Evidence map›Paper›PMID 31743606›Full record

ArticleFEBS open bio2020

Overexpression of RPN2 promotes osteogenic differentiation of hBMSCs through the JAK/STAT3 pathway.

Ling Ni, Jianhua Yu, Xueqiong Gui, Zhonghua Lu, Xiwen Wang, Hongyan Guo, Ying Zhou

RetractedOpen access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 32% 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, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. STAT3-mediated osteogenesis and osteoclastogenesis in osteoporosis.Cell communication and signaling : CCS · 2022
    Review
  5. Article
  6. Review
  7. Review
  8. Article
4 · The record

Corrections and comments

  • Retraction · 2023-03-17Euphemisms for Plagiarism · Investigation by Journal/Publisher · Investigation by Third Party · Plagiarism of Image · Unreliable Results and/or Conclusions ·
5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Ling NiDepartment of Geriatrics, Yangpu District Shidong Hospital, Shanghai, China.
Jianhua YuDepartment of Geriatrics, Yangpu District Shidong Hospital, Shanghai, China.
Xueqiong GuiDepartment of Geriatrics, Yangpu District Shidong Hospital, Shanghai, China.
Zhonghua LuDepartment of Geriatrics, Yangpu District Shidong Hospital, Shanghai, China.
Xiwen WangDepartment of Geriatrics, Yangpu District Shidong Hospital, Shanghai, China.
Hongyan GuoDepartment of Geriatrics, Yangpu District Shidong Hospital, Shanghai, China.
Ying ZhouDepartment of Geriatrics, Yangpu District Shidong Hospital, Shanghai, China.ORCID 0000-0001-7011-1716
YangPu Geriatric Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis is characterized by decreased bone mass and degenerating bone structure, which cause severe bone fragility and increase the risk for fractures. Human bone mesenchymal stem cells (hBMSCs) differentiate into osteoblasts through osteogenesis, and disturbances in the balance between bone generation and degeneration underlie the pathogenesis of senile osteoporosis. The highly conserved glycoprotein Ribophorin II (RPN2) is involved in multiple biological reactions, but the role of RPN2 in the osteogenic differentiation of hBMSCs and their molecular etiology is incompletely understood. Here, we show that RPN2 expression is up-regulated in hBMSCs during osteogenic differentiation. In vitro assays revealed that silencing of RPN2 inhibited hBMSC differentiation into osteoblasts. Moreover, RPN2 overexpression enhanced the expression of linked genes and resulted in high alkaline phosphatase activity. Our results suggest that RPN2 targets Janus kinase 1 (JAK1), and RPN2 overexpression was observed to induce JAK1 ubiquitination. Depletion of JAK1 facilitated osteogenic differentiation of RPN2-silenced hBMSCs. Moreover, western blot analysis revealed that RPN2 silencing suppressed the stimulation and nuclear translocation of the downstream signal transducer and activator of transcription 3 sensor; this could be reversed via RPN2 overexpression. This research sheds light on an innovative molecular mechanism that is associated with hBMSC differentiation into osteoblasts and may facilitate bone anabolism through RPN2.

Indexed as

Cell DifferentiationOsteogenesisCells, CulturedHexosyltransferasesHumansJanus Kinase 1Mesenchymal Stem CellsProteasome Endopeptidase ComplexSTAT3 Transcription FactorUbiquitinationHexosyltransferasesJAK1 protein, humanJanus Kinase 1Proteasome Endopeptidase ComplexRPN2 protein, humanSTAT3 protein, humanSTAT3 Transcription Factorbone mesenchymal stem cellhBMSCJAK/STAT3osteogenic differentiationRPN2

Identifiers

PMID31743606
PMCPMC6943221
OpenAlexW2989997954

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.