Evidence map›Paper›PMID 27860183›Full record

ArticleJournal of cellular and molecular medicine2017

MicroRNA-98 regulates osteogenic differentiation of human bone mesenchymal stromal cells by targeting BMP2.

Guo-Ping Zhang, Jing Zhang, Chao-Hua Zhu, Lei Lin, Jian Wang, Hai-Jing Zhang, Jun Li, Xiao-Guang Yu, Zhen-Shuan Zhao, Wei Dong and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 38 citations in OpenAlex.

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  6. MicroRNA-loaded biomaterials for osteogenesis.Frontiers in bioengineering and biotechnology · 2022
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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

11 authors at 2 institutions in 1 country.

Guo-Ping ZhangDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Jing ZhangMedical Physics Department of Basic Medical College of Hebei Medical University, Shijiazhuang, China.
Chao-Hua ZhuDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Lei LinDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Jian WangDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Hai-Jing ZhangDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Jun LiDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Xiao-Guang YuDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Zhen-Shuan ZhaoDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Wei DongDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Guo-Bin LiuDepartment of Orthopedics, The First Hospital of Hebei Medical University, Shijiazhuang, China.
First Affiliated Hospital of Hebei Medical University · CNHebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To study the effects of microRNA-98 (miR-98) on human bone mesenchymal stromal cells (hBMSCs). The patients undergoing hip arthroplasty were selected by inclusion/exclusion criteria for this study. The extracted hBMSCs were detected of osteogenic differentiation by alizarin red S staining, and of cell phenotype by flow cytometry. Bioinformatics, dual luciferase report, western blotting, RT-PCR and immunoblotting were used in our study. The hBMSCs were divided into miR-98 mimics, miR-98 negative control (NC), miR-98 inhibitors, Mock and miR-98 inhibitors + siBMP2 groups. Human bone mesenchymal stromal cells were extracted and purified in vitro and had specific cytological morphology, surface markers and abilities of self-renewal and differentiation. Compared with the NC group and Mock group, the miR-98 mimics group showed increased miR-98 level while the miR-98 inhibitors group decreased miR-98 level (both P < 0.01). Dual luciferase reporter showed BMP2 was the target gene of miR-98. The levels of mRNA and protein expression of BMP2, protein expression of RUNX2, alkaline phosphatase activity and osteocalcin content significantly decreased in the miR-98 mimics group while increased in the miR-98 inhibitors group and showed no changes in the NC group and Mock group (all P < 0.05). The miR-98 mimics group showed obviously declined stained red particles and the miR-98 inhibitors group showed opposite result. After lowering the expression of miR-98, osteogenic differentiation ability of hBMSCs rose, which was weakened by the transfection with siBMP2. miR-98 may regulate osteogenic differentiation of hBMSCs by targeting BMP2.

Indexed as

Base SequenceBiomarkersBone Marrow CellsBone Morphogenetic Protein 2CalciumCell DifferentiationCell ShapeFemaleHumansLuciferasesMaleMesenchymal Stem CellsMicroRNAsMiddle AgedOsteogenesisReproducibility of ResultsBiomarkersBMP2 protein, humanBone Morphogenetic Protein 2CalciumLuciferasesMicroRNAsMIRN98 microRNA, humanbone morphogenetic protein-2human bone mesenchymal stromal cellsmicroRNAmicroRNA-98osteogenic differentiationsignal pathwaytranscriptiontranslation

Identifiers

PMID27860183
PMCPMC5264139
OpenAlexW2555729175

What OpenQuestion holds

Textmetadata
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.