Critical role for SV40 small-t antigen in human cell transformation

被引:114
作者
Yu, J
Boyapati, A
Rundell, K
机构
[1] Northwestern Univ, Dept Microbiol Immunol, Chicago, IL 60611 USA
[2] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
关键词
SV40; small-t antigen; transformation; human fibroblasts; human mesothelial cells;
D O I
10.1006/viro.2001.1204
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Defining the ability of simian virus 40 (SV40) to transform human cells has become of even greater importance with the increased understanding that this virus may play a role in some human malignancies. This report documents the requirement for viral small-t (ST) antigen in large-T (LT)-driven transformation of primary fibroblasts, a requirement that cannot be met by a well-known oncogene, c-Ha-ras (EJ-ras), which can cooperate with LT in rodent systems. The cellular gene telomerase is not essential for transformation, although transformed clones are not immortal without it. Similarly, an immortal mesothelial cell line has been developed using LT and telomerase. Immortalized mesothelial cells are morphologically normal, but can be transformed by introduction of ST, or ST + ras, but not by ras alone. It is likely that ST will be required along with LT for transformation of most human cell types. (C) 2001 Academic Press.
引用
收藏
页码:192 / 198
页数:7
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