Inhibition by Tetrahydroquinoline Sulfonamide Derivatives of the Activity of Human 8-Oxoguanine DNA Glycosylase (OGG1) for Several Products of Oxidatively induced DNA Base Lesions.
Melis KantYu-Ki TaharaPawel JarugaErdem CoskunR Stephen LloydEric T KoolMiral DizdarogluPublished in: ACS chemical biology (2020)
DNA glycosylases involved in the first step of the DNA base excision repair pathway are promising targets in cancer therapy. There is evidence that reduction of their activities may enhance cell killing in malignant tumors. Recently, two tetrahydroquinoline compounds named SU0268 and SU0383 were reported to inhibit OGG1 for the excision of 8-hydroxyguanine. This DNA repair protein is one of the major cellular enzymes responsible for excision of a number of oxidatively induced lesions from DNA. In this work, we used gas chromatography-tandem mass spectrometry with isotope-dilution to measure the excision of not only 8-hydroxyguanine but also that of the other major substrate of OGG1, i.e., 2,6-diamino-4-hydroxy-5-formamidopyrimidine, using genomic DNA with multiple purine- and pyrimidine-derived lesions. The excision of a minor substrate 4,6-diamino-5-formamidopyrimidine was also measured. Both SU0268 and SU0383 efficiently inhibited OGG1 activity for these three lesions, with the former being more potent than the latter. Dependence of inhibition on concentrations of SU0268 and SU0383 from 0.05 μmol/L to 10 μmol/L was also demonstrated. The approach used in this work may be applied to the investigation of OGG1 inhibition by SU0268 and SU0383 and other small molecule inhibitors in further studies including cellular and animal models of disease.
Keyphrases
- dna repair
- circulating tumor
- gas chromatography
- tandem mass spectrometry
- cell free
- dna damage
- single molecule
- small molecule
- mass spectrometry
- ultra high performance liquid chromatography
- dna damage response
- liquid chromatography
- cancer therapy
- nucleic acid
- high performance liquid chromatography
- circulating tumor cells
- high resolution mass spectrometry
- endothelial cells
- high resolution
- solid phase extraction
- drug delivery
- bone marrow
- stem cells
- oxidative stress
- gene expression
- single cell
- cell therapy
- drug induced
- structure activity relationship