The polymorphisms in cGAS-STING pathway are associated with mitochondrial DNA copy number in coke oven workers

Int J Environ Health Res. 2023 Nov;33(11):1070-1080. doi: 10.1080/09603123.2022.2071418. Epub 2022 May 11.

Abstract

Objective: To evaluate the interaction effects of Polycyclic aromatic hydrocarbons (PAHs) exposure and variants in cGAS-STING genes on mitochondrial DNA copy number (mtDNAcn) in workers.

Methods: The mtDNAcn was determined by real-time quantitative polymerase-chain reaction in 544 PAHs-exposed workers and 238 office workers. The polymorphisms were detected by flight mass spectrometry.

Results: The mtDNAcn in PAHs exposure group was significantly lower than non-occupational exposure population (P < 0.00). The cGAS rs610913 CA+AA had significant interaction effects with STING rs11554776 GG+GA (P = 0.035), rs7380824 CC+CT (P = 0.026), and rs78233829 GC+CC (P = 0.034) on mtDNAcn. The generalized linear model results showed that the influencing factors of mtDNAcn include PAHs exposure (P < 0.001) and the interaction of PAHs exposure and cGAS rs 311678 AA+AG (P = 0.047).

Conclusion: The influencing factors of mtDNAcn include PAHs exposure and the interaction of PAHs exposure and cGAS rs 311678 AA+AG.

Keywords: Coke oven emissions; Mitochondrial DNA copy number; Polycyclic aromatic hydrocarbon; STING; cGAS rs311678.

MeSH terms

  • Coke* / adverse effects
  • DNA Copy Number Variations
  • DNA, Mitochondrial / genetics
  • Humans
  • Membrane Proteins* / genetics
  • Nucleotidyltransferases* / genetics
  • Occupational Exposure / adverse effects
  • Polycyclic Aromatic Hydrocarbons* / adverse effects

Substances

  • Coke
  • DNA, Mitochondrial
  • Nucleotidyltransferases
  • Polycyclic Aromatic Hydrocarbons
  • cGAS protein, human
  • STING1 protein, human
  • Membrane Proteins