Uzuncakmak Tugba Kevser, Koska Mahmut Can, Ozkanli Seyma, Kaya Kocdogan Arzu, Oguztuzun Serpil, Karadag Ayse Serap, Akdeniz Necmettin, Wollina Uwe
Department of Dermatology, Istanbul Medeniyet University, School of Medicine, Goztepe Training and Research Hospital, Istanbul, Turkey.
Department of Pathology, Istanbul Medeniyet University, School of Medicine, Goztepe Training and Research Hospital, Istanbul, Turkey.
Dermatol Ther. 2020 Nov;33(6):e14363. doi: 10.1111/dth.14363. Epub 2020 Oct 8.
Morphea is an inflammatory connective tissue disorder, which is characterized by sclerosis in skin and subcutaneous tissues with a chronic progress. The oxidative stress in pathogenesis of sclerosing diseases was proposed in several studies with conflicting results. To explore the tissue expressions of Glutathione S transferase (GST) isoenzymes in patients with morphea and compare these expressions with healthy controls. Twenty-two morphea patients and 20 sex and age matched healthy controls were enrolled in this study. Four millimeter punch biopsies were performed from the active sclerotic plaques of morphea patients. Tissue samples of control group were obtained from nonlesional normal skin biopsy specimens. The protein expressions of GST isoenzymes were analyzed immunohistochemically. Tissue expressions of GSTP1, GSTT1, and GSTA1 isoenzymes in morphea patients were found to be significantly higher than in control tissues. There was no significant difference in GSTM1 isoenzyme expression between the two groups. The increased tissue expressions of GSTA1, GSTP1, and GSTT1 isoenzymes in morphea may represent the activated GST enzymes in response to excessive free radical formation and may also support the hypothesis of increased oxidative stress in morphea etiopathogenesis.
硬斑病是一种炎症性结缔组织疾病,其特征是皮肤和皮下组织硬化且病程呈慢性。多项研究提出了硬化性疾病发病机制中的氧化应激,但结果相互矛盾。为了探究硬斑病患者谷胱甘肽S转移酶(GST)同工酶的组织表达情况,并将这些表达与健康对照进行比较。本研究纳入了22例硬斑病患者和20例年龄及性别匹配的健康对照。从硬斑病患者的活动性硬化斑块处取4毫米的打孔活检组织。对照组的组织样本取自非病变正常皮肤活检标本。采用免疫组织化学方法分析GST同工酶的蛋白表达。发现硬斑病患者中GSTP1、GSTT1和GSTA1同工酶的组织表达显著高于对照组织。两组之间GSTM1同工酶表达无显著差异。硬斑病中GSTA1、GSTP1和GSTT1同工酶组织表达的增加可能代表GST酶因自由基过度形成而被激活,也可能支持硬斑病病因发病机制中氧化应激增加的假说。