Evidence map›Paper›PMID 29038477›Full record

ArticleScientific reports2017

Long non-coding HCG18 promotes intervertebral disc degeneration by sponging miR-146a-5p and regulating TRAF6 expression.

Yanhai Xi, Tingwang Jiang, Weiheng Wang, Jiangming Yu, Yang Wang, Xueming Wu, Yunfei He

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
6.7field-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

73 citing papers in PubMed, 123 citations in OpenAlex.

  1. Review
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  14. The role of long non-coding RNA HCG18 in cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  15. Mechanobiology of MicroRNAs in Intervertebral Disk Degeneration.Journal of spine research and surgery · 2023
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

13 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

7 authors at 2 institutions in 1 country.

Yanhai XiDepartment of Spine Surgery, Changzheng hospital, Second Military Medical University, Shanghai, 200003, China. xiyanhai1778@qq.com.
Tingwang JiangDepartment of Immunology and Microbiology, Institution of Laboratory Medicine of Changshu, Changshu, 215500, Jiangsu, China.
Weiheng WangDepartment of Spine Surgery, Changzheng hospital, Second Military Medical University, Shanghai, 200003, China.
Jiangming YuDepartment of Spine Surgery, Changzheng hospital, Second Military Medical University, Shanghai, 200003, China.
Yang WangDepartment of Spine Surgery, Changzheng hospital, Second Military Medical University, Shanghai, 200003, China.
Xueming WuDepartment of Spine Surgery, Changzheng hospital, Second Military Medical University, Shanghai, 200003, China.
Yunfei HeDepartment of Spine Surgery, Changzheng hospital, Second Military Medical University, Shanghai, 200003, China.
Second Military Medical University · CNChangshu No.1 People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intervertebral disc degeneration (IDD) is associated with the deterioration of nucleus pulposus (NP) cells due to hypertrophic differentiation and calcification. Emerging studies have shown that long noncoding RNAs (lncRNAs) play critical roles in the development of IDD. Using bioinformatics prediction, we hereby sought to identify the lncRNAs that regulate the expression of microRNA-146a-5p (miR-146a-5p), an IDD-related inflammatory factor. Our study demonstrated that lncRNA HCG18 acted as an endogenous sponge to down-regulate miR-146a-5p expression in the NP cells by directly binding to miR-146a-5p. In addition, HCG18 expression was up-regulated in the patients with IDD, bulging or herniated discs, and its level was positively correlated with the disc degeneration grade. In vitro, miR-146a-5p up-regulation HCG18 retarded the growth of NP cells by decreasing S phase of cell cycle, inducing cell apoptosis, recruitment of macrophages and hypercalcification. Conversely, down-regulation of miR-146a-5p exerted opposite effects. Furthermore, we elucidated that TRAF6, a target gene by miR-146a-5p, was modulated by HCG18 expression. Restore of TRAF6 expression by virus infection reserved the effect of HCG18 on the NP cells. Altogether, our data indicated that HCG18 suppressed the growth of NP cells and promoted the IDD development via the miR-146a-5p/TRAF6/NFκB axis.

Indexed as

ApoptosisDown-RegulationHumansIntervertebral Disc DegenerationMacrophagesMicroRNAsNucleus PulposusOsteogenesisRNA, Long NoncodingTNF Receptor-Associated Factor 6MicroRNAsMIRN146 microRNA, humanRNA, Long NoncodingTNF Receptor-Associated Factor 6

Identifiers

PMID29038477
PMCPMC5643303
OpenAlexW2763440116

What OpenQuestion holds

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LicenceCC BY
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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.