Evidence map›Paper›PMID 40764625›Full record

ArticleScientific reports2025

Comparative analysis of bevacizumab and sorafenib on the survival of retinal ganglion cells in the treatment of retinal diseases.

Wungrak Choi, Jin-Ok Choi, Min Kyung Chae, Min Seok Kim, Chan Yun Kim

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Wungrak ChoiDepartment of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun- gu, Seoul, 03722, Korea.
Jin-Ok ChoiDepartment of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun- gu, Seoul, 03722, Korea.
Min Kyung ChaeDepartment of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun- gu, Seoul, 03722, Korea.
Min Seok KimDepartment of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun- gu, Seoul, 03722, Korea.
Chan Yun KimDepartment of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun- gu, Seoul, 03722, Korea. KCYEYE@yuhs.ac.

Funding

National Research Foundation of Korea 2025-00562090National Research Foundation of Korea RS-2024-00405287Research Grant from Gangnam Severance Hospital D-2023-0012
6 · The paper itself

Abstract

This study investigates the effects of bevacizumab, a common vascular endothelial growth factor (VEGF) inhibitor, in treating ocular neovascular disorders, with a focus on its impact on retinal ganglion cell (RGC) survival. Given that bevacizumab has been associated with adverse effects on RGCs, we aimed to validate these reports, identify an alternative VEGF inhibitor with similar antiangiogenic efficacy but without detrimental effects on RGCs, and explore the underlying mechanisms. Using primary RGCs extracted from neonatal rats and human umbilical vascular endothelial cells (HUVECs), we compared the efficacy of bevacizumab with other VEGF inhibitors and assessed the apoptotic effects and cell survival pathways influenced by these treatments. Our results showed that while both sorafenib and bevacizumab exhibited potent VEGF-inhibitory effects in HUVECs, sorafenib led to significantly higher RGC survival rates compared to bevacizumab. Western blot analysis indicated that bevacizumab treatment resulted in lower Akt levels than sorafenib, and RNA sequencing revealed that the PI3K/AKT, Ras, and MAPK signaling pathways play crucial roles in RGC viability. These findings suggest that sorafenib may offer a safer and more effective alternative to bevacizumab for treating retinal diseases, with potential implications for the development of safer therapeutic approaches, particularly in conditions like glaucoma.

Indexed as

Angiogenesis InhibitorsBevacizumabRetinal DiseasesRetinal Ganglion CellsSorafenibAnimalsApoptosisCell SurvivalHumansHuman Umbilical Vein Endothelial CellsRatsRats, Sprague-DawleySignal TransductionVascular Endothelial Growth Factor AAngiogenesis InhibitorsBevacizumabSorafenibVascular Endothelial Growth Factor ABevacizumabGlaucomaRetinal ganglion cellSorafenibVascular endothelial growth factor

Identifiers

PMID40764625
PMCPMC12325771

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.