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Mediators of Inflammation
Volume 2013, Article ID 857380, 8 pages
http://dx.doi.org/10.1155/2013/857380
Research Article

Expression of VEGF-A, Otx Homeobox and p53 Family Genes in Proliferative Vitreoretinopathy

1Department of Surgical and Morphological Sciences, Section of Ophthalmology, University of Insubria, Ospedale di Circolo, Via F. Guicciardini 9, 21100 Varese, Italy
2Department of Clinical and Experimental Medicine, University of Insubria, Via O. Rossi 9, 21100 Varese, Italy
3Ph.D. Program in Biotechnology, School of Biological and Medical Sciences, University of Insubria, Via O. Rossi 9, 21100 Varese, Italy
4Pathology Institute, Ospedale di Circolo, Via F. Guicciardini 9, 21100 Varese, Italy
5Eye Clinic, Second University of Napoli, Via S. Pansini 5, 80131 Napoli, Italy

Received 19 July 2013; Accepted 2 September 2013

Academic Editor: Mario R. Romano

Copyright © 2013 Claudio Azzolini et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Introduction. Proliferative vitreoretinopathy (PVR) is a severe inflammatory complication of retinal detachment. Pathological epiretinal membranes grow on the retina surface leading to contraction, and surgery fails in 5% to 10% of the cases. We evaluated the expression of VEGF-A, Otx1, Otx2, Otx3, and p53 family members from PVR specimens to correlate their role in inducing or preventing the pathology. Methods. Twelve retinal samples were taken from patients affected by PVR during therapeutic retinectomies in vitreoretinal surgery. Gene expression was evaluated using quantitative real-time reverse transcriptase PCR analysis and immunohistochemistry, using four healthy human retinae as control. Result. Controls showed basal expression of all genes. PVR samples showed little or no expression of Otx1 and variable expression of VEGF-A, Otx2, Otx3, p53, and p63 genes. Significant correlation was found among VEGF-A, Otx2, p53, and p63 and between Otx1 and Otx3. Conclusions. Otx homeobox, p53 family, and VEGF-A genes are expressed in PVR human retina. We individuated two possible pathways (VEGF-A, Otx2, p53, p63 and Otx1 and Otx3) involved in PVR progression that could influence in different manners the course of the pathology. Individuating the genetic pathways of PVR represents a novel approach to PVR therapies.