Evidence map›Paper›PMID 32871042›Full record

ArticleJournal of cellular and molecular medicine2020

microRNA-148a-3p in extracellular vesicles derived from bone marrow mesenchymal stem cells suppresses SMURF1 to prevent osteonecrosis of femoral head.

Shengxiang Huang, Yaochun Li, Panfeng Wu, Yongbing Xiao, Ningbo Duan, Jing Quan, Wei Du

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Surgical suction filter-derived bone graft displays osteogenic miRNA and mRNA patterns.European journal of trauma and emergency surgery : official publication of the European Trauma Society · 2024
    Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

Shengxiang HuangDepartment of Orthopedics, Hunan Children's Hospital, Changsha, China.ORCID 0000-0002-8327-1660
Yaochun LiDepartment of Rehabilitation, Xiangya Hospital of Central South University, Changsha, China.ORCID 0000-0002-8723-0938
Panfeng WuDepartment of Orthopedics, Xiangya Hospital of Central South University, Changsha, China.ORCID 0000-0002-9280-887X
Yongbing XiaoDepartment of Orthopedics, Xiangya Hospital of Central South University, Changsha, China.ORCID 0000-0002-4666-6911
Ningbo DuanDepartment of Rehabilitation, Xiangya Hospital of Central South University, Changsha, China.ORCID 0000-0001-5110-6313
Jing QuanDepartment of Rehabilitation, Xiangya Hospital of Central South University, Changsha, China.ORCID 0000-0002-3986-5189
Wei DuDepartment of Rehabilitation, Xiangya Hospital of Central South University, Changsha, China.ORCID 0000-0002-8425-4088
Central South University · CNHunan Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicle (EV)-associated microRNAs (miRNAs) have been found as the important biomarkers participating in the development of osteonecrosis of the femoral head (ONFH). Consequently, this study sought to examine the underlying mechanism of bone marrow mesenchymal stem cell (BMSC)-derived EVs containing miR-148a-3p in ONFH. The ONFH rat models were established. Reverse transcription quantitative polymerase chain reaction (RT-qPCR) and Western blot analysis were applied to detect miR-148a-3p, Smad ubiquitination regulatory factor 1 (SMURF1), SMAD7 and B-cell CLL/lymphoma 2 (BCL2) expression, followed by determination of relationship between miR-148a-3p and SMURF1. BMSCs were isolated from normal rats and ONFH rats, and EVs were extracted from BMSCs of normal rats. BMSCs from ONFH rats were treated with mimic, inhibitor, small interfering RNA or EVs from miR-148a-3p mimic-treated BMSCs from normal rats (BMSC-EV-miR-148a-3p mimic). Cell Counting Kit-8 and alizarin red staining were utilized to detect cell viability and osteogenic differentiation of BMSCs. ONFH rats were injected with BMSC-EV-miR-148a-3p mimic to explore the function of BMSC-EV-delivered miR-148a-3p in vivo. miR-148a-3p was down-regulated in BMSCs and EVs from ONFH rats following decreased BMSCs viability and osteogenic differentiation. SMURF1 was a target gene of miR-148a-3p, and resulted in ubiquitination and degradation of SMAD7 to decreased BCL2 expression. The proliferation and differentiation of BMSCs were promoted by BMSC-EV-miR-148a-3p mimic or SMURF1 silencing. Additionally, BMSC-EV-miR-148a-3p mimic increased cell proliferation and osteogenic response, diminished SMURF1 expression, and elevated SMAD7 and BCL2 expression in ONFH rats. Collectively, miR-148a-3p overexpressed in BMSC-EVs promoted SMAD7 and BCL2 expression by inhibiting SMURF1, thus alleviating ONFH.

Indexed as

AnimalsCell DifferentiationCell ProliferationCell SurvivalDisease Models, AnimalExtracellular VesiclesFemaleFemur Head NecrosisHEK293 CellsHumansMaleMesenchymal Stem CellsMicroRNAsOsteogenesisProto-Oncogene Proteins c-bcl-2Rats, Sprague-DawleyMicroRNAsMIRN148a microRNA, ratProto-Oncogene Proteins c-bcl-2Smad7 ProteinSmurf1 protein, ratUbiquitin-Protein LigasesBCL2bone marrow mesenchymal stem cellsextracellular vesiclesmicroRNA-148a-3posteonecrosis of the Femeral HeadSMAD7SMURF1

Identifiers

PMID32871042
PMCPMC7576243
OpenAlexW3082749778

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.