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SV40介导的永生化

SV40-Mediated immortalization.

作者信息

Jha K K, Banga S, Palejwala V, Ozer H L

机构信息

Department of Microbiology and Molecular Genetics, UMDNJ-New Jersey Medical School, Newark, New Jersey, 07103-2714, USA.

出版信息

Exp Cell Res. 1998 Nov 25;245(1):1-7. doi: 10.1006/excr.1998.4272.

Abstract

Human diploid cells have a limited life span, ending in replicative senescence, in contrast to cell lines derived from tumors, which show an indefinite life span and are immortal, suggesting that replicative senescence is a tumor suppression mechanism. We have utilized introduction of SV40 sequences to develop matched sets of nonimmortal and immortal cell lines to help dissect the mechanism of immortalization and have found that it has multiple facets, involving both SV40-dependent and -independent aspects. These studies have led to the identification of a novel growth suppressor gene (SEN6) as well as providing a model system for the study of cellular aging, apoptosis, and telomere stabilization among other things. It is anticipated that SV40-transformed cells will continue to provide a very useful experimental system leading to insights into the behavior of cells with altered expression of oncogenes and growth suppressor gene products.

摘要

与源自肿瘤的细胞系不同,人类二倍体细胞寿命有限,最终会进入复制性衰老,而肿瘤细胞系具有无限寿命且不死,这表明复制性衰老是一种肿瘤抑制机制。我们利用导入SV40序列来开发匹配的非永生和永生细胞系,以帮助剖析永生化机制,发现其具有多个方面,涉及SV40依赖性和非依赖性方面。这些研究不仅鉴定出一种新的生长抑制基因(SEN6),还为研究细胞衰老、凋亡和端粒稳定等提供了一个模型系统。预计SV40转化细胞将继续提供一个非常有用的实验系统,有助于深入了解癌基因和生长抑制基因产物表达改变的细胞行为。

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