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Expression of Total Vascular Endothelial Growth Factor and the Anti-angiogenic VEGF(165)b Isoform in the Vitreous of Patients with Retinopathy of Prematurity

BACKGROUND: This study was to examine the expression of total vascular endothelial growth factor (VEGF) and the anti-angiogenic VEGF(165)b isoform in the vitreous body of retinopathy of prematurity (ROP) patients, and to further study the role of the VEGF splicing in the development of ROP. METHODS:...

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Autores principales: Zhao, Min, Xie, Wan-Kun, Bai, Yu-Jing, Huang, Lyu-Zhen, Wang, Bin, Liang, Jian-Hong, Yin, Hong, Li, Xiao-Xin, Shi, Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725572/
https://www.ncbi.nlm.nih.gov/pubmed/26365970
http://dx.doi.org/10.4103/0366-6999.164937
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author Zhao, Min
Xie, Wan-Kun
Bai, Yu-Jing
Huang, Lyu-Zhen
Wang, Bin
Liang, Jian-Hong
Yin, Hong
Li, Xiao-Xin
Shi, Xuan
author_facet Zhao, Min
Xie, Wan-Kun
Bai, Yu-Jing
Huang, Lyu-Zhen
Wang, Bin
Liang, Jian-Hong
Yin, Hong
Li, Xiao-Xin
Shi, Xuan
author_sort Zhao, Min
collection PubMed
description BACKGROUND: This study was to examine the expression of total vascular endothelial growth factor (VEGF) and the anti-angiogenic VEGF(165)b isoform in the vitreous body of retinopathy of prematurity (ROP) patients, and to further study the role of the VEGF splicing in the development of ROP. METHODS: This was a prospective clinical laboratory investigation study. All patients enrolled received standard ophthalmic examination with stage 4 ROP that required vitrectomy to collect the vitreous samples. The control samples were from congenital cataract patients. The expression of total VEGF and the anti-angiogenic VEGF(165)b were measured by enzyme-linked immunosorbent assay. Results were analyzed statistically using nonparametric tests. RESULTS: The total VEGF level was markedly elevated in ROP samples while VEGF(165)b was markedly decreased compared to control group. The relative protein expression level of VEGF(165)b isoform was significantly decreased in ROP patients which were correlated with the ischemia-induced neovascularization. CONCLUSIONS: There was a switch of VEGF splicing from anti-angiogenic to pro-angiogenic family in ROP patients. A specific inhibitor that more selectively targets VEGF(165)and controls the VEGF splicing between pro- and anti-angiogenic families might be a more effective therapy for ROP.
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spelling pubmed-47255722016-04-04 Expression of Total Vascular Endothelial Growth Factor and the Anti-angiogenic VEGF(165)b Isoform in the Vitreous of Patients with Retinopathy of Prematurity Zhao, Min Xie, Wan-Kun Bai, Yu-Jing Huang, Lyu-Zhen Wang, Bin Liang, Jian-Hong Yin, Hong Li, Xiao-Xin Shi, Xuan Chin Med J (Engl) Original Article BACKGROUND: This study was to examine the expression of total vascular endothelial growth factor (VEGF) and the anti-angiogenic VEGF(165)b isoform in the vitreous body of retinopathy of prematurity (ROP) patients, and to further study the role of the VEGF splicing in the development of ROP. METHODS: This was a prospective clinical laboratory investigation study. All patients enrolled received standard ophthalmic examination with stage 4 ROP that required vitrectomy to collect the vitreous samples. The control samples were from congenital cataract patients. The expression of total VEGF and the anti-angiogenic VEGF(165)b were measured by enzyme-linked immunosorbent assay. Results were analyzed statistically using nonparametric tests. RESULTS: The total VEGF level was markedly elevated in ROP samples while VEGF(165)b was markedly decreased compared to control group. The relative protein expression level of VEGF(165)b isoform was significantly decreased in ROP patients which were correlated with the ischemia-induced neovascularization. CONCLUSIONS: There was a switch of VEGF splicing from anti-angiogenic to pro-angiogenic family in ROP patients. A specific inhibitor that more selectively targets VEGF(165)and controls the VEGF splicing between pro- and anti-angiogenic families might be a more effective therapy for ROP. Medknow Publications & Media Pvt Ltd 2015-09-20 /pmc/articles/PMC4725572/ /pubmed/26365970 http://dx.doi.org/10.4103/0366-6999.164937 Text en Copyright: © 2015 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Zhao, Min
Xie, Wan-Kun
Bai, Yu-Jing
Huang, Lyu-Zhen
Wang, Bin
Liang, Jian-Hong
Yin, Hong
Li, Xiao-Xin
Shi, Xuan
Expression of Total Vascular Endothelial Growth Factor and the Anti-angiogenic VEGF(165)b Isoform in the Vitreous of Patients with Retinopathy of Prematurity
title Expression of Total Vascular Endothelial Growth Factor and the Anti-angiogenic VEGF(165)b Isoform in the Vitreous of Patients with Retinopathy of Prematurity
title_full Expression of Total Vascular Endothelial Growth Factor and the Anti-angiogenic VEGF(165)b Isoform in the Vitreous of Patients with Retinopathy of Prematurity
title_fullStr Expression of Total Vascular Endothelial Growth Factor and the Anti-angiogenic VEGF(165)b Isoform in the Vitreous of Patients with Retinopathy of Prematurity
title_full_unstemmed Expression of Total Vascular Endothelial Growth Factor and the Anti-angiogenic VEGF(165)b Isoform in the Vitreous of Patients with Retinopathy of Prematurity
title_short Expression of Total Vascular Endothelial Growth Factor and the Anti-angiogenic VEGF(165)b Isoform in the Vitreous of Patients with Retinopathy of Prematurity
title_sort expression of total vascular endothelial growth factor and the anti-angiogenic vegf(165)b isoform in the vitreous of patients with retinopathy of prematurity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725572/
https://www.ncbi.nlm.nih.gov/pubmed/26365970
http://dx.doi.org/10.4103/0366-6999.164937
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