也能表达,但在正常人或大鼠肾脏中却不表达。大鼠和HSA 1中的染色体分配与RNO 13有关。该“ Niban”基因可作为肾肿瘤,尤其是早期肾癌发生的标志物。

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