Investigation of Glutathione S-Transferase Isoenzyme Protein Expression in Patients With Pterygium

dc.authorid0000-0002-7280-4417
dc.contributor.authorKaradağ, Remzi
dc.contributor.authorBayram, Nurettin
dc.contributor.authorOguztuzun, Serpil
dc.contributor.authorBozer, Busra
dc.contributor.authorBayramlar, Hüseyin
dc.contributor.authorSimsek, Gulcin Guler
dc.contributor.authorRapuano, Christopher J.
dc.date.accessioned2025-05-10T19:38:56Z
dc.date.issued2016
dc.departmentİstanbul Medeniyet Üniversitesi
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.
dc.identifier.doi10.1097/ICO.0000000000000827
dc.identifier.endpage1092
dc.identifier.issn0277-3740
dc.identifier.issn1536-4798
dc.identifier.issue8
dc.identifier.pmid27032026
dc.identifier.scopus2-s2.0-84962053253
dc.identifier.scopusqualityQ1
dc.identifier.startpage1089
dc.identifier.urihttps://doi.org/10.1097/ICO.0000000000000827
dc.identifier.urihttps://hdl.handle.net/20.500.14730/9500
dc.identifier.volume35
dc.identifier.wosWOS:000379669000016
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherLippincott Williams & Wilkins
dc.relation.ispartofCornea
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectetiopathogenesis
dc.subjectglutathione S-transferase
dc.subjectimmunohistochemical
dc.subjectoxidative stress
dc.subjectpterygium
dc.titleInvestigation of Glutathione S-Transferase Isoenzyme Protein Expression in Patients With Pterygium
dc.typeArticle

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