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Genetic damage and potential mechanism exploration under different air pollution patterns by multi-omics.
Xu, Jiayu; Zhang, Qiaojian; Su, Zekang; Liu, Yu; Yan, Tenglong; Zhang, Yali; Wang, Tiancheng; Wei, Xuetao; Chen, Zhangjian; Hu, Guiping; Chen, Tian; Jia, Guang.
Afiliación
  • Xu J; Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100083, China.
  • Zhang Q; Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100083, China.
  • Su Z; Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100083, China.
  • Liu Y; Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100083, China.
  • Yan T; Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100083, China.
  • Zhang Y; Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100083, China.
  • Wang T; Department of Clinical Laboratory, Third Hospital of Peking University, Beijing 100083, China.
  • Wei X; Department of Toxicology, School of Public Health, Peking University, Beijing 100083, China.
  • Chen Z; Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100083, China.
  • Hu G; School of Medical Science and Engineering, Beihang University, Beijing 100191, China.
  • Chen T; School of Public Health and Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, China.
  • Jia G; Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100083, China. Electronic address: jiaguangjia@bjmu.edu.cn.
Environ Int ; 170: 107636, 2022 12.
Article en En | MEDLINE | ID: mdl-36423397
Ambient air pollution was classified as carcinogenic to humans (Group 1) for lung cancer. DNA damage was an important first step in the process of carcinogenesis, and could also be induced by air pollution. In this study, intratracheal instillation and real-time air exposure system were combined to establish SHP (short-term high-level PM2.5) and LLPO (long-term low-level PM2.5 and O3) exposure patterns, respectively. Hierarchical levels of genetic biomarkers were analyzed to explore DNA damage effects in rats. Representative DNA repair genes from different repair pathways were selected to explore the relative expression levels. The methylation level of differentially expressed repair genes were also determined. Besides, miRNA sequencing and non-targeted metabolomic analysis were performed in rat lungs. KEGG and multi-omics analysis were used to explore the potential mechanism of genetic damage under different air pollution patterns. We found that LLPO exposure induced DSBs and chromosome damage. SHP exposure could induce DSBs and DNA oxidative damage, and the effects of genetic damage under this pollution pattern could be repaired by natural repair. Repair genes involved in two pattern were different. SHP exposure could induce higher methylation levels of RAD51, which might be a potential epigenetic mechanism for high-level PM2.5 induced down-regulated expression of RAD51 and DSBs. Besides, 29 overlapped alterations in metabolic pathways were identified by metabolomic and miRNA sequencing, including purine metabolism and pyrimidine metabolism after LLPO exposure. Differential miRNAs expression in lung tissue were associated with apoptosis, DNA damage and damage repair. We concluded that under different air pollution patterns, DNA damage biomarkers and activated targets of DNA damage repair network were both different. The genetic damage effects caused by high-level short-term PM2.5 can be alleviated by natural repair. We provided possible mechanisms by multi-omics which could explain the increased carcinogenic risk caused by air pollution.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: MicroARNs / Enzimas Reparadoras del ADN / Contaminación del Aire / Exposición a Riesgos Ambientales / Material Particulado / Roturas del ADN de Doble Cadena / Carcinogénesis Límite: Animals / Humans Idioma: En Revista: Environ Int Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: MicroARNs / Enzimas Reparadoras del ADN / Contaminación del Aire / Exposición a Riesgos Ambientales / Material Particulado / Roturas del ADN de Doble Cadena / Carcinogénesis Límite: Animals / Humans Idioma: En Revista: Environ Int Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos