T antigen transgenic mouse models.

Abstract:

:The study of polyomavirus has benefited immensely from two scientific methodologies, cell culture and in vitro studies on one side and the use of transgenic mice as experimental models on the other. Both approaches allowed us to identify cellular products targeted by the viruses, the consequences of these interactions at the phenotypic and molecular level, and thus the potential roles of the targets within their normal cellular context. In particular, cell culture and in vitro reports suggest a model explaining partially how SV40 large T antigen contributes to oncogenic transformation. In most cases, T antigen induces cell cycle entry by inactivation of the Rb proteins (pRb, p130, and p107), thus activating E2F-dependent transcription and subsequent S-phase entry. Simultaneously, T antigen blocks p53 activity and therefore prevents the ensuing cell-cycle arrest and apoptosis. For the most part, studies of T antigen expression in transgenic mice support this model, but the use of T antigen mutants and their expression in different tissue and cell type settings have expanded our knowledge of the model system and raised important questions regarding tumorigenic mechanisms functioning in vivo.

journal_name

Semin Cancer Biol

authors

Sáenz Robles MT,Pipas JM

doi

10.1016/j.semcancer.2009.02.002

subject

Has Abstract

pub_date

2009-08-01 00:00:00

pages

229-35

issue

4

eissn

1044-579X

issn

1096-3650

pii

S1044-579X(09)00003-0

journal_volume

19

pub_type

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