Literature DB >> 24767943

The endogenous exposome.

Jun Nakamura1, Esra Mutlu1, Vyom Sharma1, Leonard Collins1, Wanda Bodnar1, Rui Yu1, Yongquan Lai1, Benjamin Moeller2, Kun Lu1, James Swenberg3.   

Abstract

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.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  DNA damage; Endogenous exposome; Mutagenesis; Risk assessment; Stable isotopes

Mesh:

Substances:

Year:  2014        PMID: 24767943      PMCID: PMC4097170          DOI: 10.1016/j.dnarep.2014.03.031

Source DB:  PubMed          Journal:  DNA Repair (Amst)        ISSN: 1568-7856


  139 in total

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Review 7.  DNA-protein crosslink formation by endogenous aldehydes and AP sites.

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