Quantitative analysis of the level of p53 and p21(WAF1) mRNA in human colon cancer HT-29 cells treated with inositol hexaphosphate.

Abstract

The aim of this study was to analyze the molecular mechanism of inositol hexaphosphate (InsP(6)) action through which it may inhibit proliferation of colon cancer cells and cell cycle progression. A kinetic study of p53 and p21(WAF1) mRNA increase was performed on human colon cancer HT-29 cells after treatment with 1, 5 and 10 mM InsP(6) for 6, 12, 24 and 48 h. Real-time-QPCR based on TaqMan methodology was applied to analyze quantitatively the transcript levels of these genes. The transcription of beta-actin and GAPDH genes was assessed in parallel to select the control gene with least variability. The 2(-Delta Delta Ct) method was used to analyze the relative changes in gene transcription. InsP(6) stimulated p53 and p21(WAF1) expression at the mRNA level, with the highest increase in p21(WAF1) mRNA occurring at 24 h, i.e., following the highest increase in p53 mRNA observed at 12 h. Based on these studies it may be concluded that the ability of InsP(6) to arrest the cell cycle may be mediated by the transcriptional up-regulation of the p53-responsive p21(WAF1) gene.

• Authors: Ludmiła Weglarz, Izabela Molin, Arkadiusz Orchel, Beata Parfiniewicz, Zofia Dzierzewicz
• Journal: Acta biochimica Polonica (Acta Biochim Pol) Vol. 53 Issue 2 Pg. 349-56 ( 2006) ISSN: 0001-527X [Print] Poland
• PMID: 16733561 (Publication Type: Journal Article)

Chemical References

• Antineoplastic Agents
• Cyclin-Dependent Kinase Inhibitor p21
• RNA, Messenger
• Phytic Acid

Topics

• Antineoplastic Agents (pharmacology)
• Cyclin-Dependent Kinase Inhibitor p21 (genetics)
• Gene Expression Regulation, Neoplastic (drug effects)
• Genes, p53 (genetics)
• HT29 Cells
• Humans
• Phytic Acid (pharmacology)
• RNA, Messenger (genetics, metabolism)
• Reverse Transcriptase Polymerase Chain Reaction (methods)
• Time Factors
• Transcription, Genetic (drug effects)