Evidence map›Paper›PMID 29073887›Full record

ArticleBMC musculoskeletal disorders2017

Effects of Osteoglycin (OGN) on treating senile osteoporosis by regulating MSCs.

Xia Chen, Junsong Chen, Dongliang Xu, Shuangxia Zhao, Huaidong Song, Yongde Peng

Open access · goldAbstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 30% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Osteoglycin and Bone-a Systematic Review.Current osteoporosis reports · 2019
    Pooled it
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  3. Article
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  5. Article
  6. Article
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  8. Article
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  11. miR-21 regulates osteogenic and adipogenic differentiation of BMSCs by targeting PTEN.Journal of musculoskeletal & neuronal interactions · 2021
    Article
  12. Article
  13. The Pathophysiology of Osteoporosis after Spinal Cord Injury.International journal of molecular sciences · 2021
    Review
  14. Review
  15. Article
  16. 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 3 institutions in 1 country.

Xia ChenDepartment of Endocrinology and Metabolism, Shanghai General Hospital of Nanjing Medical University, 100 Haining Road, Shanghai, 200080, China.
Junsong ChenKey Laboratory of Systems Biomedicine(Ministry of Education), Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
Dongliang XuDepartment of Urology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, 100 Haining Road, Shanghai, Shanghai, 200080, China.
Shuangxia ZhaoShanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, No. 639 zhizaoju Road, Shanghai, China.
Huaidong SongShanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, No. 639 zhizaoju Road, Shanghai, China.
Yongde PengDepartment of Endocrinology and Metabolism, Shanghai General Hospital of Nanjing Medical University, 100 Haining Road, Shanghai, 200080, China. pengyongde0909@126.com.
Shanghai First People's Hospital · CNShanghai Ninth People's Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSignificant amount of bone mass is lost during the process of aging due to an imbalance between osteoblast-mediated bone formation and osteoclast-mediated bone resorption in bone marrow microenvironment, which leads to net bone loss in the aging population, resulting in the pathogenesis of osteoporosis.

methodsFirstly, differences in proliferative capacity of adipocyte or adipogenic differentiation in mouse mesenchymal stem cells (MMSCs) and senile mouse model-derived bone marrow mesenchymal stem cells (SMMSCs), as well as mRNA expression of OGN and PPARγ2 were observed. Secondly, osteogenic abilities of MMSCs and SMMSCs treated with rosiglitazone (a PPARγ2 agonist) to induce osteogenic changes were observed, and negative correlation of PPARγ2 with OGN was evaluated. Thirdly, the role of SMMSCs in promoting osteogenesis was examined through enhancing expression of OGN; besides, the related mechanism was investigated by means of expression of related adipocyte and osteoblast specific genes.

resultsForced OGN expression by OGN-infected lentivirus could increase expression of Wnt5b, RUNX2, OCN, ALP and Colla1, as well as bone formation, while decreases expression of adipogenesis marker PPARγ2. It resulted in expression inhibition of adipocyte genes such as adipocytic differentiation related genes adipocyte binding protein 2 (aP2) and osteoclast differentiation factor Rankl in bone marrow, giving rise to increased bone mass.

conclusionOGN may plays a significant role in osteoporosis, which may also provide a potential target for therapeutic intervention of senile osteoporosis characterized by altered differentiation of BMSCs into osteoblasts and adipocytes.

Indexed as

AdipogenesisAnimalsDrug Evaluation, PreclinicalFemaleHEK293 CellsHumansIntercellular Signaling Peptides and ProteinsMesenchymal Stem CellsMice, Inbred C57BLOsteogenesisOsteoporosisPPAR gammaPrimary Cell CultureRosiglitazoneThiazolidinedionesIntercellular Signaling Peptides and ProteinsOGN protein, humanPPAR gammaRosiglitazoneThiazolidinedionesAdipogenesisMesenchymal stromal cellsOsteoblastogenesisOsteoglycinPeroxisome proliferators-activated receptor-γ 2Senile osteoporosis

Identifiers

PMID29073887
PMCPMC5658998
OpenAlexW2766527903

What OpenQuestion holds

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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.