TY - JOUR
T1 - Caloric restriction mimetics
T2 - Towards a molecular definition
AU - Madeo, Frank
AU - Pietrocola, Federico
AU - Eisenberg, Tobias
AU - Kroemer, Guido
N1 - Funding Information:
The authors are supported by the Ligue contre le Cancer (équipe labellisée), Agence National de la Recherche, Association pour la Recherche sur le Cancer, Cancéropôle Ile-de-France, Institut National du Cancer (INCa), Fondation Bettencourt-Schueller, Fondation de France, Fondation pour la Recherche Médicale, the European Commission (ArtForce), the European Research Council, the LabEx Immuno-Oncology, the SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (Socrate), Cancer Research and Personalized Medicine (Carpem) and the Paris Alliance of Cancer Research Institutes. T.E. is a recipient of an APART (Austrian Programme for Advanced Research and Technology) fellowship of the Austrian Academy of Sciences at the Institute of Molecular Biosciences, University of Graz, Austria. F.M. is supported by the Austrian Science Fund FWF (grants LIPOTOX, I1000, P23490-B12 and P24381-B20).
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Caloric restriction, be it constant or intermittent, is reputed to have health-promoting and lifespan-extending effects. Caloric restriction mimetics (CRMs) are compounds that mimic the biochemical and functional effects of caloric restriction. In this Opinion article, we propose a unifying definition of CRMs as compounds that stimulate autophagy by favouring the deacetylation of cellular proteins. This deacetylation process can be achieved by three classes of compounds that deplete acetyl coenzyme A (AcCoA; the sole donor of acetyl groups), that inhibit acetyl transferases (a group of enzymes that acetylate lysine residues in an array of proteins) or that stimulate the activity of deacetylases and hence reverse the action of acetyl transferases. A unifying definition of CRMs will be important for the continued development of this class of therapeutic agents.
AB - Caloric restriction, be it constant or intermittent, is reputed to have health-promoting and lifespan-extending effects. Caloric restriction mimetics (CRMs) are compounds that mimic the biochemical and functional effects of caloric restriction. In this Opinion article, we propose a unifying definition of CRMs as compounds that stimulate autophagy by favouring the deacetylation of cellular proteins. This deacetylation process can be achieved by three classes of compounds that deplete acetyl coenzyme A (AcCoA; the sole donor of acetyl groups), that inhibit acetyl transferases (a group of enzymes that acetylate lysine residues in an array of proteins) or that stimulate the activity of deacetylases and hence reverse the action of acetyl transferases. A unifying definition of CRMs will be important for the continued development of this class of therapeutic agents.
UR - http://www.scopus.com/inward/record.url?scp=84921798595&partnerID=8YFLogxK
U2 - 10.1038/nrd4391
DO - 10.1038/nrd4391
M3 - Review article
C2 - 25212602
AN - SCOPUS:84921798595
SN - 1474-1776
VL - 13
SP - 727
EP - 740
JO - Nature Reviews Drug Discovery
JF - Nature Reviews Drug Discovery
IS - 10
ER -