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| Content Provider | PubMed Central |
|---|---|
| Author | Park, Sunghee Chang, Ching-yi Safi, Rachid Liu, Xiaojing Baldi, Robert Jasper, Jeff S. Anderson, Grace R. Liu, Tingyu Rathmell, Jeffrey C. Dewhirst, Mark W. Wood, Kris C. Locasale, Jason W. Mcdonnell, Donald P. |
| Abstract | Imaging studies in animals and in humans have indicated that the oxygenation and nutritional status of solid tumors is dynamic. Further, the extremely low level of glucose within tumors, while reflecting its rapid uptake and metabolism, also suggests that cancer cells must rely on other energy sources in some circumstances. Here we find that some breast cancer cells can switch to utilizing lactate as a primary source of energy, allowing them to survive glucose deprivation for extended periods, and that this activity confers resistance to PI3K/mTOR inhibitors. The nuclear receptor, estrogen-related receptor alpha (ERRα), was shown to regulate the expression of genes required for lactate utilization and isotopomer analysis revealed that genetic or pharmacological inhibition of ERRα activity compromised lactate oxidation. Importantly, ERRα antagonists increased the in vitro and in vivo efficacy of PI3K/mTOR inhibitors, highlighting the potential clinical utility of this drug combination. |
| Related Links | http://dx.doi.org/10.1016/j.celrep.2016.03.026 |
| Ending Page | 335 |
| Page Count | 13 |
| Starting Page | 323 |
| File Format | |
| ISSN | 22111247 |
| e-ISSN | 22111247 |
| Journal | Cell reports |
| Issue Number | 2 |
| Volume Number | 15 |
| Language | English |
| Publisher Date | 2016-04-12 |
| Access Restriction | Open |
| Subject Keyword | Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Biochemistry, Genetics and Molecular Biology |
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