Evidence map›Paper›PMID 29907764›Full record

ArticleCell death & disease2018

Long non-coding RNA HOTAIR promotes osteoarthritis progression via miR-17-5p/FUT2/β-catenin axis.

Jialei Hu, Zi Wang, Yujia Shan, Yue Pan, Jia Ma, Li Jia

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

80 citing papers in PubMed, 128 citations in OpenAlex.

  1. Review
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  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Long noncoding RNACell cycle (Georgetown, Tex.) · 2023
    Article
  20. Review

20 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Jialei Hu *College of Laboratory Medicine, Dalian Medical University, Dalian, Liaoning Province, 116044, China.
Zi Wang *Department of Sports Medicine, Dalian Municipal Central Hospital, Dalian, Liaoning Province, 116033, China.
Yujia ShanCollege of Laboratory Medicine, Dalian Medical University, Dalian, Liaoning Province, 116044, China.
Yue PanCollege of Laboratory Medicine, Dalian Medical University, Dalian, Liaoning Province, 116044, China.
Jia MaCollege of Laboratory Medicine, Dalian Medical University, Dalian, Liaoning Province, 116044, China.
Li JiaCollege of Laboratory Medicine, Dalian Medical University, Dalian, Liaoning Province, 116044, China. jiali0386@sina.com.ORCID http://orcid.org/0000-0003-3152-3253
Dalian Medical University · CNDalian Municipal Central Hospital · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81772277
6 · The paper itself

Abstract

Osteoarthritis (OA) is a chronic joint disease and hard to cure at present. Accumulating evidence suggests long noncoding RNA-HOTAIR (lncRNA-HOTAIR) plays important role in OA progression. However, the underlying molecular mechanism of HOTAIR in OA progression has not been well elucidated. In the present study, we identified that HOTAIR level was upregulated in OA cartilage tissues. High expression of HOTAIR was correlated with modified Mankin scale, extracellular matrix (ECM) degradation and chondrocytes apoptosis. The expression of miR-17-5p was down-regulated, while alpha-1, 2 fucosyltransferase 2 (FUT2) was increased in OA progression. Luciferase reporter and RNA immunoprecipitation (RIP) assays indicated that HOTAIR could directly bind to miR-17-5p and indirectly upregulate FUT2 level. Functional investigation revealed HOTAIR and FUT2 aggravated ECM degradation and chondrocytes apoptosis, and this effect could be reversed by miR-17-5p. Altered FUT2 modulated the activity of wnt/β-catenin pathway and HOTAIR/miR-17-5p also mediated wnt/β-catenin pathway through FUT2. Collectively, our findings indicated that HOTAIR/miR-17-5p/FUT2 axis contributed to OA progression via wnt/β-catenin pathway, which might provide novel insights into the function of lncRNA-driven in OA.

Indexed as

Disease ProgressionSignal TransductionAdultAgedApoptosisBase Sequencebeta CateninCartilage, ArticularCell ProliferationChondrocytesExtracellular MatrixFucosyltransferasesGalactoside 2-alpha-L-fucosyltransferaseGene Expression RegulationHumansInterleukin-1betabeta CateninFucosyltransferasesGalactoside 2-alpha-L-fucosyltransferaseHOTAIR long untranslated RNA, humanInterleukin-1betaMicroRNAsMIRN17 microRNA, humanRNA, Long Noncoding

Identifiers

PMID29907764
PMCPMC6003907
OpenAlexW2808599090

What OpenQuestion holds

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Read underepoch 390

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.