Abstract
In this study, the effects of HMBA on the expression of G0/G1 phase arrest-associated genes in human hepatocarcinoma SMMC-7721 cells were investigated. Immunocytochemistry and in situ hybridization assay revealed that the levels of p21WAF1/CIP1 and p16 proteins and the level of p21WAF1/CIP1 mRNA were increased while the levels of CDK4 and Cyclin D1 proteins and c-myc mRNA were decreased in the cells treated with HMBA. These results showed that HMBA could up-regulate the expression of p21WAF1/CIP1 and p16 genes, down-regulate the activity of Cyclin D1-CDK4 and the transcription of c-myc gene which were necessary for cells entering into S phase, and so arrest the cells in G0/G1 phase, and induce the differentiation of human hepatocarcinoma SMMC-7721 cells.
MeSH terms
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Acetamides / pharmacology*
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Carcinoma, Hepatocellular / metabolism*
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Cell Cycle Proteins / genetics
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Cell Cycle Proteins / metabolism*
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Cell Differentiation / drug effects
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Cell Differentiation / genetics
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Cell Line, Tumor
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Cyclin D1 / metabolism
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Cyclin-Dependent Kinase 4 / metabolism
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Cyclin-Dependent Kinase Inhibitor p16
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Cyclin-Dependent Kinase Inhibitor p21 / genetics
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Cyclin-Dependent Kinase Inhibitor p21 / metabolism*
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Gene Expression / drug effects
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Humans
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Immunohistochemistry
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In Situ Hybridization
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Liver Neoplasms / metabolism*
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Neoplasm Proteins / metabolism
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Proto-Oncogene Proteins c-myc / genetics
Substances
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Acetamides
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CDKN1A protein, human
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CDKN2A protein, human
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Cell Cycle Proteins
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Cyclin-Dependent Kinase Inhibitor p16
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Cyclin-Dependent Kinase Inhibitor p21
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MYC protein, human
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Neoplasm Proteins
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Proto-Oncogene Proteins c-myc
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Cyclin D1
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Cyclin-Dependent Kinase 4
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hexamethylene bisacetamide