Young Anna S, Mullins Catherine E, Sehgal Neha, Vermeulen Roel C H, Kolijn P Martijn, Vlaanderen Jelle, Rahman Mohammad L, Birmann Brenda M, Barupal Dinesh, Lan Qing, Rothman Nathaniel, Walker Douglas I
Gangarosa Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, GA 30322, United States.
Institute for Risk Assessment Sciences, Utrecht University, Utrecht 3584 CM, The Netherlands.
JNCI Cancer Spectr. 2025 Jan 3;9(1). doi: 10.1093/jncics/pkae122.
Despite advances in understanding genetic susceptibility to cancer, much of cancer heritability remains unidentified. At the same time, the makeup of industrial chemicals in our environment only grows more complex. This gap in knowledge on cancer risk has prompted calls to expand cancer research to the comprehensive, discovery-based study of nongenetic environmental influences, conceptualized as the "exposome."
Our scoping review aimed to describe the exposome and its application to cancer epidemiology and to study design limitations, challenges in analytical methods, and major unmet opportunities in advanced exposome profiling methods that allow the quantification of complex chemical exposure profiles in biological matrices. To evaluate progress on incorporating measurements of the exposome into cancer research, we performed a review of such "cancer exposome" studies published through August 2023.
We found that only 1 study leveraged untargeted chemical profiling of the exposome as a method to measure tens of thousands of environmental chemicals and identify prospective associations with future cancer risk. The other 13 studies used hypothesis-driven exposome approaches that targeted a set of preselected lifestyle, occupational, air quality, social determinant, or other external risk factors. Many of the included studies could only leverage sample sizes with less than 400 cancer cases (67% of nonecologic studies) and exposures experienced after diagnosis (29% of studies). Six cancer types were covered, most commonly blood (43%), lung (21%), or breast (14%) cancer.
The exposome is underutilized in cancer research, despite its potential to unravel complex relationships between environmental exposures and cancer and to inform primary prevention.
尽管在了解癌症遗传易感性方面取得了进展,但许多癌症遗传性仍未明确。与此同时,我们环境中工业化学品的构成只会变得更加复杂。癌症风险知识方面的这一差距促使人们呼吁将癌症研究扩展到对非遗传环境影响的全面、基于发现的研究,即概念化为“暴露组”的研究。
我们的范围综述旨在描述暴露组及其在癌症流行病学中的应用,并研究设计局限性、分析方法中的挑战以及先进暴露组分析方法中的主要未满足机会,这些方法能够量化生物基质中的复杂化学暴露谱。为了评估将暴露组测量纳入癌症研究的进展情况,我们对截至2023年8月发表的此类“癌症暴露组”研究进行了综述。
我们发现,只有1项研究利用暴露组的非靶向化学分析作为一种方法来测量数以万计的环境化学品,并确定与未来癌症风险的前瞻性关联。其他13项研究采用了假设驱动的暴露组方法,这些方法针对一组预先选定的生活方式、职业、空气质量、社会决定因素或其他外部风险因素。许多纳入研究只能利用样本量少于400例癌症病例的样本(67%的非生态学研究)以及诊断后经历的暴露(29%的研究)。涵盖了六种癌症类型,最常见的是血液癌(43%)、肺癌(21%)或乳腺癌(14%)。
暴露组在癌症研究中的利用不足,尽管其有潜力揭示环境暴露与癌症之间的复杂关系并为一级预防提供信息。