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dc.contributor.authorKaradag, Remzi
dc.contributor.authorBayram, Nurettin
dc.contributor.authorOguztuzun, Serpil
dc.contributor.authorBozer, Busra
dc.contributor.authorBayramlar, Huseyin
dc.contributor.authorSimsek, Gulcin Guler
dc.contributor.authorRapuano, Christopher J.
dc.date.accessioned2020-06-25T18:16:24Z
dc.date.available2020-06-25T18:16:24Z
dc.date.issued2016
dc.identifier.citationclosedAccessen_US
dc.identifier.issn0277-3740
dc.identifier.issn1536-4798
dc.identifier.urihttps://doi.org/10.1097/ICO.0000000000000827
dc.identifier.urihttps://hdl.handle.net/20.500.12587/6519
dc.descriptionBozer, Busra/0000-0002-7280-4417en_US
dc.descriptionWOS: 000379669000016en_US
dc.descriptionPubMed: 27032026en_US
dc.description.abstractPurpose: We investigated glutathione S-transferase (GST) enzymes in terms of their potential effects on the pathogenesis of pterygium. Methods: Twenty-six pterygium specimens and 15 normal conjunctival specimens of 15 control subjects were investigated. Expressions of GST (alpha, mu, pi, and theta) enzymes were assessed by immunohistochemical staining. A brown color in the cytoplasm and/or nuclei of epithelial cells was evaluated as positive staining for GST enzymes. For each antibody, the intensity of the reaction [negative (-), weak (1+), moderate (2+), or strong (3+)] was determined to describe the immunoreactions. Results: The median age was 52 years in the both groups. There was no significant difference between the groups in terms of age, sex, and intraocular pressure measurements (P > 0.05 for all). Of the 26 pterygium specimens, 15 (57.7%) (8 weak, 4 moderate, and 3 strong staining) were identified with GST pi-1 (GSTP1) expression and 20 (76.9%) (12 weak, 7 moderate, and 1 strong staining) with GST theta-1 (GSTT1) expression. Of the 15 control specimens, 4 (26.7%) (4 weak staining) were identified with the GSTP1 expression, and 1 (6.7%) with GSTT1 expression. GSTP1 and GSTT1 expressions were significantly higher in the pterygium specimens than in the controls (P = 0.043, P < 0.001; respectively). None of tissue specimens had positive staining for GST mu-1 or GST alpha-1 in both groups (both; P = 1.00). Conclusions: The significant increase of GSTP1 and GSTT1 expressions in pterygium may be because of the increased activation of GST in response to excessive free radical formation from ultraviolet exposure to maintain antioxidant capacity in pterygium.en_US
dc.language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.isversionof10.1097/ICO.0000000000000827en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectetiopathogenesisen_US
dc.subjectglutathione S-transferaseen_US
dc.subjectimmunohistochemicalen_US
dc.subjectoxidative stressen_US
dc.subjectpterygiumen_US
dc.titleInvestigation of Glutathione S-Transferase Isoenzyme Protein Expression in Patients With Pterygiumen_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume35en_US
dc.identifier.issue8en_US
dc.identifier.startpage1089en_US
dc.identifier.endpage1092en_US
dc.relation.journalCorneaen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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