Evidence map›Paper›PMID 32877980›Full record

ArticleJournal of musculoskeletal & neuronal interactions2020

MiR-214 regulates fracture healing through inhibiting Sox4 and its mechanism.

Zhaoxu Xin, Defu Cai, Jingchun Wang, Lin Ma, Fuguo Shen, Can Tang, Lihui Hu, Wencai Sun

Open access · greenAbstract read
In one paragraph

Article in Journal of musculoskeletal & neuronal interactions, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. 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

8 authors at 1 institution in 1 country.

Zhaoxu XinDepartment of Orthopaedics, The Third Affiliated Hospital of Qiqihar Medical University, P.R. China.
Defu CaiInstitute of Pharmaceutical Sciences, Qiqihar Medical University, P.R. China.
Jingchun WangDepartment of Personnel, Qiqihar Medical University, P.R. China.
Lin MaDepartment of Orthopaedics, The Third Affiliated Hospital of Qiqihar Medical University, P.R. China.
Fuguo ShenDepartment of Orthopaedics, The Third Affiliated Hospital of Qiqihar Medical University, P.R. China.
Can TangDepartment of Orthopaedics, The Third Affiliated Hospital of Qiqihar Medical University, P.R. China.
Lihui HuDepartment of Orthopaedics, The Third Affiliated Hospital of Qiqihar Medical University, P.R. China.
Wencai SunDepartment of Orthopaedics, The Third Affiliated Hospital of Qiqihar Medical University, P.R. China.
Qiqihar Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the expression of micro ribonucleic acid (miR)-214 in the bone tissue and blood of patients with fragility fracture.

methodsThe expression of miR-214 was detected via quantitative reverse transcription-polymerase chain reaction. The effect of miR-214 on proliferation and apoptosis of osteoblasts were detected via methyl thiazolyl tetrazolium assay and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling staining.

resultsThe expression of miR-214 in the bone tissue and blood of patients with fragility fracture significantly declined. miR-214 could promote the proliferation of osteoblasts and inhibited the apoptosis of osteoblasts. miR-214 is involved in fracture healing through inhibiting Sox4 and promoting phosphorylation of PI3K/AKT pathway. The expression of BSP in cells treated with miR-214 mimics was significantly increased to 2.5-fold (p=0.0168), while the expression of BSP in cells treated with miR-214 AMO was significantly decreased, reduced to 0.3 times (p=0.0397). The expression of BMP2 in cells treated with miR-214 mimics was significantly increased to 2.5-fold (p=0.003), while the expression of BMP2 was significantly decreased in cells treated with miR-214 AMO, reduced to 0.3 times (p=0.0002). miR-214 can regulate the expression of Sox2, PI3K and AKT proteins.

conclusionMiR-214 regulates the proliferation, apoptosis, bone formation of osteoblasts and participate in the fracture healing process by inhibiting the expression of Sox4, which provided new ideas for clinical treatment of fracture healing.

Indexed as

AdultAgedAged, 80 and overApoptosisCell ProliferationCells, CulturedFemaleFracture HealingGene Expression RegulationHumansMaleMicroRNAsMiddle AgedOsteoblastsOsteogenesisOsteoporotic FracturesMicroRNAsMIRN214 microRNA, humanSOX4 protein, humanSOXC Transcription FactorsApoptosismiR-214OsteoblastsProliferationSox4

Identifiers

PMID32877980
PMCPMC7493443
OpenAlexW3083500127

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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 Socratic graph.