Evidence map›Paper›PMID 34783166›Full record

ArticleJournal of cellular and molecular medicine2021

Gentiopicroside promotes the osteogenesis of bone mesenchymal stem cells by modulation of β-catenin-BMP2 signalling pathway.

Huaji Jiang, Jialiang Zhong, Wenjun Li, Jianghui Dong, Cory J Xian, Yung-Kang Shen, Lufeng Yao, Qiang Wu, Liping Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
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  7. Article
  8. Article
  9. Review
  10. Regulatory mechanisms of Gentiopicroside on human diseases: a brief review.Naunyn-Schmiedeberg's archives of pharmacology · 2024
    Review
  11. Review
  12. Article
  13. 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

9 authors at 5 institutions in 3 countries.

Huaji JiangDepartment of Orthopaedic, Yuebei People's Hospital Affiliated to Medical College of Shantou University, Shaoguan, China.
Jialiang ZhongDepartment of Clinical Laboratory, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Wenjun LiDepartment of Orthopaedic, Yuebei People's Hospital Affiliated to Medical College of Shantou University, Shaoguan, China.
Jianghui DongUniSA Clinical& Health Sciences, University of South Australia, Adelaide, SA, Australia.ORCID 0000-0003-3961-1688
Cory J XianUniSA Clinical& Health Sciences, University of South Australia, Adelaide, SA, Australia.
Yung-Kang ShenSchool of Dental Technology, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
Lufeng YaoDepartment of Foot and Ankle Surgery, Ningbo No. 6 Hospital, Ningbo, China.
Qiang WuDepartment of Orthopaedic, Yuebei People's Hospital Affiliated to Medical College of Shantou University, Shaoguan, China.
Liping WangUniSA Clinical& Health Sciences, University of South Australia, Adelaide, SA, Australia.ORCID 0000-0001-9355-1167
Shantou University · CNUniversity of South Australia · AUNingbo No.6 Hospital · CNSun Yat-sen University · CNTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis is characterized by increased bone fragility, and the drugs used at present to treat osteoporosis can cause adverse reactions. Gentiopicroside (GEN), a class of natural compounds with numerous biological activities such as anti-resorptive properties and protective effects against bone loss. Therefore, the aim of this work was to explore the effect of GEN on bone mesenchymal stem cells (BMSCs) osteogenesis for a potential osteoporosis therapy. In vitro, BMSCs were exposed to GEN at different doses for 2 weeks, whereas in vivo, ovariectomized osteoporosis was established in mice and the therapeutic effect of GEN was evaluated for 3 months. Our results in vitro showed that GEN promoted the activity of alkaline phosphatase, increased the calcified nodules in BMSCs and up-regulated the osteogenic factors (Runx2, OSX, OCN, OPN and BMP2). In vivo, GEN promoted the expression of Runx2, OCN and BMP2, increased the level of osteogenic parameters, and accelerated the osteogenesis of BMSCs by activating the BMP pathway and Wnt/β-catenin pathway, effect that was inhibited using the BMP inhibitor Noggin and Wnt/β-catenin inhibitor DKK1. Silencing the β-catenin gene and BMP2 gene blocked the osteogenic differentiation induced by GEN in BMSCs. This block was also observed when only β-catenin was silenced, although the knockout of BMP2 did not affect β-catenin expression induced by GEN. Therefore, GEN promotes BMSC osteogenesis by regulating β-catenin-BMP signalling, providing a novel strategy in the treatment of osteoporosis.

Indexed as

Animalsbeta CateninBone and BonesBone Morphogenetic Protein 2Cell DifferentiationCells, CulturedFemaleIridoid GlucosidesMesenchymal Stem CellsMiceMice, Inbred C57BLOsteogenesisOsteoporosisRecombinant ProteinsSignal TransductionTransforming Growth Factor betabeta CateninBone Morphogenetic Protein 2gentiopicrosideIridoid Glucosidesrecombinant human bone morphogenetic protein-2Recombinant ProteinsTransforming Growth Factor betaBMP pathwayGentiopicrosideosteogenic factorsosteogenic parametersosteoporosisWnt/β-catenin pathway

Identifiers

PMID34783166
PMCPMC8642693
OpenAlexW3213872098

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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.