Cicala C, Pompetti F, Carbone M
Section on Viruses and Cellular Biology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892.
Am J Pathol. 1993 May;142(5):1524-33.
In the course of studies to elucidate the relative contribution of simian virus 40 (SV40) large T and small t proteins during oncogenesis, we observed the appearance of pericardial and pleural tumors in 100% of Syrian hamsters injected in the pleural space with wild type SV40. When SV40 was injected via the intracardiac or intraperitoneal routes, more than 50% of hamsters developed mesothelial tumors. Macroscopic, microscopic, ultramicroscopic, and histochemical characteristics identify these neoplasms and derived cell lines as mesotheliomas and mesothelioma-derived cell lines. The SV40 genome was integrated and expressed in the mesotheliomas and derived cell lines. The absence of mesotheliomas in hamsters injected with SV40 small t deletion mutants indicates that the small t protein plays an important role in the development of SV40-induced mesotheliomas. To the best of our knowledge, this is the first definitive report of virus-induced mesotheliomas in mammals.
在阐明猴病毒40(SV40)大T蛋白和小t蛋白在肿瘤发生过程中的相对贡献的研究过程中,我们观察到,100%经胸膜腔注射野生型SV40的叙利亚仓鼠出现了心包和胸膜肿瘤。当通过心内或腹腔途径注射SV40时,超过50%的仓鼠发生了间皮瘤。宏观、微观、超微和组织化学特征将这些肿瘤及衍生的细胞系鉴定为间皮瘤和间皮瘤衍生的细胞系。SV40基因组在间皮瘤和衍生的细胞系中整合并表达。注射SV40小t缺失突变体的仓鼠未出现间皮瘤,这表明小t蛋白在SV40诱导的间皮瘤发生中起重要作用。据我们所知,这是关于哺乳动物中病毒诱导间皮瘤的第一份确切报告。