Expression of Gstm4 and Gstt1 in Patients With Tinea Versicolor, Tinea Inguinalis and Tinea Pedis Infections: a Preliminary Study

dc.contributor.author Kilic, M.
dc.contributor.author Oguztuzun, S.
dc.contributor.author Karadag, A. S.
dc.contributor.author Cakir, E.
dc.contributor.author Aydin, M.
dc.contributor.author Ozturk, L.
dc.date.accessioned 2025-05-10T17:26:04Z
dc.date.available 2025-05-10T17:26:04Z
dc.date.issued 2011
dc.description Kilic, Murat/0000-0002-1377-2021 en_US
dc.description.abstract Background. Several skin diseases are believed to be associated with oxidative stress. Defence against reactive oxygen species in the skin involves a variety of antioxidant enzymes, including glutathione-S-transferases (GSTs) catalysing the reaction between reduced glutathione, and a variety of exogenously and endogenously derived electrophilic compounds. The mammalian soluble GSTs are divided into five main classes: alpha (A), mu (M), pi (P), theta (T) and zeta (Z). Aim. To investigate the expression of GSTM4 and GSTT1 in lesional and nonlesional skin of patients with dermatophytoses and Tinea versicolor infection. Methods. Expression of GSTM4 and GSTT1 was assessed by immunohistochemistry for dermatophytoses in 15 patients with T. versicolor, 15 patients with Tinea pedis and 8 patients with Tinea inguinalis, and compared with healthy controls (n = 9). After written consent was signed by each participant, punch biopsies were excised from the centre of the lesional skin sites in patients and from the normal skin sites in controls. The relationships between expression of GSTM4 and GSTT1 isoenzymes and fungal infections were also examined. Results. When the normal and infected tissue of these cases were compared according to their staining intensity, GSTM4 expression was found to be stronger in control epithelium than in the epithelium of patients with T. pedis, T. inguinalis or T. versicolor (P < 0.05). By contrast, expression of GSTT1 was stronger in the epithelium of patients infected with any of the three dermatophytes than in control epithelium (P < 0.05). Conclusions. There is a significant relationship between presence of T. versicolor, T. inguinalis and T. pedis and expression of GSTM4 and GSTT1. en_US
dc.identifier.doi 10.1111/j.1365-2230.2010.03991.x
dc.identifier.issn 0307-6938
dc.identifier.issn 1365-2230
dc.identifier.scopus 2-s2.0-79960573475
dc.identifier.uri https://doi.org/10.1111/j.1365-2230.2010.03991.x
dc.identifier.uri https://hdl.handle.net/20.500.14720/11565
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.title Expression of Gstm4 and Gstt1 in Patients With Tinea Versicolor, Tinea Inguinalis and Tinea Pedis Infections: a Preliminary Study en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Kilic, Murat/0000-0002-1377-2021
gdc.author.scopusid 57214488014
gdc.author.scopusid 26644418800
gdc.author.scopusid 26425048800
gdc.author.scopusid 16401003200
gdc.author.scopusid 56675387200
gdc.author.scopusid 36712272200
gdc.author.wosid Karadag, Ayse/V-7974-2018
gdc.author.wosid Kilic, Murat/V-4843-2017
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Kilic, M.; Oguztuzun, S.] Kirikkale Univ, Dept Biol, TR-71450 Yahsihan, Kirikkale, Turkey; [Karadag, A. S.] Yuzuncu Yil Univ, Fac Med, Dept Dermatol, Van, Turkey; [Cakir, E.] Inonu Univ, Fac Med, Dept Pathol, Malatya, Turkey; [Aydin, M.] Van Educ & Res Hosp, Dept Pathol, Van, Turkey; [Ozturk, L.] Kirikkale Univ, Dept Econ, Fac Econ & Adm Sci, TR-71450 Yahsihan, Kirikkale, Turkey en_US
gdc.description.endpage 594 en_US
gdc.description.issue 6 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 590 en_US
gdc.description.volume 36 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q1
gdc.identifier.pmid 21771003
gdc.identifier.wos WOS:000292920800004
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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