Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing, 100083, China.
Department of Laboratory Animal Science, Health Science Center, Peking University, Beijing, 100083, China.
Environ Pollut. 2022 Mar 15;297:118763. doi: 10.1016/j.envpol.2021.118763. Epub 2022 Jan 5.
Outdoor air pollution has been classified as carcinogenic to humans (Group 1) for lung cancer, but the underlying mechanism and key toxic components remain incompletely understood. Since DNA damage and metabolite alterations are associated with cancer progression, exploring potential mechanisms linking air pollution and cancer might be meaningful. In this study, a real-time ambient air exposure system was established to simulate the real-world environment of adult male SD rats in Beijing from June 13th, 2018, to October 8th, 2018. 8-OHdG in the urine, γ-H2AX in the lungs and mtDNA copy number in the peripheral blood were analyzed to explore DNA damage at different levels. Serum non-targeted metabolomics analysis was performed. Pair-wise spearman was used to explore the correlation between DNA damage biomarkers and serum differential metabolites. Carcinogenic risks of heavy metals and PAHs via inhalation were assessed according to US EPA guidelines. Results showed that PM and O were the major air pollutants in the exposure group and not detected in the control group. Compared with control group, higher levels of 8-OHdG, mtDNA copy number, γ-H2AX and PCNA-positive nuclei cells were observed in the exposure group. Histopathological evaluation suggested ambient air induced alveolar wall thickening and inflammatory cell infiltration in lungs. Perturbed metabolic pathways identified included glycolysis/gluconeogenesis metabolism, purine and pyrimidine metabolism, etc. γ-H2AX was positively correlated with serum ADP, 3-phospho-D-glyceroyl phosphate and N-acetyl-D-glucosamine. The BaPeq was 0.120 ng/m. Risks of Cr(VI), As, V, BaP, BaA and BbF were above 1 × 10. We concluded that low-level air pollution was associated with DNA damage and serum metabolomic alterations in rats. Cr(VI) and BaP were identified as key carcinogenic components in PM. Our results provided experimental evidence for hazard identification and risk assessment of low-level air pollution.
室外空气污染已被归类为肺癌的人类致癌物质(第 1 组),但潜在机制和关键有毒成分仍不完全清楚。由于 DNA 损伤和代谢物改变与癌症进展有关,因此探索空气污染与癌症之间潜在的联系机制可能具有重要意义。在这项研究中,建立了一个实时环境空气暴露系统,以模拟 2018 年 6 月 13 日至 2018 年 10 月 8 日期间北京成年雄性 SD 大鼠的真实环境。分析尿液中的 8-OHdG、肺部中的 γ-H2AX 和外周血中的 mtDNA 拷贝数,以探讨不同水平的 DNA 损伤。进行了血清非靶向代谢组学分析。使用两两 spearman 分析探索 DNA 损伤生物标志物与血清差异代谢物之间的相关性。根据美国环保署指南评估重金属和 PAHs 通过吸入的致癌风险。结果表明,PM 和 O 是暴露组中的主要空气污染物,而在对照组中未检测到。与对照组相比,暴露组中 8-OHdG、mtDNA 拷贝数、γ-H2AX 和 PCNA 阳性核细胞的水平更高。组织病理学评估表明,环境空气引起了肺部肺泡壁增厚和炎症细胞浸润。鉴定出的失调代谢途径包括糖酵解/糖异生代谢、嘌呤和嘧啶代谢等。γ-H2AX 与血清 ADP、3-磷酸-D-甘油酸和 N-乙酰-D-葡萄糖胺呈正相关。BaPeq 为 0.120ng/m。Cr(VI)、As、V、BaP、BaA 和 BbF 的风险均高于 1×10。我们得出结论,低水平空气污染与大鼠的 DNA 损伤和血清代谢组学改变有关。Cr(VI)和 BaP 被确定为 PM 中的关键致癌成分。我们的结果为低水平空气污染的危害识别和风险评估提供了实验证据。