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PMID: 12807725 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Curcumin (diferuloylmethane) down-regulates cigarette smoke-induced NF-kappaB activation through inhibition of IkappaBalpha kinase in human lung epithelial cells: correlation with suppression of COX-2, MMP-9 and cyclin D1.

Carcinogenesis ·Vol. 24 ·No. 7 ·2003-07-00 ·Pages 1269-79

Shishodia S, Potdar P, Gairola CG, Aggarwal BB

Abstract

Cigarette smoke (CS) is a major cause of a variety of malignancies including cancers of the larynx, oral cavity and pharynx, esophagus, pancreas, kidney, bladder and lung. The signal transduction pathway that mediates the effects of CS is not well understood but nuclear factor-kappa B (NF-kappaB) is probably involved. The gas phase of CS contains free radicals such as superoxide radicals, hydroxyl radicals and hydrogen peroxide, which potentially can activate NF-kappaB. Benzo[a]pyrene, another potent carcinogen of CS, can also activate NF-kappaB, but by an as yet unknown mechanism. Various other agents that activate NF-kappaB are either tumor initiators or tumor promoters, and NF-kappaB activation can block apoptosis, promote proliferation and mediate tumorigenesis. Therefore, NF-kappaB is an ideal target for preventing CS-induced lung carcinogenesis. Thus, agents that abrogate NF-kappaB activation have the potential to suppress lung carcinogenesis. Because curcumin, a diferuloylmethane, is anticarcinogenic, we investigated the effect of this phytochemical on CS-induced NF-kappaB activation and NF-kappaB-regulated gene expression in human non-small cell lung carcinoma cells. Exposure of cells to CS induced persistent activation of NF-kappaB, and pre-treatment with curcumin abolished the CS-induced DNA-binding of NF-kappaB, IkappaBalpha kinase activation, IkBalpha phosphorylation and degradation, p65 nuclear translocation and CS-induced NF-kappaB-dependent reporter gene expression. The inhibition of NF-kappaB activation correlated with suppression of CS-induced NF-kappaB-dependent cyclin D1, cyclooxygenase-2 and matrix metalloproteinase-9 expression. Overall our results indicate that CS-induced NF-kappaB activation and NF-kappaB-regulated gene expression in human non-small cell lung carcinoma cells is suppressed by curcumin through suppression of IkappaBalpha kinase.

MeSH Terms
Antineoplastic Agents/pharmacology Blotting, Western Carcinoma, Non-Small-Cell Lung/metabolism,pathology Cells, Cultured Curcumin/pharmacology Cyclin D1/metabolism Cyclooxygenase 2 DNA Primers/chemistry Down-Regulation/drug effects Epithelial Cells/drug effects Humans I-kappa B Kinase Isoenzymes/metabolism Luciferases/metabolism Lung Neoplasms/metabolism,pathology Matrix Metalloproteinase 9/metabolism Membrane Proteins NF-kappa B/metabolism Phosphorylation Prostaglandin-Endoperoxide Synthases/metabolism Protein Serine-Threonine Kinases/antagonists & inhibitors RNA, Messenger/metabolism Reverse Transcriptase Polymerase Chain Reaction Smoking/adverse effects Transfection
Chemicals
Antineoplastic Agents DNA Primers Isoenzymes Membrane Proteins NF-kappa B RNA, Messenger Cyclin D1 Luciferases Cyclooxygenase 2 PTGS2 protein, human Prostaglandin-Endoperoxide Synthases Protein Serine-Threonine Kinases CHUK protein, human I-kappa B Kinase IKBKB protein, human IKBKE protein, human Matrix Metalloproteinase 9 Curcumin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shishodia Shishir
Cytokine Research Laboratory, Department of Bioimmunotherapy, The University of Texas M. D. Anderson Cancer Center, Box 143, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Potdar Pravin
Gairola C Gary
Aggarwal Bharat B
Article Info
Journal
Carcinogenesis
Abbr.
Carcinogenesis
ISSN
0143-3334
Published
2003-07-00
Epub
2003-00-09
Pages
1269-79
Language
English
Region
England
NLM ID
8008055
Subset
IM
Grants
NCI NIH HHS · CA91844 · United States
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