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[Nuclear FoxO1 as a bridge beetwen metabolism and mitogenesis.]

Authors :
Naïmi, Mourad
Van Obberghen, E.
Laboratoire de biochimie
Hôpital Pasteur [Nice] (CHU)-Centre Hospitalier Universitaire de Nice (CHU Nice)
Dysfonctions métaboliques et diabètes: Mécanismes et approches thérapeutiques
Université Nice Sophia Antipolis (... - 2019) (UNS)
COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-IFR50-Institut National de la Santé et de la Recherche Médicale (INSERM)
Université Nice Sophia Antipolis (1965 - 2019) (UNS)
Naïmi, Mourad
Source :
médecine/sciences, médecine/sciences, EDP Sciences, 2008, 24 (6-7), pp.635-40
Publication Year :
2008
Publisher :
HAL CCSD, 2008.

Abstract

National audience; The transcription factor FoxO1 plays a central role in the metabolic adaptations to fasting. Furthermore, FoxO1 and its homologs encode enzymes buffering ROS (reactive oxygen species) or repairing damaged DNA, and are involved in stalling the ageing process across evolution. Our recent work conducted in primary cultures of rat hepatocytes suggests new mechanisms by which Foxo1 exerts some of these functions. They revealed an unexpected role for Foxo1 in amplifying metabolic, survival, mitogenic and stress signals, and the existence of multiple feed-back loops by which Foxo1 integrates and controls these pathways. Furthermore, these effects were found to be independent of Foxo1 direct binding to DNA. double dagger.

Details

Language :
French
ISSN :
07670974 and 19585381
Database :
OpenAIRE
Journal :
médecine/sciences, médecine/sciences, EDP Sciences, 2008, 24 (6-7), pp.635-40
Accession number :
edsair.dedup.wf.001..cb08a7d8d3f3acdcb4ac4aefe55a23f1