Evidence map›Paper›PMID 31804973›Full record

ArticleAging2019

Long noncoding RNA LINC00958 accelerates the proliferation and matrix degradation of the nucleus pulposus by regulating miR-203/SMAD3.

Kunchi Zhao, Yang Zhang, Hongping Yuan, Mingming Zhao, Dongxu Zhao

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. CTBP1-AS2 promoted non-small cell lung cancer progression via sponging the miR-623/MMP3 axis.Environmental science and pollution research international · 2022
    Article
  5. Article
  6. Circ_0005918 Sponges miR-622 to Aggravate Intervertebral Disc Degeneration.Frontiers in cell and developmental biology · 2022
    Article
  7. Article
  8. An Oxidative Stress-Related Gene Pair (Frontiers in immunology · 2021
    Article
  9. Article
  10. Review
  11. Review
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

5 authors at 3 institutions in 1 country.

Kunchi ZhaoDepartment of Orthopaedic Surgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China.
Yang ZhangDepartment of Neurosurgery, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Hongping YuanDepartment of Nephrology, Jilin FAW General Hospital, Changchun, Jilin 130011, P.R. China.
Mingming ZhaoDepartment of Orthopaedic Surgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China.
Dongxu ZhaoDepartment of Orthopaedic Surgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China.
Union Hospital · CNFirst Hospital of Jilin University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence suggests that long noncoding RNAs (lncRNAs) play important roles in the development of intervertebral disc degeneration (IDD). LncRNA LINC00958 has recently been shown to play crucial roles in the development of tumors. However, the role of LINC00958 in IDD remains unclear. We showed that the expression of lncRNA LINC00958 was upregulated in degenerative NP samples, and LINC00958 expression increased gradually along with the grade of exacerbation of disc degeneration. Ectopic expression of LINC00958 promoted nucleus pulposus (NP) cell proliferation, inhibited aggrecan and Col II expression and promoted MMP-2 and MMP-13 expression. In addition, we showed that miR-203 expression was downregulated in degenerative NP samples, and miR-203 expression reduced gradually along with the grade of exacerbation of disc degeneration. Moreover, we demonstrated that the expression of miR-203 was inversely related with LINC00958 expression in NP samples. Ectopic expression of miR-203 inhibited NP cell growth and inhibited ECM degradation. Furthermore, we showed that ectopic expression of miR-203 suppressed the luciferase activity of the wild-type LINC00958 3'-UTR but not the mutant LINC00958 3'-UTR. Elevated expression of LINC00958 inhibited the expression of miR-203 and promoted the expression of SMAD3. In addition, we demonstrated that lncRNA LINC00958 exerted its function by targeting miR-203 in the NP cells. These data suggested that dysregulated lncRNA LINC00958 expression might play an important role in the development of IDD.

Indexed as

Cell ProliferationRNA, Long NoncodingAdultAggrecansAgingCollagen Type IIDown-RegulationExtracellular MatrixGene Expression RegulationHumansIntervertebral Disc DegenerationMatrix Metalloproteinase 13Matrix Metalloproteinase 2MicroRNAsMiddle AgedNucleus PulposusAggrecansCollagen Type IIMatrix Metalloproteinase 13Matrix Metalloproteinase 2MicroRNAsMIRN203 microRNA, humanMMP13 protein, humanMMP2 protein, humanRNA, Long NoncodingSmad3 ProteinSMAD3 protein, humanintervertebral disc degenerationLINC00958miR-203nucleus pulposus

Identifiers

PMID31804973
PMCPMC6932897
OpenAlexW2994472453

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.