This is a minor acrolein-derived deoxyguanosine adduct discussed as a distinct lesion with mutagenic behavior. The review contrasts it with gamma-HOPdG because the two adducts behave differently in mutagenicity.
First-pass extracted concept
alpha-hydroxy-1,N(2)-propano-2'-deoxyguanosine
Aliases
alpha-HOPdG, alpha-OH-PdG
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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.
Alpha-HOPdG is mutagenic in both in vitro and in vivo test systems and may accumulate in vivo because it is difficult to repair.