Evidence map›Paper›PMID 31732956›Full record

ArticleIn vitro cellular & developmental biology. Animal2020

miR-140-3p exhibits repressive functions on preosteoblast viability and differentiation by downregulating MCF2L in osteoporosis.

Jin-He Mao, Yu-Xin Sui, Shuang Ao, Yu Wang, Yu Liu, Hui Leng

Abstract read
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In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. miR-140-5p and miR-140-3p: Key Actors in Aging-Related Diseases?International journal of molecular sciences · 2022
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. The Role of MicroRNAs in Bone Metabolism and Disease.International journal of molecular sciences · 2020
    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

6 authors at 1 institution in 1 country.

Jin-He MaoDepartment of Orthopedics, Chifeng Municipal Hospital, No.1 Zhaowuda Road, Chifeng, 024000, Inner Mongolia, People's Republic of China.
Yu-Xin SuiDepartment of Orthopedics, Chifeng Municipal Hospital, No.1 Zhaowuda Road, Chifeng, 024000, Inner Mongolia, People's Republic of China.
Shuang AoDepartment of Orthopedics, Chifeng Municipal Hospital, No.1 Zhaowuda Road, Chifeng, 024000, Inner Mongolia, People's Republic of China.
Yu WangDepartment of Orthopedics, Chifeng Municipal Hospital, No.1 Zhaowuda Road, Chifeng, 024000, Inner Mongolia, People's Republic of China.
Yu LiuDepartment of Orthopedics, Chifeng Municipal Hospital, No.1 Zhaowuda Road, Chifeng, 024000, Inner Mongolia, People's Republic of China.
Hui LengDepartment of Orthopedics, Chifeng Municipal Hospital, No.1 Zhaowuda Road, Chifeng, 024000, Inner Mongolia, People's Republic of China. cflh33388@163.com.
Chifeng Municipal Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous research manifested that miR-140-3p was a latent biomarker for osteoporosis. Nevertheless, the mechanism of miR-140-3p in osteoporosis is still not clear and needs ulteriorly studying. The purpose of our paper was to ulteriorly probe the underlying mechanism of miR-140-3p on osteoporosis. Firstly, based on the data acquired from GEO database, we found that miR-140-3p was highly expressed; meanwhile, MCF2L was lowly expressed in osteoporosis patients. Upregulation/downregulation of miR-140-3p by miR-140-3p mimic/inhibitor restrained/promoted MC3T3-E1 cell viability and differentiation. However, miR-140-3p over-expression/downregulation accelerated/repressed MC3T3-E1 cell apoptosis. MCF2L was forecasted as a target of miR-140-3p by miRanda, miRWalk, and TargetScan miRNA target gene prediction software. Luciferase reporter assay confirmed that MCF2L could be directly targeted by miR-140-3p. Moreover, we identified that the expression of MCF2L was negatively regulated by miR-140-3p. From rescue assays, we discovered that knockdown of MCF2L weakened the promoting influence of miR-140-3p ablation on MC3T3-E1 cell viability and differentiation, and receded the suppressing impact of miR-140-3p reduction on MC3T3-E1 cell apoptosis. Above all, this research disclosed that miR-140-3p repressed preosteoblast viability and differentiation while promoted preosteoblast apoptosis via targeting MCF2L. Our discoveries might afford a theoretical basis of developing a latent novel target for osteoporosis therapy.

Indexed as

Alkaline PhosphataseAnimalsApoptosisBase SequenceCell DifferentiationCell LineCell SurvivalCore Binding Factor Alpha 1 SubunitDown-RegulationHumansMiceMicroRNAsOsteoblastsOsteoporosisRho Guanine Nucleotide Exchange FactorsSp7 Transcription FactorAlkaline PhosphataseCore Binding Factor Alpha 1 SubunitMCF2L protein, humanMcf2l protein, mouseMicroRNAsMirn140 microRNA, humanMIRN140 microRNA, mouseRho Guanine Nucleotide Exchange FactorsSp7 protein, mouseSp7 Transcription FactorApoptosisDifferentiationMCF2LmiR-140-3pOsteoporosisViability

Identifiers

PMID31732956
OpenAlexW2985372365

What OpenQuestion holds

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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.