Promoter methylation of DAPK1, FHIT, MGMT, and CDKN2A genes in cervical carcinoma

Int J Clin Oncol. 2014 Feb;19(1):127-32. doi: 10.1007/s10147-013-0530-0. Epub 2013 Mar 14.

Abstract

Background and objectives: Aberrant DNA methylation contributes to the malignant phenotype in virtually all types of human cancer. This study explored the relationship between promoter methylation and inactivation of the DAPK1, FHIT, MGMT, and CDKN2A genes in cervical cancer.

Methods: The promoter methylation of DAPK1, FHIT, MGMT, and CDKN2A was investigated by using a methylation-specific polymerase chain reaction in 53 specimens of cervical cancer (42 squamous cell carcinoma, 11 adenocarcinoma), 22 specimens of intraepithelial neoplasia tissues, and 24 control normal cervical tissue specimens. The correlation of promoter methylation with the clinicopathological features of cervical cancer was analyzed. The expressions of DAPK1, FHIT, MGMT, and CDKN2A were detected by measuring relative mRNA levels.

Results: The promoter methylation of DAPK1, FHIT, MGMT, and CDKN2A in cervical cancer vs. intraepithelial neoplasia vs. normal cervical tissue was 75.5 vs. 31.8 vs. 4.2 % (p < 0.0001), 66.0 vs. 59.1 vs. 25.0 % (p = 0.0033), 34.0 vs. 27.3 vs. 20.8 % (p = 0.76), and 17.0 vs. 31.8 vs. 8.3 % (p = 0.11), respectively. The methylation of the promoter region significantly decreased the expression of only DAPK1 (p = 0.03). The methylation rate of the DAPK1 gene promoter was significantly higher in cervical cancer tissues than in cervical intraepithelial neoplasia and normal cervical tissues.

Conclusion: Promoter methylation may therefore lead to the inactivation of the DAPK1 gene, and may be related to the progression of cervical oncogenesis.

MeSH terms

  • Acid Anhydride Hydrolases / biosynthesis
  • Acid Anhydride Hydrolases / genetics*
  • Adult
  • Carcinoma in Situ / genetics
  • Carcinoma in Situ / pathology
  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / pathology
  • Cyclin-Dependent Kinase Inhibitor p16 / biosynthesis
  • Cyclin-Dependent Kinase Inhibitor p16 / genetics*
  • DNA Methylation / genetics
  • DNA Modification Methylases / biosynthesis
  • DNA Modification Methylases / genetics*
  • DNA Repair Enzymes / biosynthesis
  • DNA Repair Enzymes / genetics*
  • Death-Associated Protein Kinases / biosynthesis
  • Death-Associated Protein Kinases / genetics*
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Middle Aged
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Proteins / genetics*
  • Promoter Regions, Genetic
  • Tumor Suppressor Proteins / biosynthesis
  • Tumor Suppressor Proteins / genetics*
  • Uterine Cervical Neoplasms / genetics*
  • Uterine Cervical Neoplasms / pathology

Substances

  • Cyclin-Dependent Kinase Inhibitor p16
  • Neoplasm Proteins
  • Tumor Suppressor Proteins
  • fragile histidine triad protein
  • DNA Modification Methylases
  • MGMT protein, human
  • DAPK1 protein, human
  • Death-Associated Protein Kinases
  • Acid Anhydride Hydrolases
  • DNA Repair Enzymes