Discrete mechanisms of mTOR and cell cycle regulation by AMPK agonists independent of AMPK

Xiaona Liu(Cincinnati Children's Hospital Medical Center), Rishi Raj Chhipa, Shabnam Pooya, Matthew D. Wortman, Sara Yachyshin, Lionel M.L. Chow, Ashish Kumar(Laboratoire d’immunologie intégrative du cancer), Xuan Zhou(Laboratoire d’immunologie intégrative du cancer), Ying Sun(Cincinnati Children's Hospital Medical Center), Brian Quinn(Cincinnati Children's Hospital Medical Center), Christopher McPherson(Mayfield Brain & Spine), Ronald E. Warnick(Mayfield Brain & Spine), Ady Kendler(University of Cincinnati), Shailendra Giri(Mayo Clinic), Jeroen Poels(KU Leuven), Koen Norga(Antwerp University Hospital), Benoı̂t Viollet(Délégation Paris 5), Gregory A. Grabowski(Cincinnati Children's Hospital Medical Center), Biplab Dasgupta
Proceedings of the National Academy of Sciences
January 13, 2014
Cited by 221Open Access
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Abstract

The multifunctional AMPK-activated protein kinase (AMPK) is an evolutionarily conserved energy sensor that plays an important role in cell proliferation, growth, and survival. It remains unclear whether AMPK functions as a tumor suppressor or a contextual oncogene. This is because although on one hand active AMPK inhibits mammalian target of rapamycin (mTOR) and lipogenesis--two crucial arms of cancer growth--AMPK also ensures viability by metabolic reprogramming in cancer cells. AMPK activation by two indirect AMPK agonists AICAR and metformin (now in over 50 clinical trials on cancer) has been correlated with reduced cancer cell proliferation and viability. Surprisingly, we found that compared with normal tissue, AMPK is constitutively activated in both human and mouse gliomas. Therefore, we questioned whether the antiproliferative actions of AICAR and metformin are AMPK independent. Both AMPK agonists inhibited proliferation, but through unique AMPK-independent mechanisms and both reduced tumor growth in vivo independent of AMPK. Importantly, A769662, a direct AMPK activator, had no effect on proliferation, uncoupling high AMPK activity from inhibition of proliferation. Metformin directly inhibited mTOR by enhancing PRAS40's association with RAPTOR, whereas AICAR blocked the cell cycle through proteasomal degradation of the G2M phosphatase cdc25c. Together, our results suggest that although AICAR and metformin are potent AMPK-independent antiproliferative agents, physiological AMPK activation in glioma may be a response mechanism to metabolic stress and anticancer agents.


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