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DOI: 10.1126/science.1215327
¤ OpenAccess: Bronze
This work has “Bronze” OA status. This means it is free to read on the publisher landing page, but without any identifiable license.

The Ancient Drug Salicylate Directly Activates AMP-Activated Protein Kinase

Simon A. Hawley,Morgan D. Fullerton,Fiona A. Ross,Jonathan D. Schertzer,Cyrille Chevtzoff,Katherine J. Walker,Mark Peggie,Darya Zibrova,Kevin A. Green,Kirsty J. Mustard,Bruce E. Kemp,Kei Sakamoto,Gregory R. Steinberg,D. Grahame Hardie

AMPK
AMP-activated protein kinase
Protein kinase A
2012
An Aspirin a Day? The protein kinase AMPK (adenosine monophosphate–activated protein kinase) directly monitors cellular energy stores as reflected by changes in cellular concentrations of AMP, adenosine diphosphate (ADP), and adenosine triphosphate (ATP). Through phosphorylation of its targets, it helps to control metabolism, polarity, autophagy, and the restraint of cell proliferation. Activation of AMPK is also proposed to be beneficial for the treatment of diseases, including cancer and diabetes. Hawley et al. (p. 918 , published online 19 April; see the Perspective by Shaw and Cantley ) report that AMPK can be activated by high concentrations of salicylate, a compound derived from the very commonly used drug aspirin. In mice, salicylate promoted fatty acid and carbohydrate metabolism in an AMPK-dependent fashion.
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    The Ancient Drug Salicylate Directly Activates AMP-Activated Protein Kinase” is a paper by Simon A. Hawley Morgan D. Fullerton Fiona A. Ross Jonathan D. Schertzer Cyrille Chevtzoff Katherine J. Walker Mark Peggie Darya Zibrova Kevin A. Green Kirsty J. Mustard Bruce E. Kemp Kei Sakamoto Gregory R. Steinberg D. Grahame Hardie published in 2012. It has an Open Access status of “bronze”. You can read and download a PDF Full Text of this paper here.