Evidence map›Paper›PMID 38250154›Full record

ArticleInternational journal of biological sciences2024

Angiogenic and Fibrogenic Dual-effect of Gremlin1 on Proliferative Diabetic Retinopathy.

Xinjing Wu, Bing Qin, Ruiwen Cheng, Ru Zhou, Xingxing Wang, Zhengyu Zhang, Xiying Mao, Zhan Xie, Mingkang Chen, Lin Jiang and 6 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
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

6 citing papers in PubMed, 6 citations in OpenAlex.

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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

16 authors at 2 institutions in 1 country.

Xinjing WuDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Bing QinDepartment of Ophthalmology, The Affiliated Suqian First People's Hospital of Nanjing Medical University, Suqian 223800, China.
Ruiwen ChengDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Ru ZhouDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Xingxing WangDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Zhengyu ZhangDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Xiying MaoDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Zhan XieDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Mingkang ChenDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Lin JiangDepartment of Endocrinology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Ping XieDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Jiangdong JiDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Weiwei ZhangDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Songtao YuanDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Zizhong HuDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Qinghuai LiuDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Nanjing Medical University · CNJiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ocular angiogenic diseases, such as proliferative diabetic retinopathy (PDR), are often characterized by pathological new vessels and fibrosis formation. Anti-vascular endothelial growth factor (VEGF) therapy, despite of its efficiency to inhibit new vessels, has limitations, including drug resistance and retinal fibrosis. Here, we identified that Gremlin1, a novel angiogenesis and fibrosis inducer, was secreted from Müller glial cells, and its expression increased in the vitreous fluid from patients with PDR. Mechanistically, Gremlin1 triggered angiogenesis by promoting endothelial-mesenchymal transition via the EGFR/RhoA/ROCK pathway. In addition, Gremlin1 activated microglia to present profibrotic and fibrogenic properties. Further, anti-Gremlin1 antibody inhibited ocular angiogenesis and microglia fibrosis in mouse models. Collectively, Gremlin1 could be a potential therapeutic target in the treatment of ocular angiogenic diseases.

Indexed as

Diabetes MellitusDiabetic RetinopathyIntercellular Signaling Peptides and ProteinsAnimalsBiological TransportDisease Models, AnimalEyeFibrosisHumansMiceGREM1 protein, humanIntercellular Signaling Peptides and ProteinsAngiogenesisFibrosisGremlin1MicrogliaProliferative diabetic retinopathy

Identifiers

PMID38250154
PMCPMC10797694
OpenAlexW4391036479

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.