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.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.bbcan.2016.12.004 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!