This is the major acrolein-derived deoxyguanosine adduct highlighted by the review. It is linked to interstrand DNA-DNA and DNA-peptide/protein cross-links that may contribute to mutagenicity.
First-pass extracted concept
gamma-hydroxy-1,N(2)-propano-2'-deoxyguanosine
Aliases
gamma-HOPdG, gamma-OH-PdG
Extracted Explainers
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Evidence Snippets
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Linked Claims
Alpha-HOPdG and gamma-HOPdG differ in mutagenic behavior, with gamma-HOPdG being the major adduct and alpha-HOPdG being less abundant but harder to repair.
Inconsistent results in acrolein mutagenicity studies are attributed at least partly to formation of multiple acrolein-DNA adducts and their differential repair in diverse detection systems.
Detection of acrolein-DNA adducts in human lung tissues and analysis of p53 mutation spectra in acrolein-treated cells may inform mechanisms of acrolein mutagenicity.
Acrolein mutagenicity relies on formation of DNA adducts.
Gamma-HOPdG can generate interstrand DNA-DNA and DNA-peptide/protein cross-links that may contribute to mutagenicity, but repair by some DNA polymerase complexes can lessen its mutagenic effects.