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Updated: Feb 13, 2026

Whole Mount Immunofluorescent Staining of the Neonatal Mouse Retina to Investigate Angiogenesis In vivo
Published on: July 9, 2013
Gefitinib inhibits retina angiogenesis by affecting VEGF signaling pathway
Haitao Hu1, Lanxiang Hao2, Biao Yan3
1The Fourth School of Clinical Medicine, Nanjing Medical University, Nanjing, 210029, China; Eye Hospital of Nanjing Medical University, 138# Han-Zhong Road, Nanjing 210029, China; Yancheng City No. 1 People's Hospital, Yancheng, 224001, China.
Abstract:
Gefitinib, a small-molecule multitargeted tyrosine kinase inhibitor, is reported to be as a new oral antiangiogenic molecule. However, it is unknown whether Gefitinib inhibits retina angiogenesis. In this study, we aimed to investigate the effect of Gefitinib on oxygen-induced retinal angiogenesis and the correlation between Gefitinib and VEGF signaling pathway. 12 cases of mice models of oxygen-induced retinopathy were obtained by exposing to 75% oxygen for 7 days. Then, these models were randomly assigned to two groups, and treated with Gefitinib and DMSO, respectively. Retinal vascular morphology was evaluated by Ink staining, HE staining and isolectin staining. Finally, the expression levels of VEGF, Cyclin E, CDK2, CD31 were detected in retinal tissues. Results shown that newborn retinal vessels and oxygen-induced vaso-obliteration were easily to be observed in oxygen-induced groups compared with controls. Meanwhile, the number of nonganglion cells and neovascular nuclei in oxygen-induced groups was significantly increased compared with those in control groups. However, when treated with Gefitinib, newborn retinal vessels in mice models of oxygen-induced retinopathy were significantly reduced. Further investigation confirmed that Gefitinib treatment affected the VEGF/Cyclin E/CDK2/CD31 pathway. In conclusion, these findings indicate that Gefitinib is critical for the treatment of retina angiogenesis, which is associated with VEGF/Cyclin E/CDK2/CD31 pathway.
Insights
Gefitinib significantly reduces retinal angiogenesis in a mouse model by inhibiting the VEGF signaling pathway. This finding suggests Gefitinib
Area of Science:
- Ophthalmology
- Molecular Biology
- Pharmacology
Background:
- Retinal angiogenesis contributes to vision-threatening diseases.
- Gefitinib is an oral antiangiogenic agent, but its effect on retinal angiogenesis is unknown.
Purpose of the Study:
- To investigate Gefitinib's effect on oxygen-induced retinal angiogenesis.
- To explore the correlation between Gefitinib and the VEGF signaling pathway.
Main Methods:
- Oxygen-induced retinopathy mouse models were established.
- Mice were treated with Gefitinib or DMSO.
- Retinal vascular morphology was assessed using Ink, HE, and isolectin staining.
- VEGF, Cyclin E, CDK2, and CD31 expression levels were measured.
Main Results:
- Oxygen exposure increased retinal neovascularization and vaso-obliteration.
- Gefitinib treatment significantly reduced newborn retinal vessels.
- Gefitinib affected the VEGF/Cyclin E/CDK2/CD31 signaling pathway.
Conclusions:
- Gefitinib effectively inhibits retinal angiogenesis in a mouse model.
- The antiangiogenic effect of Gefitinib is linked to the VEGF/Cyclin E/CDK2/CD31 pathway.
- Gefitinib shows potential for treating retina angiogenesis.
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