Evidence map›Paper›PMID 33322976›Full record

ArticleThe Journal of international medical research2020

Synergistic effects of miR-708-5p and miR-708-3p accelerate the progression of osteoporosis.

Ruran Wang, Yanhua Feng, Huaying Xu, Haoran Huang, Shan Zhao, Yuhong Wang, Hongyan Li, Jian Cao, Guoying Xu, Shengnan Huang

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Ruran WangDepartment of General Surgery, The Southern District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Yanhua FengHospital Infection Control Department, The Southern District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Huaying XuDepartment of General Surgery, The Southern District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Haoran HuangDepartment of General Surgery, The Southern District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Shan ZhaoDepartment of General Surgery, The Southern District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Yuhong WangSurgical Department, Xihongmen Hospital, Daxing District, Beijing, China.
Hongyan LiDepartment of General Surgery, The Southern District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Jian CaoCentral Laboratory, The Southern District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Guoying XuDepartment of General Surgery, The Southern District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Shengnan HuangPharmacy Department, The Southern District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0003-1099-120X
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBone homeostasis is a tightly orchestrated process maintained by osteoblasts and osteoclasts, and a disruption of their steady-state equilibrium can lead to the occurrence of osteoporosis (OP).

methodsWe investigated the differential expression of micro (mi)RNAs in the bone tissues of a postmenopausal osteoporosis rat model induced by ovariectomy (OVX). Real-time PCR was used to verify the differentially expressed miRNAs in bone samples from OP patients and controls. The specific targets of two differentially expressed miRNAs in osteogenic or osteoclast differentiation were determined by bioinformatic prediction, and mRNA and protein detection.

resultsmiR-708-5p and miR-708-3p were highly expressed in the bone tissue of OVX rats and OP patients. miR-708-5p negatively regulated osteoblast differentiation in bone marrow mesenchymal stem cells by targeting SMAD specific E3 ubiquitin protein ligase 2, while miR-708-3p positively regulated osteoclast differentiation in bone marrow monocytes by targeting cerebellar degeneration associated protein 1 antisense RNA. miR-708-5p and miR-708-3p were shown to originate from the same precursor miRNA and to have a synergistic effect on the development of osteoporosis with different temporal and spatial patterns.

conclusionOur findings provide a referential theoretical basis and targets for the prevention and treatment of osteoporosis.

Indexed as

MicroRNAsOsteoporosisAnimalsCell DifferentiationFemaleHumansOsteoblastsOsteogenesisRatsMicroRNAsMIRN708 microRNA, humandifferentiationmiR-708-3pmiR-708-5posteoblastsosteoclastsOsteoporosis

Identifiers

PMID33322976
PMCPMC7745577
OpenAlexW3112668797

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.