Evidence map›Paper›PMID 38298451›Full record

ArticleBioactive materials2024

Heterogeneous DNA hydrogel loaded with Apt02 modified tetrahedral framework nucleic acid accelerated critical-size bone defect repair.

Yafei Han, Yan Wu, Fuxiao Wang, Guangfeng Li, Jian Wang, Xiang Wu, Anfu Deng, Xiaoxiang Ren, Xiuhui Wang, Jie Gao and 3 more

Open access · goldAbstract read
In one paragraph

Article in Bioactive materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
12.6field-weighted citation impact, top 1% 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

39 citing papers in PubMed, 54 citations in OpenAlex.

  1. Applications of DNA Hydrogels in Osteoporotic Bone Defects.Journal of functional biomaterials · 2026
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  20. Biocompatible Mesoporous Materials for Bone Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
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 at 2 institutions in 1 country.

Yafei HanOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Yan WuOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Fuxiao WangOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Guangfeng LiOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Jian WangOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Xiang WuOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Anfu DengOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Xiaoxiang RenOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Xiuhui WangOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Jie GaoSchool of Medicine, Shanghai University, Shanghai, 200444, China.
Zhongmin ShiNational Center for Orthopaedics, Shanghai Sixth People's Hospital, Shanghai, 200233, China.
Long BaiOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Jiacan SuOrganoid Research Center, Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.
Shanghai University · CNShanghai Sixth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Segmental bone defects, stemming from trauma, infection, and tumors, pose formidable clinical challenges. Traditional bone repair materials, such as autologous and allogeneic bone grafts, grapple with limitations including source scarcity and immune rejection risks. The advent of nucleic acid nanotechnology, particularly the use of DNA hydrogels in tissue engineering, presents a promising solution, attributed to their biocompatibility, biodegradability, and programmability. However, these hydrogels, typically hindered by high gelation temperatures (∼46 °C) and high construction costs, limit cell encapsulation and broader application. Our research introduces a novel polymer-modified DNA hydrogel, developed using nucleic acid nanotechnology, which gels at a more biocompatible temperature of 37 °C and is cost-effective. This hydrogel then incorporates tetrahedral Framework Nucleic Acid (tFNA) to enhance osteogenic mineralization. Furthermore, considering the modifiability of tFNA, we modified its chains with Aptamer02 (Apt02), an aptamer known to foster angiogenesis. This dual approach significantly accelerates osteogenic differentiation in bone marrow stromal cells (BMSCs) and angiogenesis in human umbilical vein endothelial cells (HUVECs), with cell sequencing confirming their targeting efficacy, respectively.

Indexed as

AngiogenesisAptamer02Bone regenerationDNA hydrogeltFNA

Identifiers

PMID38298451
PMCPMC10828543
OpenAlexW4390999271

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.