Iron induced RNA-oxidation in the general population and in mouse tissue

TY - JOUR

T1 - Iron induced RNA-oxidation in the general population and in mouse tissue

AU - Cejvanovic, Vanja

AU - Kjær, Laura Kofoed

AU - Bergholdt, Helle Kirstine Mørup

AU - Torp-Pedersen, Arendse

AU - Henriksen, Trine

AU - Weimann, Allan

AU - Ellervik, Christina

AU - Poulsen, Henrik Enghusen

PY - 2018

Y1 - 2018

N2 - Iron promotes formation of hydroxyl radicals by the Fenton reaction, subsequently leading to potential oxidatively generated damage of nucleic acids. Oxidatively generated damage to RNA, measured as 8-oxo-7,8-dihydroguanosine (8-oxoGuo) in urine, is increased in patients with genetic iron overload, which have led us to test the hypothesis that high iron status, assessed by iron biomarkers and genetic disposition, increases urinary excretion of 8-oxoGuo. In a general Danish population study we used a Mendelian randomization design with HFE genotypes as a proxy for iron status and supplemented with ex vivo experiments in mice muscle tissue exposed to iron(II) sulfate to attempt to clarify this hypothesis. The biomarkers ferritin, transferrin, and transferrin saturation (TS) were associated with 8-oxoGuo (in linear univariable and multivariable regression analyses: P < 0.001). Mendelian randomization indicated a causal pathway between genetically elevated iron biomarkers (assessed by ferritin and TS) and high levels of 8-oxoGuo. The ex vivo experiments showed a monotonically increase in 8-oxoGuo with increased iron concentration (ANOVA: P = 0.0008) that was prevented with iron chelation (P = 0.01). Our results indicate a causal relationship between iron biomarkers and 8-oxoGuo. Furthermore, the ex vivo experiment shows a mechanistic link between iron and 8-oxoGuo formation. Both iron overload and the biomarker 8-oxoGuo have been linked to e.g. diabetes, which merits future studies to investigate if iron induced 8-oxoGuo is involved in disease development.

AB - Iron promotes formation of hydroxyl radicals by the Fenton reaction, subsequently leading to potential oxidatively generated damage of nucleic acids. Oxidatively generated damage to RNA, measured as 8-oxo-7,8-dihydroguanosine (8-oxoGuo) in urine, is increased in patients with genetic iron overload, which have led us to test the hypothesis that high iron status, assessed by iron biomarkers and genetic disposition, increases urinary excretion of 8-oxoGuo. In a general Danish population study we used a Mendelian randomization design with HFE genotypes as a proxy for iron status and supplemented with ex vivo experiments in mice muscle tissue exposed to iron(II) sulfate to attempt to clarify this hypothesis. The biomarkers ferritin, transferrin, and transferrin saturation (TS) were associated with 8-oxoGuo (in linear univariable and multivariable regression analyses: P < 0.001). Mendelian randomization indicated a causal pathway between genetically elevated iron biomarkers (assessed by ferritin and TS) and high levels of 8-oxoGuo. The ex vivo experiments showed a monotonically increase in 8-oxoGuo with increased iron concentration (ANOVA: P = 0.0008) that was prevented with iron chelation (P = 0.01). Our results indicate a causal relationship between iron biomarkers and 8-oxoGuo. Furthermore, the ex vivo experiment shows a mechanistic link between iron and 8-oxoGuo formation. Both iron overload and the biomarker 8-oxoGuo have been linked to e.g. diabetes, which merits future studies to investigate if iron induced 8-oxoGuo is involved in disease development.

KW - 8-dihydro-2′-deoxyguanosine

KW - 8-dihydroguanosine

KW - 8-hydroxy-2′-deoxyguanosine

KW - 8-hydroxyguanosine

KW - 8-oxo-7

KW - C282Y

KW - Ferritin

KW - H63D

KW - Hemochromatosis

KW - HFE

KW - Instrumental variable analysis

KW - Iron

KW - Iron overload

KW - Mendelian randomization

KW - Oxidative stress

KW - Transferrin

KW - Transferrin saturation

U2 - 10.1016/j.freeradbiomed.2017.11.013

DO - 10.1016/j.freeradbiomed.2017.11.013

M3 - Journal article

C2 - 29157668

AN - SCOPUS:85036558601

SN - 0891-5849

VL - 115

SP - 127

EP - 135

JO - Free Radical Biology & Medicine

JF - Free Radical Biology & Medicine

ER -