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Carcinogenesis Advance Access published online on May 13, 2008

Carcinogenesis, doi:10.1093/carcin/bgn114
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© The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Curcumin decreases 12-0-tetradecanoylphorbol-13-acetate-induced protein kinase C translocation to modulate downstream targets in mouse skin

Rachana Garg, Asha Ramchandani and Girish Maru*

Advanced Centre for Treatment, Research and Education in Cancer (ACTREC), Tata Memorial Centre, Kharghar, Navi Mumbai-410 208, India

* Corresponding Author: Tel: 91-22-27405022. Fax: 91-22-27405085; 91-22-27415894. E-mail: gmaru{at}actrec.gov.in

Curcumin has been shown to inhibit 12-O-tetradecanoyl-phorbol-13-acetate (TPA)-induced tumor promotion and some of the TPA-responsive markers in mouse skin. However, its mechanism of action is not fully elucidated. The present study focuses on understanding the role of protein kinase C (PKC), the major cellular receptor of TPA, in mediating TPA-induced biological responses in mouse skin and subsequently, elucidating the effect(s) of curcumin on PKC and its downstream target molecules. As compared to controls, single topical application of TPA (5 nmol) to skin increased the translocation of PKC from cytosolic to particulate fraction; determined in terms of activity and protein levels. Ro-31-8220 (PKC inhibitor, 1nmol) when applied topically, alone or prior to TPA, inhibited PKC activity in both the compartments but did not affect the TPA-induced protein translocation. In contrast, though curcumin (10 µmol) alone did not alter the basal activity/levels, its pre-treatment decreased the TPA-induced translocation of PKC isozymes ({alpha}, β, {gamma}, {epsilon}, {eta}), resulting in appropriate alterations in activity. Despite differences in modes of action of Ro-31-8220 (activity inhibition) and curcumin (decreasing translocation) in modulating PKC, their pre-treatment blunted the TPA-induced levels of mitogen-activated protein kinases and transcription factors (c-jun, c-fos, NF-{kappa}B) and downstream target proteins associated with cell proliferation (cyclin D1, ODC), cell death (Bax, Bcl2), inflammation (COX-2, PGE2) and oxidative stress (8-OH-dG) in skin. These results demonstrate the crucial role of PKC in TPA-mediated cellular responses in skin and that curcumin modulates trans-membrane signal transduction via PKC to affect TPA-induced biochemical and molecular alterations in mouse skin.

Received March 14, 2008; revised April 25, 2008; accepted April 29, 2008.


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