| Literature DB >> 24530513 |
Claudia Cerella1, Anthoula Gaigneaux1, Mario Dicato1, Marc Diederich2.
Abstract
Cells reprogram their metabolism very early during carcinogenesis; this event is critical for the establishment of other cancer hallmarks. Many oncogenes and tumor suppressor genes control metabolism by interplaying with the existing nutrient-sensing intracellular pathways. Mammalian target of rapamycin, mTOR, is emerging as a collector and sorter of a metabolic network controlling upstream and downstream modulation of these same genes. Natural compounds represent a source of anti-cancer molecules with chemopreventive and therapeutic properties. This review describes selected pathways and genes orchestrating the metabolic reprogramming and discusses the potential of natural compounds to target oncogenic metabolic aberrations.Entities:
Keywords: Cancer; Metabolism; Natural compounds; mTOR
Mesh:
Substances:
Year: 2014 PMID: 24530513 DOI: 10.1016/j.canlet.2014.02.008
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679