Abstract | BACKGROUND: 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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Authors | Min Zhao, Wan-Kun Xie, Yu-Jing Bai, Lyu-Zhen Huang, Bin Wang, Jian-Hong Liang, Hong Yin, Xiao-Xin Li, Xuan Shi |
Journal | Chinese medical journal
(Chin Med J (Engl))
Vol. 128
Issue 18
Pg. 2505-9
(Sep 20 2015)
ISSN: 2542-5641 [Electronic] China |
PMID | 26365970
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Protein Isoforms
- VEGFA protein, human
- Vascular Endothelial Growth Factor A
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Topics |
- Enzyme-Linked Immunosorbent Assay
- Female
- Humans
- Infant, Newborn
- Infant, Premature
- Male
- Prospective Studies
- Protein Isoforms
(metabolism)
- Retinopathy of Prematurity
(metabolism)
- Vascular Endothelial Growth Factor A
(metabolism)
- Vitreous Body
(metabolism)
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