Expression of DNA repair genes in oral squamous cell carcinoma using reverse transcription-quantitative polymerase chain reaction

Oral Surg Oral Med Oral Pathol Oral Radiol. 2020 Sep;130(3):298-305. doi: 10.1016/j.oooo.2020.06.003. Epub 2020 Jun 10.

Abstract

Objective: The aim of this study was to evaluate the expression of DNA repair genes in cases of oral squamous cell carcinoma (OSCC).

Study design: Expression of the MLH1, MSH2, MLH3, ATM, MRE11A, XRCC1, and PMS2 genes was evaluated by reverse transcription-quantitative polymerase chain reaction in the OSCC group (32 patients) and the control group (15 patients). The groups were compared by using the Mann-Whitney test, with Bonferroni correction. Associations between gene expression levels and clinical data were explored by using Pearson's and Spearman's correlation coefficients, with P value less than .05 indicating a significant difference.

Results: The MLH1, MSH2, MLH3, ATM, MRE11A, XRCC1, and PMS2 genes were downregulated in the OSCC group compared with the control group, with significant values for MLH1 (P < .0001); MSH2 (P = .038); MLH3 (P < .0001); ATM (P < .0001); MRE11A (P < .0001); XRCC1 (P = .0004); and PMS2 (P = .008). Analysis of the correlation between gene expression and clinical data only revealed a significant negative correlation between age and expression of the PMS2 gene.

Conclusions: Expression of the DNA repair genes MLH1, MSH2, MLH3, ATM, MRE11 AMRE11A, XRCC1, and PMS2 was reduced in OSCC.

MeSH terms

  • Carcinoma, Squamous Cell* / genetics
  • DNA Repair / genetics
  • DNA Repair Enzymes / metabolism
  • Humans
  • Mismatch Repair Endonuclease PMS2
  • Mouth Neoplasms* / genetics
  • MutL Protein Homolog 1 / genetics
  • MutL Protein Homolog 1 / metabolism
  • Polymerase Chain Reaction
  • Reverse Transcription
  • X-ray Repair Cross Complementing Protein 1

Substances

  • X-ray Repair Cross Complementing Protein 1
  • XRCC1 protein, human
  • Mismatch Repair Endonuclease PMS2
  • MutL Protein Homolog 1
  • DNA Repair Enzymes