Ontology highlight
ABSTRACT: Background
Caloric restriction (CR) counters deleterious effects of aging and, for most mouse genotypes, increases mean and maximum lifespan. Previous analyses of microarray data have identified gene expression responses to CR that are shared among multiple mouse tissues, including the activation of anti-oxidant, tumor suppressor and anti-inflammatory pathways. These analyses have provided useful research directions, but have been restricted to a limited number of tissues, and have focused on individual genes, rather than whole-genome transcriptional networks. Furthermore, CR is thought to oppose age-associated gene expression patterns, but detailed statistical investigations of this hypothesis have not been carried out.Results
Systemic effects of CR and aging were identifi
SUBMITTER: Swindell WR
PROVIDER: S-EPMC2795771 | biostudies-literature | 2009 Dec
REPOSITORIES: biostudies-literature