Scholl P, Musser S M, Kensler T W, Groopman J D
Johns Hopkins University, School of Hygiene and Public Health, Department of Environmental Health Sciences, Baltimore, MD 21205, USA.
Pharmacogenetics. 1995;5 Spec No:S171-6. doi: 10.1097/00008571-199512001-00022.
The rationale for developing molecular biomarkers to monitor and assess risk from human exposure to aflatoxins have been justified by the association of these carcinogens with human liver cancer, a disease that causes at least 250000 deaths world-wide each year. The goal of our research has been the development of aflatoxin biomarkers based upon the knowledge of the biochemistry and toxicology of aflatoxins gleaned from both experimental and human studies. These biomarkers have been subsequently utilized in experimental chemoprotection models to provide data on the modulation of these markers under different situations of disease risk. Several of the aflatoxin specific biomarkers have been validated in epidemiologic studies and are now available to use as intermediate biomarkers in chemoprotection trials. This systematic approach provides encouragement for preventive interventions and should serve as a template for the development, validation and application of other chemical-specific biomarkers to cancer or other chronic diseases.
开发分子生物标志物以监测和评估人类接触黄曲霉毒素的风险,其理论依据是这些致癌物与人类肝癌之间的关联。肝癌是一种每年在全球至少导致25万人死亡的疾病。我们的研究目标是,基于从实验研究和人体研究中收集到的黄曲霉毒素生物化学和毒理学知识,开发黄曲霉毒素生物标志物。这些生物标志物随后被用于实验性化学预防模型,以提供在不同疾病风险情况下这些标志物调节情况的数据。几种黄曲霉毒素特异性生物标志物已在流行病学研究中得到验证,现在可作为化学预防试验中的中间生物标志物使用。这种系统方法为预防性干预提供了支持,应作为开发、验证和应用其他针对癌症或其他慢性病的化学特异性生物标志物的模板。