| Literature DB >> 16044420 |
Masaaki Nomura1, Daisuke Ichimatsu, Shuzo Moritani, Ichiko Koyama, Zigang Dong, Koichi Yokogawa, Ken-Ichi Miyamoto.
Abstract
We found that caffeine significantly inhibited epidermal growth factor (EGF)- and 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced cell transformation in the JB6 mouse epidermal cell line. The tumor promoter-induced cell transformation was also blocked by treatment with an adenosine A1 receptor antagonist, 8-phenyltheophylline (8-PTH). Caffeine slightly attenuated activation of EGF-induced activator protein 1 (AP-1) activation, which play important roles in cell transformation, but only at the highest concentration examined (1 mM). Interestingly, pretreatment with caffeine suppressed EGF-induced phosphorylation and activation of Akt and ribosomal p 70 S6 protein kinase (p 70 S 6 K), a target of Akt, without inhibiting phosphatidylinositol 3-kinase (PI 3 K) activation. The inhibition of Akt activation of caffeine was not a result of its adenosine receptor antagonism. Because Akt plays a key role in signal transduction pathways leading to cell proliferation and apoptosis, our results provide novel insight into possible mechanisms of the chemotherapeutic effect of caffeine. (c) 2005 Wiley-Liss, Inc.Entities:
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Year: 2005 PMID: 16044420 DOI: 10.1002/mc.20120
Source DB: PubMed Journal: Mol Carcinog ISSN: 0899-1987 Impact factor: 4.784