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dc.contributor.authorSezgin, Burak
dc.contributor.authorKinci, Mehmet F.
dc.contributor.authorPirinççi, Fatih
dc.contributor.authorCamuzcuoğlu, Aysun
dc.contributor.authorErel, Özcan
dc.contributor.authorNeşelioğlu, Salim
dc.contributor.authorCamuzcuoğlu, Hakan
dc.date.accessioned2020-11-20T14:30:03Z
dc.date.available2020-11-20T14:30:03Z
dc.date.issued2020
dc.identifier.issn1341-8076
dc.identifier.issn1447-0756
dc.identifier.urihttps://doi.org/10.1111/jog.14480
dc.identifier.urihttps://hdl.handle.net/20.500.12809/329
dc.descriptionWOS: 000567507700001en_US
dc.descriptionPubMed ID: 32909381en_US
dc.description.abstractAim The evaluation of dynamic thiol-disulfide homeostasis among patients with the cancer of the uterine cervix. Methods The study was conducted in 62 cervical cancer patients and 61 healthy women who had been followed up in an obstetrics and gynecology clinic between September 2018 and April 2020. Serum disulfide, native thiol, total thiol, ischemia modified-albumin, total antioxidant and oxidant capacities, and oxidative stress index values were measured in all participants. Results The mean plasma disulfide levels of the cervical cancer group was statistically significantly higher than that of the control group (25.79 +/- 6.90 mu mol/L, 22.31 +/- 6.11 mu mol/L, respectively) (P= 0.004). Plasma native thiol and total thiol levels were lower in cervical cancer patients (299.27 +/- 99.05 mu mol/L and 350.86 +/- 102.72 mu mol/L, respectively) compared to controls, but no statistically significant difference was observed (318.00 +/- 93.75 mu mol/L and 376.44 +/- 98.51 mu mol/L, respectively) (P= 0.284,P= 0.161). With respect to the ischemia modified-albumin level, no statistically significant difference was observed between two groups. There were statistically significant positive association between disulfide level and both the stage of cervical cancer (r= 0.278,P= 0.029) and total oxidant capacity level (r= 0.256,P= 0.046). Conclusion Dynamic thiol-disulfide homeostasis may participate in the pathophysiological mechanisms of cervical cancer and may be a potential biomarker for early identification of cervical cancer in future.en_US
dc.item-language.isoengen_US
dc.publisherWileyen_US
dc.item-rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCervical Canceren_US
dc.subjectDisulfideen_US
dc.subjectIschemia Modified Albuminen_US
dc.subjectOxidant-Antioxidant Exchangeen_US
dc.subjectThiolen_US
dc.titleThiol-disulfidestatus of patients with cervical canceren_US
dc.item-typearticleen_US
dc.contributor.departmentMÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.contributor.departmentMÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü
dc.contributor.institutionauthorSezgin, Burak
dc.contributor.institutionauthorKinci, Mehmet F.
dc.contributor.institutionauthorPirinççi, Fatih
dc.identifier.doi10.1111/jog.14480
dc.identifier.volume46
dc.identifier.issue11
dc.relation.journalJournal of Obstetrics and Gynaecology Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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