Department of Big Data in Health Science, School of Public Health and the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Unit of Cardiovascular and Nutritional Epidemiology, Institute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden.
EBioMedicine. 2024 May;103:105126. doi: 10.1016/j.ebiom.2024.105126. Epub 2024 Apr 16.
This study investigates the associations between air pollution and colorectal cancer (CRC) risk and survival from an epigenomic perspective.
Using a newly developed Air Pollutants Exposure Score (APES), we utilized a prospective cohort study (UK Biobank) to investigate the associations of individual and combined air pollution exposures with CRC incidence and survival, followed by an up-to-date systematic review with meta-analysis to verify the associations. In epigenetic two-sample Mendelian randomization analyses, we examine the associations between genetically predicted DNA methylation related to air pollution and CRC risk. Further genetic colocalization and gene-environment interaction analyses provided different insights to disentangle pathogenic effects of air pollution via epigenetic modification.
During a median 12.97-year follow-up, 5767 incident CRC cases among 428,632 participants free of baseline CRC and 533 deaths in 2401 patients with CRC were documented in the UK Biobank. A higher APES score was associated with an increased CRC risk (HR, 1.03, 95% CI = 1.01-1.06; P = 0.016) and poorer survival (HR, 1.13, 95% CI = 1.03-1.23; P = 0.010), particularly among participants with insufficient physical activity and ever smokers (P > 0.05). A subsequent meta-analysis of seven observational studies, including UK Biobank data, corroborated the association between PM exposure (per 10 μg/m increment) and elevated CRC risk (RR,1.42, 95% CI = 1.12-1.79; P = 0.004; I = 90.8%). Genetically predicted methylation at PM-related CpG site cg13835894 near TMBIM1/PNKD and cg16235962 near CXCR5, and NO-related cg16947394 near TMEM110 were associated with an increased CRC risk. Gene-environment interaction analysis confirmed the epigenetic modification of aforementioned CpG sites with CRC risk and survival.
Our study suggests the association between air pollution and CRC incidence and survival, underscoring the possible modifying roles of epigenomic factors. Methylation may partly mediate pathogenic effects of air pollution on CRC, with annotation to epigenetic alterations in protein-coding genes TMBIM1/PNKD, CXCR5 and TMEM110.
Xue Li is supported by the Natural Science Fund for Distinguished Young Scholars of Zhejiang Province (LR22H260001), the National Nature Science Foundation of China (No. 82204019) and Healthy Zhejiang One Million People Cohort (K-20230085). ET is supported by a Cancer Research UK Career Development Fellowship (C31250/A22804). MGD is supported by the MRC Human Genetics Unit Centre Grant (U127527198).
本研究从表观基因组学的角度探讨了空气污染与结直肠癌(CRC)风险和生存之间的关联。
我们使用新开发的空气污染暴露评分(APES),利用前瞻性队列研究(英国生物银行),研究个体和联合空气污染暴露与 CRC 发病和生存的关系,随后进行了最新的系统评价和荟萃分析,以验证这些关联。在表观遗传学两样本孟德尔随机化分析中,我们研究了与空气污染相关的 DNA 甲基化的遗传预测与 CRC 风险之间的关系。进一步的遗传共定位和基因-环境交互作用分析提供了不同的见解,以阐明通过表观遗传修饰的空气污染的致病作用。
在中位 12.97 年的随访期间,在英国生物银行中,428632 名无基线 CRC 的参与者中记录了 5767 例 CRC 发病病例,在 2401 例 CRC 患者中记录了 533 例死亡病例。APES 评分越高,CRC 风险越高(HR,1.03,95%CI=1.01-1.06;P=0.016),生存越差(HR,1.13,95%CI=1.03-1.23;P=0.010),尤其是在体力活动不足和曾经吸烟者中(P>0.05)。随后对包括英国生物银行数据在内的七项观察性研究的荟萃分析证实了 PM 暴露(每 10μg/m 增加)与 CRC 风险升高之间的关联(RR,1.42,95%CI=1.12-1.79;P=0.004;I=90.8%)。PM 相关 CpG 位点 cg13835894 附近的 TMBIM1/PNKD 和 cg16235962 附近的 CXCR5 以及与 NO 相关的 cg16947394 附近的 TMEM110 的基因预测甲基化与 CRC 风险增加有关。基因-环境交互作用分析证实了上述 CpG 位点与 CRC 风险和生存的表观遗传修饰。
我们的研究表明了空气污染与 CRC 发病和生存之间的关联,强调了表观基因组学因素的可能调节作用。甲基化可能部分介导了空气污染对 CRC 的致病作用,涉及到蛋白质编码基因 TMBIM1/PNKD、CXCR5 和 TMEM110 的表观遗传改变。
李雪得到了浙江省杰出青年自然科学基金(LR22H260001)、国家自然科学基金(No.82204019)和健康浙江百万人群队列(K-20230085)的支持。ET 得到了英国癌症研究协会职业发展奖学金(C31250/A22804)的支持。MGD 得到了 MRC 人类遗传学单位中心资助(U127527198)。