Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:8565117rdf:typepubmed:Citationlld:pubmed
pubmed-article:8565117lifeskim:mentionsumls-concept:C1003377lld:lifeskim
pubmed-article:8565117lifeskim:mentionsumls-concept:C0017108lld:lifeskim
pubmed-article:8565117lifeskim:mentionsumls-concept:C0012854lld:lifeskim
pubmed-article:8565117lifeskim:mentionsumls-concept:C0020281lld:lifeskim
pubmed-article:8565117lifeskim:mentionsumls-concept:C0199176lld:lifeskim
pubmed-article:8565117lifeskim:mentionsumls-concept:C0050078lld:lifeskim
pubmed-article:8565117lifeskim:mentionsumls-concept:C0205263lld:lifeskim
pubmed-article:8565117lifeskim:mentionsumls-concept:C2700605lld:lifeskim
pubmed-article:8565117pubmed:issue1lld:pubmed
pubmed-article:8565117pubmed:dateCreated1996-3-1lld:pubmed
pubmed-article:8565117pubmed:abstractTextThe capability of Cr(III) to induce DNA lesions generated by oxidative damage was investigated in this study by examining the formation of 8-hydroxydeoxyguanosine (8-OHdG) in calf thymus DNA by CrCl3 and/or H2O2 in 10 mM phosphate buffer. In the presence of 0.5 mM H2O2, the formation of 8-OHdG markedly increased with increasing CrCl3 concentration. In contrast, H2O2 or CrCl3 alone did not cause any increase in 8-OHdG level above background. The amount of 8-OHdG induced by CrCl3 plus H2O2 was time dependent; its generation increased linearly over an incubation period of 90 min. The formation of 8-OHdG was unfavorable in an acidic solution (pH < 6); the highest level of 8-OHdG was observed at pH 7-8. Scavengers of reactive oxygen species markedly inhibited the formation of 8-OHdG by CrCl3 plus H2O2; the inhibition effect was sodium azide > D-mannitol > Tris-HCl at an equal concentration. The induction of 8-OHdG by CrCl3 plus H2O2 remained unchanged in D2O. Moreover, an addition of catalase (2.2 U/ml) to the reaction mixture completely inhibited the formation of 8-OHdG by CrCl3/H2O2, whereas only 22% of that formation was inhibited by superoxide dismutase (11 U/ml). A large amount of bovine serum albumin (1.1 mg/ml) could reduce the formation of 8-OHdG by CrCl3 plus H2O2, thereby implying that Cr(III)-mediated DNA-protein crosslinks are unfavorable for 8-OHdG formation. Furthermore, ascorbate could prevent the formation of 8-OHdG by CrCl3 plus H2O2; the extent of prevention increased with increasing ascorbate concentration (10 microM-3 mM). Thus, ascorbate acts as a free radical scavenger in the CrCl3/H2O2 system. The above findings suggest that Cr(III)/H2O2 could generate oxidative damage to DNA, possibly through a Fenton-like reaction, i.e. Cr(III)+H2O2-->Cr(IV)+.OH+OH-. This study also indicates that Cr(III), previously considered as the ultimate kinetically stable species of Cr(VI) metabolites, is capable of inducing carcinogenic lesions through interaction with a cellular oxygen species.lld:pubmed
pubmed-article:8565117pubmed:languageenglld:pubmed
pubmed-article:8565117pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8565117pubmed:citationSubsetIMlld:pubmed
pubmed-article:8565117pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8565117pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8565117pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8565117pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8565117pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8565117pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8565117pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8565117pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8565117pubmed:statusMEDLINElld:pubmed
pubmed-article:8565117pubmed:monthJanlld:pubmed
pubmed-article:8565117pubmed:issn0143-3334lld:pubmed
pubmed-article:8565117pubmed:authorpubmed-author:ChenC LCLlld:pubmed
pubmed-article:8565117pubmed:authorpubmed-author:KAUQ YQYlld:pubmed
pubmed-article:8565117pubmed:authorpubmed-author:YangJ LJLlld:pubmed
pubmed-article:8565117pubmed:authorpubmed-author:TsouT CTClld:pubmed
pubmed-article:8565117pubmed:issnTypePrintlld:pubmed
pubmed-article:8565117pubmed:volume17lld:pubmed
pubmed-article:8565117pubmed:ownerNLMlld:pubmed
pubmed-article:8565117pubmed:authorsCompleteYlld:pubmed
pubmed-article:8565117pubmed:pagination103-8lld:pubmed
pubmed-article:8565117pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:8565117pubmed:meshHeadingpubmed-meshheading:8565117-...lld:pubmed
pubmed-article:8565117pubmed:meshHeadingpubmed-meshheading:8565117-...lld:pubmed
pubmed-article:8565117pubmed:meshHeadingpubmed-meshheading:8565117-...lld:pubmed
pubmed-article:8565117pubmed:meshHeadingpubmed-meshheading:8565117-...lld:pubmed
pubmed-article:8565117pubmed:meshHeadingpubmed-meshheading:8565117-...lld:pubmed
pubmed-article:8565117pubmed:meshHeadingpubmed-meshheading:8565117-...lld:pubmed
pubmed-article:8565117pubmed:meshHeadingpubmed-meshheading:8565117-...lld:pubmed
pubmed-article:8565117pubmed:meshHeadingpubmed-meshheading:8565117-...lld:pubmed
pubmed-article:8565117pubmed:meshHeadingpubmed-meshheading:8565117-...lld:pubmed
pubmed-article:8565117pubmed:year1996lld:pubmed
pubmed-article:8565117pubmed:articleTitleInduction of 8-hydroxydeoxyguanosine in DNA by chromium(III) plus hydrogen peroxide and its prevention by scavengers.lld:pubmed
pubmed-article:8565117pubmed:affiliationDepartment of Life Sciences, National Tsing Hua University, Taipei, Taiwan, Republic of China.lld:pubmed
pubmed-article:8565117pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8565117pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:8565117lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:8565117lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:8565117lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:8565117lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:8565117lld:pubmed