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 Suppression of protein kinase C and nuclear oncogene expression as possible  action mechanisms of cancer chemoprevention by Curcumin Lin JKArch Pharm Res  2004[Jul]; 27 (7): 683-92Curcumin (diferuloylmethane) is a major naturally-occurring polyphenol of Curcuma  species, which is commonly used as a yellow coloring and flavoring agent in  foods. Curcumin has shown anti-carcinogenic activity in animal models. Curcumin  possesses anti-inflammatory activity and is a potent inhibitor of reactive  oxygen-generating enzymes such as lipoxygenase/cyclooxygenase, xanthine  dehydrogenase/oxidase and inducible nitric oxide synthase; and an effective  inducer of heme oxygenase-1. Curcumin is also a potent inhibitor of protein  kinase C (PKC), EGF(Epidermal growth factor)-receptor tyrosine kinase and IkappaB  kinase. Subsequently, curcumin inhibits the activation of NF(nucleor  factor)kappaB and the expressions of oncogenes including c-jun, c-fos, c-myc,  NIK, MAPKs, ERK, ELK, PI3K, Akt, CDKs and iNOS. It is proposed that curcumin may  suppress tumor promotion through blocking signal transduction pathways in the  target cells. The oxidant tumor promoter TPA activates PKC by reacting with zinc  thiolates present within the regulatory domain, while the oxidized form of cancer  chemopreventive agent such as curcumin can inactivate PKC by oxidizing the  vicinal thiols present within the catalytic domain. Recent studies indicated that  proteasome-mediated degradation of cell proteins play a pivotal role in the  regulation of several basic cellular processes including differentiation,  proliferation, cell cycling, and apoptosis. It has been demonstrated that  curcumin-induced apoptosis is mediated through the impairment of  ubiquitin-proteasome pathway. Curcumin was first biotransformed to  dihydrocurcumin and tetrahydrocurcumin and that these compounds subsequently were  converted to monoglucuronide conjugates. These results suggest that  curcumin-glucuronide, dihydrocurcumin-glucuronide, tetrahydrocurcumin-glucuronide  and tetrahydrocurcumin are the major metabolites of curcumin in mice, rats and  humans.|Animals[MESH]|Anticarcinogenic Agents/pharmacokinetics/*pharmacology[MESH]|Biotransformation[MESH]|Cell Nucleus/genetics[MESH]|Curcumin/pharmacokinetics/*pharmacology[MESH]|Gene Expression Regulation, Neoplastic/*drug effects[MESH]|Humans[MESH]|Neoplasms/*genetics/*prevention & control[MESH]|Oncogenes/*genetics[MESH]|Protein Kinase C/*antagonists & inhibitors[MESH]
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