| Literature DB >> 28065746 |
Andrea Morandi1, Stefano Indraccolo2.
Abstract
Metabolic rearrangements are essential to satisfy the different requirements of cancer cells during tumorigenesis and recent studies have highlighted a role for such metabolic reprogramming in response and adaptation to therapies. However, therapy-resistant experimental models have been described to be either glycolysis-dependent or OXPHOS-addicted. Here we discuss the recent literature on metabolic reprogramming of cancer in therapy resistance with a plausible explanation of the observed differences which collectively indicate that dis-regulated metabolic pathways could be considered potential therapeutic targets in tumors resistant to conventional therapy.Entities:
Keywords: Metabolic reprogramming; OXPHOS; Therapy resistance; Warburg metabolism
Mesh:
Year: 2017 PMID: 28065746 DOI: 10.1016/j.bbcan.2016.12.004
Source DB: PubMed Journal: Biochim Biophys Acta Rev Cancer ISSN: 0304-419X Impact factor: 10.680