Evidence map›Paper›PMID 29393457›Full record

ArticleMolecular medicine reports2018

Intermittent cyclic mechanical tension altered the microRNA expression profile of human cartilage endplate chondrocytes.

Chencheng Feng, Minghan Liu, Xin Fan, Minghui Yang, Huan Liu, Yue Zhou

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Role of non‑coding RNAs in cartilage endplate (Review).Experimental and therapeutic medicine · 2023
    Review
  9. Article
  10. Role of microRNAs in intervertebral disc degeneration (Review).Experimental and therapeutic medicine · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. 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

6 authors at 2 institutions in 1 country.

Chencheng Feng *Department of Orthopedics, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, P.R. China.
Minghan Liu *Department of Orthopedics, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, P.R. China.
Xin FanDepartment of Orthopedics, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, P.R. China.
Minghui YangDepartment of Orthopedics, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, P.R. China.
Huan LiuDepartment of Orthopedics, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, P.R. China.
Yue ZhouDepartment of Orthopedics, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, P.R. China.
Army Medical University · CNXinqiao Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies have identified the association between cartilage endplate (CEP) degeneration and abnormal mechanical loading. Several studies have reported that intermittent cyclic mechanical tension (ICMT) regulates CEP degeneration via various biological processes and signaling pathways. However, the functions of microRNAs in regulating the cellular responses of CEP chondrocytes to ICMT remain to be elucidated. The current study determined the differentially expressed microRNAs in human CEP chondrocytes exposed to ICMT using microarray analysis. A total 21 significantly upregulated and 62 downregulated miRNAs were identified compared with the control. The findings were subsequently partially validated by reverse transcription‑quantitative polymerase chain reaction. Potential target genes of the significantly differentially expressed miRNAs were predicted using bioinformatics analysis and were used for Gene Ontology analysis and Kyoto Encyclopedia of Genes and Genomes pathway analysis. The present study revealed that the significantly differentially expressed microRNAs were involved in various signaling pathways and biological processes that are crucial to regulating the responses of CEP chondrocytes to ICMT. The current study provided a global view of microRNA expression in CEP chondrocytes under mechanical stimulation, suggesting that microRNAs are important for regulating the mechanical response of CEP chondrocytes. Additionally, it provided a novel insight into the association between mechanical stress and the establishment and progression of intervertebral disc degeneration.

Indexed as

Gene ExpressionMechanical PhenomenaTranscriptomeAdultCartilageCells, CulturedChondrocytesComputational BiologyFemaleGene Expression ProfilingGene OntologyHumansIntervertebral DiscMaleMicroRNAsMiddle AgedMicroRNAscartilage endplate calcificationcartilage endplate chondrocytescyclic mechanical tensionintervertebral disc degenerationmicroRNA

Identifiers

PMID29393457
PMCPMC5865992
OpenAlexW2787383387

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.