Evidence map›Paper›PMID 34020675›Full record

ArticleJournal of orthopaedic surgery and research2021

Neohesperidin promotes the osteogenic differentiation of bone mesenchymal stem cells by activating the Wnt/β-catenin signaling pathway.

Yue-Wen Chang, Wen-Jun Zhu, Wei Gu, Jun Sun, Zhi-Qiang Li, Xiao-En Wei

Open access · goldAbstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Nutraceuticals in osteoporosis prevention.Frontiers in nutrition · 2024
    Review
  4. Review
  5. 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 2 institutions in 1 country.

Yue-Wen Chang *Department of Orthopedics, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, No. 185, Puan Road, Huangpu District, Shanghai, 200021, China. chaxizhe19890715@163.com.
Wen-Jun Zhu *Department of Orthopedics, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, No. 185, Puan Road, Huangpu District, Shanghai, 200021, China.
Wei GuDepartment of Orthopedics, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, No. 185, Puan Road, Huangpu District, Shanghai, 200021, China.
Jun SunDepartment of Orthopedics, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, No. 185, Puan Road, Huangpu District, Shanghai, 200021, China.
Zhi-Qiang LiDepartment of Orthopedics, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, No. 185, Puan Road, Huangpu District, Shanghai, 200021, China.
Xiao-En WeiDepartment of Orthopedics, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, No. 185, Puan Road, Huangpu District, Shanghai, 200021, China.
Shuguang Hospital · CNShanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteoporosis is a common disease in aging populations. However, osteoporosis treatment is still challenging. Here, we aimed to investigate the role of neohesperidin (NEO) in osteoporosis progression and the potential mechanism.

methodsBone mesenchymal stem cells (BMSCs) were isolated and treated with different concentrations of NEO (0, 10, 30, 100 μM). Cell proliferation was analyzed by cell count kit-8 (CCK-8) assay. RNA-sequencing was performed on the isolated BMSCs with control and NEO treatment. Differentially expressed genes were obtained by R software. Alkaline phosphatase (ALP) staining and Alizarin red staining (ARS) were performed to assess the osteogenic capacity of the NEO. qRT-PCR was used to detect the expression of osteoblast markers. Western blot was used to evaluate the protein levels in BMSCs.

resultsNEO treatment significantly improved hBMSC proliferation at different time points, particularly when cells were incubated with 30 μM NEO (P < 0.05). NEO dose-dependently increased the ALP activity and calcium deposition than the control group (P < 0.05). A total of 855 differentially expressed genes were identified according to the significance criteria of log

conclusionNEO plays a positive role in promoting osteogenic differentiation of BMSCs, which was related with activation of Wnt/β-catenin pathway.

Indexed as

Alkaline Phosphatasebeta CateninBone and BonesCalciumCell DifferentiationCell ProliferationCells, CulturedDose-Response Relationship, DrugHesperidinHumansMesenchymal Stem CellsOsteogenesisOsteoporosisSignal TransductionWnt Signaling PathwayAlkaline Phosphatasebeta CateninCalciumHesperidinneohesperidinBone mesenchymal stem cellsNeohesperidinWnt/β-catenin pathway

Identifiers

PMID34020675
PMCPMC8139099
OpenAlexW3162380583

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.