Abstract
Although smoking and oxidative stress are known contributors to lung carcinogenesis, their mechanisms of action remain poorly understood. To shed light into these mechanisms, we applied a novel approach using Cys34-adductomics in a lung cancer nested case–control study (n = 212). Adductomics profiles were integrated with DNA-methylation data at established smoking-related CpG sites measured in the same individuals. Our analysis identified 42 Cys34-albumin adducts, of which 2 were significantly differentially abundant in cases and controls: adduct of N-acetylcysteine (NAC, p = 4.15 × 10−3) and of cysteinyl-glycine (p = 7.89 × 10−3). Blood levels of the former were found associated to the methylation levels at 11 smoking-related CpG sites. We detect, for the first time in prospective blood samples, and irrespective of time to diagnosis, decreased levels of NAC adduct in lung cancer cases. Altogether, our results highlight the potential role of these adducts in the oxidative stress response contributing to lung carcinogenesis years before diagnosis.
| Original language | English |
|---|---|
| Pages (from-to) | 3294-3303 |
| Number of pages | 10 |
| Journal | International Journal of Cancer |
| Volume | 146 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 15 Jun 2020 |
Bibliographical note
Cited By :4Export Date: 8 December 2021
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- adductomics
- lung cancer
- DNA-methylation
- biomarkers
- oxidative stress
- smoking
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