Inhibition of human APE1 and MTH1 DNA repair proteins by dextran-coated γ-Fe 2 O 3 ultrasmall superparamagnetic iron oxide nanoparticles.
Erdem CoskunNeenu SinghLeona D ScanlanPawel JarugaShareen H DoakMiral DizdarogluBryant C NelsonPublished in: Nanomedicine (London, England) (2023)
Aim: To quantitatively evaluate the inhibition of human DNA repair proteins APE1 and MTH1 by dextran-coated γ-Fe 2 O 3 ultrasmall superparamagnetic iron oxide nanoparticles (dUSPIONs). Materials & methods : Liquid chromatography-tandem mass spectrometry with isotope-dilution was used to measure the expression levels of APE1 and MTH1 in MCL-5 cells exposed to increasing doses of dUSPIONs. The expression levels of APE1 and MTH1 were measured in cytoplasmic and nuclear fractions of cell extracts. Results: APE1 and MTH1 expression was significantly inhibited in both cell fractions at the highest dUSPION dose. The expression of MTH1 was linearly inhibited across the full dUSPION dose range in both fractions. Conclusion: These findings warrant further studies to characterize the capacity of dUSPIONs to inhibit other DNA repair proteins in vitro and in vivo .
Keyphrases
- dna repair
- iron oxide nanoparticles
- dna damage
- poor prognosis
- liquid chromatography tandem mass spectrometry
- dna damage response
- endothelial cells
- single cell
- long non coding rna
- simultaneous determination
- stem cells
- induced apoptosis
- iron oxide
- oxidative stress
- solid phase extraction
- bone marrow
- cell proliferation
- high resolution
- endoplasmic reticulum stress
- mass spectrometry