Evidence map›Paper›PMID 32404197›Full record

ArticleBMC musculoskeletal disorders2020

MicroRNA-532-5p is implicated in the regulation of osteoporosis by forkhead box O1 and osteoblast differentiation.

Xinyu Guo, Shijun Wei, Feng Xu, Xianhua Cai, Huasong Wang, Ran Ding

Open access · goldAbstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 27% 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, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Common miRNAs of Osteoporosis and Fibromyalgia: A Review.International journal of molecular sciences · 2023
    Review
  4. Review
  5. Article
  6. The Potential Role of miRNAs in Cognitive Frailty.Frontiers in aging neuroscience · 2021
    Review
  7. Article
  8. Article
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 2 institutions in 1 country.

Xinyu GuoDepartment of Orthopaedics, Guizhou Provincial Orthopaedic Hospital, Guiyang City, Guizhou Province, 550002, PR China.
Shijun WeiOrthopedic surgery of Wuhan General Hospital of People's Liberation Army, No.627 Wuluo Road, Wuhan City, Hubei Province, 430000, PR China.
Feng XuOrthopedic surgery of Wuhan General Hospital of People's Liberation Army, No.627 Wuluo Road, Wuhan City, Hubei Province, 430000, PR China.
Xianhua CaiOrthopedic surgery of Wuhan General Hospital of People's Liberation Army, No.627 Wuluo Road, Wuhan City, Hubei Province, 430000, PR China.
Huasong WangOrthopedic surgery of Wuhan General Hospital of People's Liberation Army, No.627 Wuluo Road, Wuhan City, Hubei Province, 430000, PR China.
Ran DingOrthopedic surgery of Wuhan General Hospital of People's Liberation Army, No.627 Wuluo Road, Wuhan City, Hubei Province, 430000, PR China. ct2410@163.com.
Wuhan General Hospital of Guangzhou · CNGuizhou Provincial People's Hospital · CN

Funding

Hubei Provincial Population and Family Planning Commission WJ2017M155
6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) are critical regulators in osteogenesis and cartilage formation. This study was designed to investigate whether miR-532-5p plays a role in the regulation of osteoporosis.

methodsOsteoporotic fractures (OP group, n = 10) or osteoarthritis without osteoporosis (control group, n = 10) were selected as subjects in this study. Quantitative analysis of gene expression was performed by RT-PCR. Western blot was used to determine the expression levels of protein forkhead O1 (FOXO1). Bioinformatics analyses and luciferase reporter assay were used to verify the downstream target of miR-532-5p.

resultsCompared with the non-osteoporotic controls, miR-532-5p was upregulated in osteoporotic samples, and expression of miR-532-5p was downregulated in the osteogenic C2C12 cell model. Overexpression of miR-532-5p resulted in decreased expression levels of key osteoblast markers, including alkaline phosphatase (ALP), osteocalcin (OC), and collagen type I alpha 1 (COL1A1). The inhibitory results of miR-532-5p were reversed. MiR-532-5p contained a putative FOXO1 binding site. Moreover, miR-532-5p inhibited the expression of FOXO1, and overexpression of FOXO1 inhibited the effect of miR-532-5p on osteoblast markers.

conclusionsMiR-532-5p can provide references to osteoporosis by regulating the expression of FOXO1 and osteoblast differentiation. MiR-532-5p might serve as a therapeutic target for osteoporosis.

Indexed as

AgedAlkaline PhosphataseCell DifferentiationCell LineCollagen Type ICollagen Type I, alpha 1 ChainFemaleForkhead Box Protein O1HumansMicroRNAsMiddle AgedOsteoblastsOsteocalcinOsteogenesisOsteoporosisTransfectionAlkaline PhosphataseBGLAP protein, humanCOL1A1 protein, humanCollagen Type ICollagen Type I, alpha 1 ChainForkhead Box Protein O1FOXO1 protein, humanMicroRNAsMIRN532 microRNA, humanOsteocalcinFOXO1miR-532-5pOsteogenic differentiationOsteoporosis

Identifiers

PMID32404197
PMCPMC7218624
OpenAlexW3028036412

What OpenQuestion holds

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LicenceCC BY
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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.