Evidence map›Paper›PMID 29686962›Full record

ArticleAnalytical cellular pathology (Amsterdam)2018

MicroRNA-378 Promotes Osteogenesis-Angiogenesis Coupling in BMMSCs for Potential Bone Regeneration.

Bo Zhang, Yali Li, Yang Yu, Jinlong Zhao, Yangzhen Ou, Yu Chao, Binhui Yang, Xiaorui Yu

Open access · goldAbstract read
In one paragraph

Article in Analytical cellular pathology (Amsterdam), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Co-regulation of circadian clock genes and microRNAs in bone metabolism.Journal of Zhejiang University. Science. B · 2022
    Review
  3. Article
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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

8 authors at 1 institution in 1 country.

Bo ZhangDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.
Yali Li3201 Hospital Affiliated to Xi'an Jiaotong University, Hanzhong, Shaanxi 723000, China.
Yang Yu3201 Hospital Affiliated to Xi'an Jiaotong University, Hanzhong, Shaanxi 723000, China.
Jinlong Zhao3201 Hospital Affiliated to Xi'an Jiaotong University, Hanzhong, Shaanxi 723000, China.
Yangzhen Ou3201 Hospital Affiliated to Xi'an Jiaotong University, Hanzhong, Shaanxi 723000, China.
Yu ChaoDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.
Binhui Yang3201 Hospital Affiliated to Xi'an Jiaotong University, Hanzhong, Shaanxi 723000, China.ORCID 0000-0001-6742-8093
Xiaorui YuDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.ORCID 0000-0003-3230-2583
Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone tissue regeneration was closely associated with osteogenesis and angiogenesis. The harmonious regulation of osteogenetic and angiogenic growth factors would enhance bone regeneration, while the imbalance of that would lead to local excessive bone formation or vascular mass due to exogenous delivery. Therefore, microRNA is believed to regulate multiple metabolism progress through endogenous signaling pathways on the gene level. In this work, we identified microRNA 378 as a positive regulator of osteogenesis and angiogenesis simultaneously and also observed an increase of microRNA 378 than control in human bone marrow mesenchymal stem cells (hBMMSCs) after osteoblast induction. Besides, osteogenetic and angiogenic gene expression increased simultaneously after overexpression of microRNA 378. Moreover, alizarin red staining and alkaline phosphatase (ALP) staining enhanced, and secretion of vascular endothelial growth factor (VEGF) increased. In this way, we believed miR378 was an ideal target to osteogenesis-angiogenesis coupling for bone regeneration, which provides a potential tool for the gene therapy of bone regeneration.

Indexed as

AnimalsBiomarkersBone RegenerationCell DifferentiationCell LineCells, CulturedHumansHuman Umbilical Vein Endothelial CellsMesenchymal Stem CellsMiceMicroRNAsNeovascularization, PhysiologicOsteogenesisVascular Endothelial Growth Factor ABiomarkersMicroRNAsMIRN378 microRNA, humanVascular Endothelial Growth Factor A

Identifiers

PMID29686962
PMCPMC5852880
OpenAlexW2794424700

What OpenQuestion holds

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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.