Title | Dissecting the Dual Role of AMPK in Cancer: From Experimental to Human Studies. |
Publication Type | Journal Article |
Year of Publication | 2015 |
Authors | Zadra G, Batista JL, Loda M |
Journal | Mol Cancer Res |
Volume | 13 |
Issue | 7 |
Pagination | 1059-72 |
Date Published | 2015 Jul |
ISSN | 1557-3125 |
Keywords | AMP-Activated Protein Kinases, Animals, Antineoplastic Agents, Cell Hypoxia, Cell Proliferation, Genes, Tumor Suppressor, Humans, Neoplasms, Oncogenes, Stress, Physiological |
Abstract | The precise role of 5'AMP-activated kinase (AMPK) in cancer and its potential as a therapeutic target is controversial. Although it is well established that activation of this energy sensor inhibits the main anabolic processes that sustain cancer cell proliferation and growth, AMPK activation can confer on cancer cells the plasticity to survive under metabolic stress such as hypoxia and glucose deprivation, which are commonly observed in fast growing tumors. Thus, AMPK is referred to as both a "conditional" tumor suppressor and "contextual" oncogene. To add a further layer of complexity, AMPK activation in human cancer tissues and its correlation with tumor aggressiveness and progression appears to vary in different contexts. The current review discusses the different faces of this metabolic regulator, the therapeutic implications of its modulation, and provides an overview of the most relevant data available on AMPK activation and AMPK-activating drugs in human studies. |
DOI | 10.1158/1541-7786.MCR-15-0068 |
Alternate Journal | Mol Cancer Res |
PubMed ID | 25956158 |
PubMed Central ID | PMC4504770 |
Grant List | P50 CA090381 / CA / NCI NIH HHS / United States R01 CA187918 / CA / NCI NIH HHS / United States R01 CA131945 / CA / NCI NIH HHS / United States 2R01CA131945 / CA / NCI NIH HHS / United States P50 CA90381 / CA / NCI NIH HHS / United States |
Related Faculty:
Massimo Loda, M.D.