Abstract
It has been shown that inhibition of cyclooxygenase 2 (COX-2) may cause growth arrest and reduced tumour formation in some human cancers; however, the mechanism is not fully known. In this study, we used an oral squamous cell carcinoma cell line to study growth inhibition and changes in critical cell cycle-regulating proteins induced by the selective COX-2 inhibitor celecoxib. Using cell viability assay, we established the optimal in vitro inhibitory dose of celecoxib and showed that inhibition of COX-2 markedly induces the expression of p27kip1, p21, waf1, and the F-box protein skp2. These results add new experimental data to our knowledge of the mechanism of cyclooxygenases on neoplastic cells.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Carcinoma, Squamous Cell / drug therapy*
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Carcinoma, Squamous Cell / metabolism
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Celecoxib
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Cell Cycle / drug effects
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Cell Cycle Proteins / biosynthesis*
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Cell Line, Tumor
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Cell Survival / drug effects
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Cyclin-Dependent Kinase Inhibitor p27
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Cyclooxygenase 2
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Cyclooxygenase 2 Inhibitors
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Cyclooxygenase Inhibitors / pharmacology*
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Cyclooxygenase Inhibitors / therapeutic use
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Gene Expression Regulation, Neoplastic / drug effects
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Humans
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In Vitro Techniques
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Indomethacin / pharmacology
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Indomethacin / therapeutic use
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Isoenzymes / antagonists & inhibitors*
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Membrane Proteins
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Mouth Neoplasms / drug therapy*
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Mouth Neoplasms / metabolism
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Prostaglandin-Endoperoxide Synthases
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Pyrazoles
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S-Phase Kinase-Associated Proteins / biosynthesis*
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Sulfonamides / pharmacology
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Sulfonamides / therapeutic use
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Tumor Suppressor Protein p53 / biosynthesis
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Tumor Suppressor Proteins / biosynthesis*
Substances
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Cell Cycle Proteins
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Cyclooxygenase 2 Inhibitors
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Cyclooxygenase Inhibitors
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Isoenzymes
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Membrane Proteins
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Pyrazoles
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S-Phase Kinase-Associated Proteins
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Sulfonamides
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Tumor Suppressor Protein p53
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Tumor Suppressor Proteins
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Cyclin-Dependent Kinase Inhibitor p27
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Cyclooxygenase 2
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PTGS2 protein, human
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Prostaglandin-Endoperoxide Synthases
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Celecoxib
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Indomethacin