Involvement of AMP-Activated protein kinase and p38 mitogen-activated protein kinase in 8-Cl-cAMP-Induced growth inhibition

J. E.E.Hae Han, A. H.N. Young-Ho, K. I.Young Choi, Seung Hwan Hong

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


8-Cl-cAMP (8-chloro-cyclic AMP), which induces differentiation, growth inhibition and apoptosis in various cancer cells, has been investigated as a putative anti-cancer drug. Although we reported that 8-Cl-cAMP induces growth inhibition via p38 mitogen-activated protein kinase (MAPK) and a metabolite of 8-Cl-cAMP, 8-Cl-adenosine mediates this process, the action mechanism of 8-Cl-cAMP is still uncertain. In this study, it was found that 8-Cl-cAMP-induced growth inhibition is mediated by AMP-activated protein kinase (AMPK) 8-Cl-cAMP was shown to activate AMPK, which was also dependent on the metabolic degradation of 8-Cl-cAMP. A potent agonist of AMPK, 5-aminoimidazole-4- carboxamide ribonucleoside (AICAR) could also induce growth inhibition and apoptosis. To further delineate the role of AMPK in 8-Cl-cAMP-induced growth inhibition and apoptosis, we used two approaches: pharmacological inhibition of the enzyme with compound C and expression of a dominant negative mutant (a kinase-dead form of AMPKα2, KD-AMPK). AICAR was able to activate p38 MAPK and pre-treatment with AMPK inhibitor or expression of KD-AMPK blocked this p38 MAPK activation. Cell growth inhibition was also attenuated. Furthermore, p38 MAPK inhibitor attenuated 8-Cl-cAMP- or AICAR-induced growth inhibition but had no effect on AMPK activation. These results demonstrate that 8-Cl-cAMP induced growth inhibition through AMPK activation and p38 MAPK acts downstream of AMPK in this signaling pathway.

Original languageEnglish
Pages (from-to)104-112
Number of pages9
JournalJournal of Cellular Physiology
Issue number1
StatePublished - Jan 2009


Dive into the research topics of 'Involvement of AMP-Activated protein kinase and p38 mitogen-activated protein kinase in 8-Cl-cAMP-Induced growth inhibition'. Together they form a unique fingerprint.

Cite this