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多个基因座影响小鼠肝癌发生的遗传易感性。

Multiple loci affect genetic predisposition to hepatocarcinogenesis in mice.

作者信息

Manenti G, Binelli G, Gariboldi M, Canzian F, De Gregorio L, Falvella F S, Dragani T A, Pierotti M A

机构信息

Division of Experimental Oncology A, Istituto Nazionale Tumor, Italy.

出版信息

Genomics. 1994 Sep 1;23(1):118-24. doi: 10.1006/geno.1994.1466.

Abstract

The C3H/He mouse represents a good experimental model of genetic predisposition to hepatocellular tumor development. We analyzed an interspecific test-cross population of 106 urethane-treated male (C3H/He x Mus spretus) x C57BL/6J mice, typed with 222 genetic markers to locate precisely the hepatocellular tumor susceptibility (Hcs) loci. Three regions, on chromosomes 2, 5, and 19, showed a significant linkage with hepatocellular tumor development, as indicated by different quantitative indexes estimating liver tumor size. Liver tumor frequency was not genetically controlled. These loci are different from three other Hcs loci that we have previously mapped in an F2 progeny of the C3H/He mouse crossed with the resistant laboratory strain A/J. The present result indicates a multigenic model of inheritance for hepatocellular tumor susceptibility.

摘要

C3H/He小鼠是肝细胞肿瘤发生遗传易感性的良好实验模型。我们分析了106只经乌拉坦处理的雄性(C3H/He×小家鼠)×C57BL/6J小鼠的种间测交群体,用222个遗传标记进行分型,以精确定位肝细胞肿瘤易感性(Hcs)位点。根据估计肝肿瘤大小的不同定量指标,位于2号、5号和19号染色体上的三个区域显示出与肝细胞肿瘤发生有显著连锁。肝肿瘤发生率不受遗传控制。这些位点与我们之前在C3H/He小鼠与抗性实验室品系A/J杂交的F2后代中定位的其他三个Hcs位点不同。目前的结果表明肝细胞肿瘤易感性的多基因遗传模式。

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