| Literature DB >> 30342302 |
K P Stoltz1, C N Jondle1, K Pulakanti2, P A Sylvester1, R Urrutia3, S Rao4, V L Tarakanova5.
Abstract
Endogenous retroviruses (ERVs) comprise 10% of the genome, with many of these transcriptionally silenced post early embryogenesis. Several stimuli, including exogenous virus infection and cellular transformation can reactivate ERV expression via a poorly understood mechanism. We identified Interferon Regulatory Factor 1 (IRF-1), a tumor suppressor and an antiviral host factor, as a suppressor of ERV expression. IRF-1 decreased expression of a specific mouse ERV in vitro and in vivo. IRF-3, but not IRF-7, also decreased expression of distinct ERV families, suggesting that suppression of ERVs is a relevant biological function of the IRF family. Given the emerging appreciation of the physiological relevance of ERV expression in cancer, IRF-1-mediated suppression of specific ERVs may contribute to the overall tumor suppressor activity of this host factor.Entities:
Keywords: Cancer; Endogenous retroviruses, Interferon Regulatory Factor
Mesh:
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Year: 2018 PMID: 30342302 PMCID: PMC6875439 DOI: 10.1016/j.virol.2018.10.003
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616