Nakamura Jun, Mutlu Esra, Sharma Vyom, Collins Leonard, Bodnar Wanda, Yu Rui, Lai Yongquan, Moeller Benjamin, Lu Kun, Swenberg James
University of North Carolina, Chapel Hill, NC, United States.
University of North Carolina, Chapel Hill, NC, United States; Lovelace Respiratory Research Institute, Albuquerque, NM, United States.
DNA Repair (Amst). 2014 Jul;19:3-13. doi: 10.1016/j.dnarep.2014.03.031. Epub 2014 Apr 24.
The concept of the Exposome is a compilation of diseases and one's lifetime exposure to chemicals, whether the exposure comes from environmental, dietary, or occupational exposures; or endogenous chemicals that are formed from normal metabolism, inflammation, oxidative stress, lipid peroxidation, infections, and other natural metabolic processes such as alteration of the gut microbiome. In this review, we have focused on the endogenous exposome, the DNA damage that arises from the production of endogenous electrophilic molecules in our cells. It provides quantitative data on endogenous DNA damage and its relationship to mutagenesis, with emphasis on when exogenous chemical exposures that produce identical DNA adducts to those arising from normal metabolism cause significant increases in total identical DNA adducts. We have utilized stable isotope labeled chemical exposures of animals and cells, so that accurate relationships between endogenous and exogenous exposures can be determined. Advances in mass spectrometry have vastly increased both the sensitivity and accuracy of such studies. Furthermore, we have clear evidence of which sources of exposure drive low dose biology that results in mutations and disease. These data provide much needed information to impact quantitative risk assessments, in the hope of moving towards the use of science, rather than default assumptions.
暴露组的概念是对疾病以及个体一生中接触化学物质情况的汇总,无论这种接触是来自环境、饮食还是职业暴露;或者是由正常代谢、炎症、氧化应激、脂质过氧化、感染以及其他自然代谢过程(如肠道微生物群改变)所形成的内源性化学物质。在本综述中,我们聚焦于内源性暴露组,即我们细胞内产生内源性亲电分子所引发的DNA损伤。它提供了关于内源性DNA损伤及其与诱变关系的定量数据,重点关注产生与正常代谢产生的相同DNA加合物的外源性化学暴露何时会导致总相同DNA加合物显著增加。我们利用了对动物和细胞进行稳定同位素标记的化学暴露,以便能够确定内源性和外源性暴露之间的准确关系。质谱技术的进步极大地提高了此类研究的灵敏度和准确性。此外,我们有明确的证据表明哪些暴露源驱动了导致突变和疾病的低剂量生物学效应。这些数据为影响定量风险评估提供了急需的信息,以期朝着运用科学而非默认假设的方向发展。