Evidence map›Paper›PMID 33274003›Full record

ArticleOxidative medicine and cellular longevity2020

Sodium Butyrate Inhibits Neovascularization Partially via TNXIP/VEGFR2 Pathway.

Xiaoqiang Xiao, Min Chen, Yanxuan Xu, Shaofen Huang, Jiajian Liang, Yingjie Cao, Haoyu Chen

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Short-Chain Fatty Acids and the Gut-Retina Connection: A Systematic Review.International journal of molecular sciences · 2025
    Pooled it
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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

7 authors at 1 institution in 2 countries.

Xiaoqiang XiaoJoint Shantou International Eye Center, Shantou University and the Chinese University of Hong Kong, Shantou, China.ORCID https://orcid.org/0000-0001-8274-4780
Min ChenJoint Shantou International Eye Center, Shantou University and the Chinese University of Hong Kong, Shantou, China.
Yanxuan XuJoint Shantou International Eye Center, Shantou University and the Chinese University of Hong Kong, Shantou, China.
Shaofen HuangJoint Shantou International Eye Center, Shantou University and the Chinese University of Hong Kong, Shantou, China.
Jiajian LiangJoint Shantou International Eye Center, Shantou University and the Chinese University of Hong Kong, Shantou, China.
Yingjie CaoJoint Shantou International Eye Center, Shantou University and the Chinese University of Hong Kong, Shantou, China.
Haoyu ChenJoint Shantou International Eye Center, Shantou University and the Chinese University of Hong Kong, Shantou, China.ORCID https://orcid.org/0000-0003-0676-4610
Chinese University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Control of neovascularization with small molecules is a promising tactics. Here, we tested the roles of sodium butyrate (NaBu) on the neovascularization and primary explained its underlining molecular links. We used models including cell and ex vivo culture of choroid and mouse, as well as the biochemical and cellular techniques, to confirm our hypothesis. We found that treating HUVEC cells with NaBu (both 2.5 mM and 5 mM) significantly inhibited its ability in tube formation and proliferation. This inhibitory effect was also observed in choroid sprouting experiments, compared to the control. Interestingly, the choroid sprouting suppressed by NaBu can proliferate again after removing it, indicating that the cell cycle progression might be arrested. The laser-induced choroid neovascularization (CNV) was significantly alleviated by assessing the CNV size (decreased to 0.73 fold) in contrast with the vehicle control group after 2.5 mM NaBu injection for 7 days. Mechanistically, we found an enhanced TXNIP expression in response to NaBu treatment in all the three models. Overexpressing TXNIP in HUVEC cells blocked its tube formation and inhibited its proliferation; on the other hand, knocking down its expression with shRNA reversed those phenotypes in context of NaBu treatment. Further investigation showed the expression of VEGF receptor 2 (VEGFR2) in HUVEC cells was regulated by TXNIP undergoing NaBu treatment. We therefore argued that NaBu inhibited neovascularization partially through TXNIP-regulated VEGFR2 signal pathway.

Indexed as

Choroidal NeovascularizationAnimalsButyric AcidCarrier ProteinsHumansHuman Umbilical Vein Endothelial CellsMiceSignal TransductionThioredoxinsVascular Endothelial Growth Factor Receptor-2Butyric AcidCarrier ProteinsKDR protein, humanKdr protein, mouseThioredoxinsTXNIP protein, humanTxnip protein, mouseVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID33274003
PMCPMC7700023
OpenAlexW3107208349

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.