Evidence map›Paper›PMID 40537794›Full record

ArticleJournal of nanobiotechnology2025

MIL-53(Fe)-Glucose self-assembled complex for enhanced angiogenesis and endothelial tip cell activation.

Jie Wu, Leyi Liu, Runze Li, Kuangwu Pan, Duoling Xu, Chao Wang, Yuhao Liu, Chao Wang, Yi He, Weijie Zhuang and 3 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

13 authors.

Jie Wu *Hospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Leyi Liu *Hospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Runze Li *Hospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Kuangwu PanHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Duoling XuHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Chao WangHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Yuhao LiuHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Chao WangCenter for Infectious Disease Research, School of Medicine, Westlake University, Hangzhou, 310012, China.
Yi HeHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Weijie ZhuangHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Kechen LiHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China.
Wei ZhaoHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China. zhaowei3@mail.sysu.edu.cn.
Dongsheng YuHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, 510055, China. yudsh@mail.sysu.edu.cn.

Funding

National Natural Science Foundation of China 82373255Natural Science Foundation of Guangdong Province 2024A1515012918Special Funds for the Cultivation of Guangdong College Students' Scientific and Technological Innovation pdjh2024b018
6 · The paper itself

Abstract

Critical bone defects continue to pose a critical challenge in clinical settings. Facilitating rapid and thorough vascularization during bone regeneration is advantageous for the repair of substantial bone defects. Presently, the application of carriers to deliver pharmacological agents or growth factors to bone deficiency areas is an effective strategy for promoting vascularization within bone tissue, with the selection of appropriate carriers being of paramount importance. Because of its unique breathing characteristics and flexible framework structure, metal-organic framework (MOF) materials MIL-53(Fe), make promising nanocarrier for delivery applications. This work aimed to investigate the role of MIL-53(Fe) in the neovascularization of bone regeneration and the possible molecular mechanisms. The results validated that MIL-53(Fe) has excellent dispersion stability and biocompatibility. Angiogenic sprouting requires the activation of endothelial tip cells. By increasing the glycolytic activity of endothelial cells through self-assembling glucose, the nanocarrier MIL-53(Fe) markedly increased endothelial tip cell activation and boosted angiogenesis, ultimately encouraging bone repair. Through the Hippo/Yes-associated protein (YAP) pathway, the MIL-53(Fe)@Glucose complex was demonstrated to increase glycolytic activity and enhance activation of tip cell phenotype. This study demonstrated that the nanocarrier MIL-53(Fe) serves as an effective strategy for promoting rapid and sufficient angiogenesis during bone regeneration.

Indexed as

Endothelial CellsGlucoseMetal-Organic FrameworksNeovascularization, PhysiologicAngiogenesisAnimalsBone RegenerationGlycolysisHumansHuman Umbilical Vein Endothelial CellsYAP-Signaling ProteinsGlucoseMetal-Organic FrameworksYAP-Signaling ProteinsEndothelial tip cellGlycolysisHippo signalingMIL-53(Fe)Neovascularization

Identifiers

PMID40537794
PMCPMC12177960

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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.