2019
DOI: 10.5935/0004-2749.20190103
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Mechanisms and biomarker candidates in pterygium development

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Cited by 38 publications
(36 citation statements)
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“…Pterygium is characterized by in ammatory in ltrates, brosis, proliferation, angiogenesis and extracellular matrix breakdown and its pathogenesis is mainly associated with long-term exposure to ultraviolet radiation [1]. Moreover, apoptotic and oncogenic proteins, DNA methylation, lymphangiogenesis, viral infection, extracellular matrix modulators, in ammatory mediators, loss of heterozygosity, microsatellite instability, alterations in cholesterol metabolism and epithelialmesenchymal cell transition have been identi ed as other causes [2].…”
Section: Discussionmentioning
confidence: 99%
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“…Pterygium is characterized by in ammatory in ltrates, brosis, proliferation, angiogenesis and extracellular matrix breakdown and its pathogenesis is mainly associated with long-term exposure to ultraviolet radiation [1]. Moreover, apoptotic and oncogenic proteins, DNA methylation, lymphangiogenesis, viral infection, extracellular matrix modulators, in ammatory mediators, loss of heterozygosity, microsatellite instability, alterations in cholesterol metabolism and epithelialmesenchymal cell transition have been identi ed as other causes [2].…”
Section: Discussionmentioning
confidence: 99%
“…UV irradiation relays its toxic impacts either directly by UV phototoxicity or indirectly by formation of primary molecules causing oxidative damage (aka reactive oxygen species or ROS). Imbalance between growth factors and cytokines, changes in tear lm, viral infections, genetic mutations, immunologic disturbances and chronic in ammation are also believed to be the important factors [2].…”
Section: Introductionmentioning
confidence: 99%
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“…Excessive exposure to UVB (especially by way of OS) is one of the most important causes of pterygium [35]. UVB radiation may cause toxic light damage to DNA directly or by increasing ROS, which causes DNA damage [53]. In patients with pterygium, the serum total oxidant status (TOS), total antioxidant status (TAS), and nitric oxide (NO) and MDA content were significantly increased, and the antioxidant enzyme (SOD, CAT, and GPX) content was decreased [54,55], indicating an increase in nonenzyme antioxidant activity.…”
Section: Fuchs' Endothelial Corneal Dystrophy (Fecd)mentioning
confidence: 99%
“…Verschiedene Studien haben bereits mögliche molekulare Mechanismen der Pterygiumentstehung untersucht [1][2][3][4][5][6]. Diese molekularen Mechanismen umfassen, teilweise durch UV-Strahlung oder virale Infektionen initiiert, unter anderem oxidativen Stress, Modulation der Extrazellularmatrix, Veränderung der Expression von apoptotischen Proteinen und Tumorsuppressorgenen, Verlust der Heterozygose, DNA-Methylierung, erhöhte Expression von Entzündungsmediatoren, gesteigerte (Lymph-)Angiogenese und Veränderungen des Cholesterinstoffwechsels [1][2][3][4][5].…”
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