Evidence map›Paper›PMID 42486827›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2026

[MBD1 knockdown inhibits proliferation, migration and angiogenesis of human umbilical vein endothelial cells

Yutong Dan, Tingfu Zhang, Hongmei Liu, Peng Zhang

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Yutong DanCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550004 , China.
Tingfu ZhangCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550004 , China.
Hongmei LiuCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550004 , China.
Peng ZhangCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550004 , China.

Funding

National Natural Science Foundation of China 32000601
6 · The paper itself

Abstract

objectivesTo investigate the effects of methyl-CpG binding domain protein 1 (MBD1) on proliferation, migration, and angiogenesis in human umbilical vein endothelial cells (HUVECs).

methodsCultured HUVECs were infected with a lentivirus carrying sh-MBD1 or a scramble shRNA (sh-NC), and the successfully infected cells were screened using puromycin. RT-qPCR and Western blotting were used to assess MBD1 gene silencing efficiency. The changes in proliferation, cell cycle, and migration of the infected cells were assessed using CCK-8 and colony formation assays, flow cytometry, scratch assay, and Transwell assay. The impact of MBD1 knockdown on angiogenic capacity of HUVECs was evaluated using angiogenesis assay. Immunofluorescence staining was used to investigate the expression of vascular endothelial growth factor A (VEGFA) in the infected HUVECs.

resultsCompared with the sh-NC cells, HUVECs infected with the lentivirus carrying sh-MBD1 exhibited significantly reduced proliferation capacity and migration ability. The total length of vessels formed

conclusionsMBD1 promotes proliferation, migration, and angiogenesis of HUVECs possibly by regulating the expression of VEGFA.

Indexed as

AngiogenesisCell MovementCell ProliferationDNA-Binding ProteinsHuman Umbilical Vein Endothelial CellsNeovascularization, PhysiologicTranscription FactorsCells, CulturedGene Knockdown TechniquesHumansLentivirusRNA, Small InterferingVascular Endothelial Growth Factor ADNA-Binding ProteinsMBD1 protein, humanRNA, Small InterferingTranscription FactorsVascular Endothelial Growth Factor AVEGFA protein, humanangiogenesiscell migrationcell proliferationhuman umbilical vein endothelial cellsmethyl-CpG-binding domain protein 1vascular endothelial growth factor A

Identifiers

PMID42486827
PMCPMC13391528

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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.