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猿猴病毒40大T抗原表达与转基因小鼠肿瘤形成之间的关系。

Relationship between simian virus 40 large tumor antigen expression and tumor formation in transgenic mice.

作者信息

Van Dyke T A, Finlay C, Miller D, Marks J, Lozano G, Levine A J

出版信息

J Virol. 1987 Jun;61(6):2029-32. doi: 10.1128/JVI.61.6.2029-2032.1987.

Abstract

A line of transgenic mice containing the simian virus 40 (SV40) large tumor antigen gene under the control of the viral enhancer-promoter expressed this viral protein in the brains of these mice within the first 2 weeks after birth. Multiple foci of anaplastic cells formed in the choroid plexuses of these mice at 36 to 41 days after birth, and normal tissue coexisted with these transformed foci. Immunoperoxidase staining to detect the SV40 T antigen showed tumor-specific expression of nuclear T antigen at late times in tumor development, approximately 90 to 100 days and thereafter. The level of SV40 T antigen, on a per cell basis, appeared to be lower in the great majority of choroid plexus cells at earlier times in tumor development. These results suggest that low levels of tumor antigen (14 to 36 days) are present before detectable pathology (36 to 41 days) and the level of T antigen per cell is higher in rapidly growing late-stage tumors (older than 90 days).

摘要

在病毒增强子-启动子控制下含有猿猴病毒40(SV40)大肿瘤抗原基因的转基因小鼠品系,在出生后的头2周内在这些小鼠的大脑中表达了这种病毒蛋白。出生后36至41天,这些小鼠的脉络丛中形成了多个间变性细胞灶,正常组织与这些转化灶共存。免疫过氧化物酶染色检测SV40 T抗原显示,在肿瘤发展后期,大约90至100天及之后,核T抗原呈肿瘤特异性表达。在肿瘤发展的早期,绝大多数脉络丛细胞中,基于每个细胞计算的SV40 T抗原水平似乎较低。这些结果表明,在可检测到病理变化(36至41天)之前就存在低水平的肿瘤抗原(14至36天),并且在快速生长的晚期肿瘤(90天以上)中每个细胞的T抗原水平更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0596/254213/0c09f4bccc9a/jvirol00097-0274-a.jpg

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