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携带人类原型c-HRAS基因的转基因小鼠快速致癌性检测系统

Rapid carcinogenicity testing system with transgenic mice harboring human prototype c-HRAS gene.

作者信息

Yamamoto S, Hayashi Y, Mitsumori K, Nomura T

机构信息

Department of Pharmacology, School of Medicine, Keio University, Tokyo, Japan.

出版信息

Lab Anim Sci. 1997 Apr;47(2):121-6.

PMID:9150488
Abstract

Rapid carcinogenicity tests were done with transgenic (Tg) mice human prototype c-HRAS gene, namely BALB/cByJ x C57BL/6JF1-TgN(HRAS)2 or CB6F1-HRAS2 mice. The studies were conducted as the first step in the evaluation of the CB6F1-HRAS2 mouse as a model for the rapid carcinogenicity testing system. Results of short-term tests of various genotoxic carcinogens indicated that CB6F1-HRAS2 mice are more susceptible to these carcinogens than control non-Tg mice. According to the first-step evaluation studies, more rapid onset and a higher incidence of more malignant tumors can be expected with a higher probability after treatment with various genotoxic carcinogens in the CB6F1-HRAS2 mice than in control non-Tg mice. The CB6F1-HRAS2 mouse seems to be a promising candidate as an animal model for the development of a rapid carcinogenicity testing system.

摘要

利用转基因(Tg)小鼠人源原型c-HRAS基因,即BALB/cByJ×C57BL/6JF1-TgN(HRAS)2或CB6F1-HRAS2小鼠进行了快速致癌性试验。这些研究作为将CB6F1-HRAS2小鼠评估为快速致癌性测试系统模型的第一步开展。各种遗传毒性致癌物短期试验的结果表明,CB6F1-HRAS2小鼠比对照非转基因小鼠对这些致癌物更敏感。根据第一步评估研究,与对照非转基因小鼠相比,用各种遗传毒性致癌物处理后,CB6F1-HRAS2小鼠更有可能更快发病且发生更多恶性肿瘤的概率更高。CB6F1-HRAS2小鼠似乎是开发快速致癌性测试系统的动物模型的一个有前景的候选者。

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