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dc.creatorĐelić, Ninoslav
dc.creatorĐelić, D
dc.date.accessioned2020-06-03T12:46:37Z
dc.date.available2020-06-03T12:46:37Z
dc.date.issued2002
dc.identifier.issn0188-4409
dc.identifier.urihttps://vet-erinar.vet.bg.ac.rs/handle/123456789/217
dc.description.abstractBackground. Epidemiologic data and animal experiments strongly implicate that steroid hormones are involved in the process of malignant transformation due to their capability to stimulate mitotic division and/or elevate the level of Mutations in susceptible cells. Methods. The objectives of this investigation were to evaluate the effects of 17beta estradiol in sister-chromatid exchange (SCE) test on cultured human peripheral blood lymphocytes. The lowest concentration of 17beta estradiol used in this experiment (10(-10) M) was calculated as comparable with the physiologic blood level of 17beta estradiol in women. Three experimental concentrations corresponded to minimal (7 X 10(-8) M), average (3.5 X 10(-6) M), and maximal (7 X 10(-6) M) therapeutic doses in human medicine. In addition, the highest concentrations exceed maximal therapeutic dose 10-fold (7 X 10(-5) M) and 30-fold (2.1 X 10 (4) M), respectively. Results. The obtained results indicate that estradiol significantly elevates SCE per cell frequency tit all concentrations applied except at the lowest one. However. estradiol has not influenced mitotic activity of cultured human lymphocytes significantly. Conclusions. It can be concluded that 17beta estradiol expressed genotoxic effects and therefore fright represent a human health risk.en
dc.publisherElsevier Science Inc, New York
dc.rightsrestrictedAccess
dc.sourceArchives of Medical Research
dc.subjectestradiolen
dc.subjectgenotoxicityen
dc.subjectsister-chromatid exchangeen
dc.subjectcanceren
dc.subjectlymphocyteen
dc.titleEnhanced sister-chromatid exchange rate in human lymphocytes exposed to 17 beta estradiol in vitroen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractЂелић, Нинослав; Ђелић, Д;
dc.citation.volume33
dc.citation.issue2
dc.citation.spage148
dc.citation.epage151
dc.citation.other33(2): 148-151
dc.citation.rankM23
dc.identifier.wos000174435800009
dc.identifier.doi10.1016/S0188-4409(01)00355-1
dc.identifier.pmid11886713
dc.identifier.scopus2-s2.0-0036124757
dc.type.versionpublishedVersion


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