In vivo intraocular biomarkers: Changes of aqueous humor cytokines and chemokines in patients affected by uveal melanoma. Issue 38 (18th September 2020)

• Record Type: Journal Article
• Authors: Midena, Edoardo; Parrozzani, Raffaele; Midena, Giulia; Trainiti, Sara; Marchione, Giulia; Cosmo, Eleonora; Londei, Davide; Frizziero, Luisa
• Other Names: Zhu. Yi section editor.
• Is Part Of: Medicine. Volume 99:Issue 38(2020)
• Publication Date: 2020-09-18
• Subjects: aqueous humor sample -- biomarker -- chemokines -- cytokines -- factors -- growth -- proteomic analysis -- uveal melanoma; Medicine -- Periodicals; Medicine -- Periodicals; Médecine -- Périodiques; Geneeskunde; Medicine; Periodicals; Periodicals; 610.5
• DOI: 10.1097/MD.0000000000022091
• Languages: English
• ISSNs: 0025-7974

Abstract

Abstract : Abstract: Inflammatory, angiogenic, and immune processes have been associated with uveal melanoma (UM). The aim of the present study was to evaluate the presence of some specific aqueous humor (AH) soluble biomarkers in eyes affected by UM. Thirty-five eyes affected by primary UM and 35 control eyes, scheduled for cataract surgery, underwent full ophthalmic examination and AH sampling at time of surgery (brachytherapy or cataract surgery, respectively). AH samples were analyzed by means of ELISA, to detect the concentration of selected cytokines, chemokines, and growth factors. Compared with the control group, higher levels of IL-6 ( P = .049), IL-8 ( P = .006), RANTES ( P = .008), EGF ( P = .032), bFGF ( P = .016), MIF ( P = .007), and MCP ( P = .020) were detected in eyes with UM. VEGF concentration between the two groups was statistically borderline ( P = .058). Comparison between clinical characteristics and cytokine concentrations showed a positive correlation between tumor thickness and IL-8 ( P = .032), and degree of serous retinal detachment and IL-6 ( P = .021). UM is characterized by the presence of retinal neuroinflammatory, angiogenic, and immune biomarkers in AH. The proteomic analysis of AH could characterize UM microenvironment, allowing to better understand its pathophysiology.