2016
DOI: 10.1016/j.etap.2016.06.001
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Sulfur mustard causes oxidants/antioxidants imbalance through the overexpression of free radical producing-related genes in human mustard lungs

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Cited by 17 publications
(8 citation statements)
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“…Eosinophils are a member of inflammatory response that are recruited to the damaged tissue and secret high levels of free radicals . Boskabady et al observed an increased number of eosinophils in lungs and BAL fluids of guinea pigs 14 days postexposure to SM. , Similarly, we have found overexpression of EPO in lungs of individuals who previously exposed to SM . However, the mechanism in which eosinophils are increased after SM exposure is unclear.…”
Section: Ros Producing-related Enzymessupporting
confidence: 64%
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“…Eosinophils are a member of inflammatory response that are recruited to the damaged tissue and secret high levels of free radicals . Boskabady et al observed an increased number of eosinophils in lungs and BAL fluids of guinea pigs 14 days postexposure to SM. , Similarly, we have found overexpression of EPO in lungs of individuals who previously exposed to SM . However, the mechanism in which eosinophils are increased after SM exposure is unclear.…”
Section: Ros Producing-related Enzymessupporting
confidence: 64%
“…Peroxiredoxins (Prdx) are a new class of thiol-specific antioxidants that protect cells from the action of H 2 O 2 in their reduced form. 64 Prdx antioxidative activity is dependent on cellular GSH content. Sulfiredoxin-1, which is a crucial oxidoreductase enzyme, catalyzes the reduction of cysteine sulfinic acid of hyperoxidized peroxiredoxins using ATP and GSH.…”
Section: ■ Glutathione Depletionmentioning
confidence: 99%
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“…Expression analyses of genes involved in oxidative stress and antioxidant defense in biopsies from 6 lungs of SM-exposed subjects (after 25 years from the event) revealed a disrupted expression pattern for more than eighty genes. In particular, the most upregulated genes were peroxiredoxins (PRDXS) and sulfiredoxin-1 (SRXN1) [ 29 ], oxidative stress responsive kinase-1 (OXSR1), forkhead box M1 (FOXM1), glutathione peroxidase-2 (GPX2) [ 30 ], and reactive oxygen species (ROS); in association with aldehyde oxidase 1 (AOX1), myeloperoxidase (MPO), dual oxidase 1 and 2 (DUOX1, DUOX2), thyroid peroxidase (TPO), and eosinophil peroxidase (EPO) [ 31 ]. On the other hand, the most downregulated genes were metallothionein-3 (MT3) and glutathione reductase (GSR).…”
Section: Sulfur Mustardmentioning
confidence: 99%