Nicotine exposure augments renal toxicity of 5-azacytidine through p66shc: Prevention by resveratrol

Abstract

Background/Aim: We have shown that either chronic nicotine (NIC) exposure or 5-aza-cytidine (AZA) augments oxidative stress-dependent injury through stimulating p66shc in renal cells. Hence, NIC could exacerbate adverse effects of AZA while antioxidants such as resveratrol (RES) could prevent it. Materials and Methods: Renal proximal tubule cells (NRK52E) were treated with 20 M RES prior to 200 M NIC plus 100 nM AZA and cell injury (LDH release) was determined. Reporter luciferase assays determined p66shc activation and RES-induced antioxidant responses. Genetic manipulations identified the mechanism of RES action. Results: NIC exacerbated AZAdependent injury via augmenting p66shc transcription. While RES suppressed NIC+AZA-mediated injury,-surprisingly-it further enhanced activity of the p66shc promoter. RES protected cells via the cytoplasmic p66shc/Nrf2/heme oxygenase-1 (HO-1) axis. Conclusion: RES can protect the kidney from adverse effects of NIC in patients undergoing anticancer therapy.