Evidence map›Paper›PMID 29488053›Full record

ArticleInflammation2018

miR-140-5p/miR-149 Affects Chondrocyte Proliferation, Apoptosis, and Autophagy by Targeting FUT1 in Osteoarthritis.

Zi Wang, Jialei Hu, Yue Pan, Yujia Shan, Liqun Jiang, Xia Qi, Li Jia

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
11.7field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Role of MiRNA in the Regulation of Blood Group Expression.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2024
    Review
  8. Article
  9. Review
  10. The Role of MicroRNAs in the Pathophysiology of Osteoarthritis.International journal of molecular sciences · 2024
    Review
  11. Review
  12. Article
  13. Chondrocyte autophagy mechanism and therapeutic prospects in osteoarthritis.Frontiers in cell and developmental biology · 2024
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Zi WangCollege of Laboratory Medicine, Dalian Medical University, 9 Lushunnan Road Xiduan, Dalian, Liaoning Province, 116044, China.
Jialei HuCollege of Laboratory Medicine, Dalian Medical University, 9 Lushunnan Road Xiduan, Dalian, Liaoning Province, 116044, China.
Yue PanCollege of Laboratory Medicine, Dalian Medical University, 9 Lushunnan Road Xiduan, Dalian, Liaoning Province, 116044, China.
Yujia ShanCollege of Laboratory Medicine, Dalian Medical University, 9 Lushunnan Road Xiduan, Dalian, Liaoning Province, 116044, China.
Liqun JiangGraduate School, Dalian Medical University, Dalian, Liaoning Province, 116044, China.
Xia QiCollege of Laboratory Medicine, Dalian Medical University, 9 Lushunnan Road Xiduan, Dalian, Liaoning Province, 116044, China.
Li JiaCollege of Laboratory Medicine, Dalian Medical University, 9 Lushunnan Road Xiduan, Dalian, Liaoning Province, 116044, China. jiali0386@sina.com.ORCID http://orcid.org/0000-0002-9924-0439
Dalian Medical University · CN

Funding

National Natural Science Foundation of China 81472014
6 · The paper itself

Abstract

Osteoarthritis (OA), the most prevalent chronic and degenerative joint disease, is characterized by articular cartilage degradation and chondrocyte injury. Increased cell apoptosis and defective cell autophagy in chondrocytes are a feature of degenerative cartilage. MicroRNAs (miRNAs) have been identified as potential regulators of OA. This study aimed to determine the potential role of miR-140-5p and miR-149 in apoptosis, autophagy, and proliferation in human primary chondrocytes and investigate the underlying mechanism. We revealed the differential expressional profiles of miR-140-5p/149 and fucosyltransferase 1 (FUT1) in the articular cartilage tissues of OA patients and normal people and validated FUT1 was a direct target of miR-140-5p/149. The overexpression of miR-140-5p/149 inhibited apoptosis and promoted proliferation and autophagy of human primary chondrocytes via downregulating FUT1. On the contrary, the downregulation of miR-140-5p/149 inhibited chondrocyte proliferation and autophagy, whereas the effect was reversed by FUT1 knockdown. Taken together, our data suggested that miR-140-5p and miR-149 could mediate the development of OA, which was regulated by FUT1. miR-140-5p/miR-149/FUT1 axis might serve as a predictive biomarker and a potential therapeutic target in OA treatment.

Indexed as

ApoptosisAutophagyCell ProliferationChondrocytesFucosyltransferasesGalactoside 2-alpha-L-fucosyltransferaseHumansMicroRNAsOsteoarthritisFucosyltransferasesGalactoside 2-alpha-L-fucosyltransferaseMicroRNAsMirn140 microRNA, humanMIRN149 microRNA, humanapoptosisautophagyFUT1miRNAsosteoarthritisproliferation

Identifiers

PMID29488053
OpenAlexW2787906815

What OpenQuestion holds

Textmetadata
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.