Telomere length in workers was effected by omethoate exposure and interaction between smoking and p 21 polymorphisms

J Environ Sci Health B. 2019;54(12):948-953. doi: 10.1080/03601234.2019.1652074. Epub 2019 Aug 12.

Abstract

Omethoate is an organophosphorus pesticide that poses a major health hazard, especially DNA damage. The purpose of this study was to investigate the factors affecting telomere length in workers exposed to omethoate by analyzing the interaction between cell cycle gene polymorphism and environmental factors. The exposure group consisted of 118 workers exposed to omethoate for 8-10 years, the control group comprised 115 healthy people without occupational toxicant exposure history. The telomere length of genomic DNA from peripheral blood leucocyte was determined with real-time PCR. Polymerase chain reaction and restriction fragment length polymorphism was used to detect the polymorphisms in p53, p21 and MDM2 gene. The telomere length in the (CA + AA) genotypes for p21 rs1801270 polymorphism was longer than that in the CC genotype in control group (P = 0.015). The generalized linear model analysis indicated the interaction of the p21 rs1801270 polymorphic (CA + AA) genotypes and smoking has a significant effect on telomere length (β = -0.258, P = 0.085). The prolongation of telomere length in omethoate-exposed workers was associated with genotypes (CA + AA) of p21 rs1801270, and interactions of (CA + AA) genotypes and smoking factor.

Keywords: Omethoate; cell cycle gene polymorphism; telomere length.

MeSH terms

  • Adult
  • DNA Damage / drug effects
  • Dimethoate / analogs & derivatives*
  • Dimethoate / toxicity
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Occupational Exposure / adverse effects*
  • Pesticides / toxicity*
  • Polymorphism, Genetic / drug effects
  • Proto-Oncogene Proteins c-mdm2 / genetics
  • Smoking / adverse effects*
  • Telomere / genetics
  • Telomere / metabolism*
  • Tumor Suppressor Protein p53 / genetics

Substances

  • Pesticides
  • Tumor Suppressor Protein p53
  • dimethoxon
  • MDM2 protein, human
  • Proto-Oncogene Proteins c-mdm2
  • Dimethoate