Evidence map›Paper›PMID 32732957›Full record

ArticleCell death & disease2020

LEF1 mediates osteoarthritis progression through circRNF121/miR-665/MYD88 axis via NF-кB signaling pathway.

Tianfu Wang, Zhiyu Hao, Changcheng Liu, Lebin Yuan, Li Li, Menghong Yin, Qing Li, Zhiming Qi, Zi Wang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. 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 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  7. Role of non‑coding RNAs in cartilage endplate (Review).Experimental and therapeutic medicine · 2023
    Review
  8. Review
  9. Circular RNAs: typical biomarkers for bone-related diseases.Journal of Zhejiang University. Science. B · 2022
    Article
  10. Review
  11. Lef1 ablation alleviates cartilage mineralization following posttraumatic osteoarthritis induction.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Review
  13. Review
  14. Article
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Tianfu WangDepartment of Sports Medicine, Dalian Municipal Central Hospital, Dalian, 116033, Liaoning Province, China.
Zhiyu HaoDepartment of Medical Imageology, Dalian Medical University, Dalian, 116044, Liaoning Province, China.
Changcheng LiuDepartment of Sports Medicine, Dalian Municipal Central Hospital, Dalian, 116033, Liaoning Province, China.
Lebin YuanDepartment of Sports Medicine, Dalian Municipal Central Hospital, Dalian, 116033, Liaoning Province, China.
Li LiDepartment of Sports Medicine, Dalian Municipal Central Hospital, Dalian, 116033, Liaoning Province, China.
Menghong YinDepartment of Sports Medicine, Dalian Municipal Central Hospital, Dalian, 116033, Liaoning Province, China.
Qing LiDepartment of Sports Medicine, Dalian Municipal Central Hospital, Dalian, 116033, Liaoning Province, China.
Zhiming QiDepartment of Sports Medicine, Dalian Municipal Central Hospital, Dalian, 116033, Liaoning Province, China.
Zi WangDepartment of Sports Medicine, Dalian Municipal Central Hospital, Dalian, 116033, Liaoning Province, China. dlwangzi0815@163.com.
Dalian Municipal Central Hospital · CNDalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is a joint disease that causes great pain to patients and imposes a tremendous burden on the world's medical resources. Regulatory noncoding RNAs, including circular RNAs (circRNAs) and microRNAs (miRNAs), play an important role in OA progression. Here, we identified differential expression of transcription factor LEF1 that increased circRNA circRNF121 levels in normal and OA cartilage tissues. The expression of LEF1 and circRNF121 was positively associated with Mankin's scores. Alteration of circRNF121 mediated the degradation of extracellular mechanisms (ECM), apoptosis, and proliferation of chondrocytes. MiR-665 was identified as a direct regulatory target of circRNF121 and MYD88. Functional analysis showed that circRNF121 and MYD88 modulated ECM degradation, apoptosis, and proliferation of chondrocytes, which could be reversed by miR-665. MYD88 regulated the activity of the NF-кB signaling pathway by circRNF121 via sponging miR-665. Collectively, these data indicated that LEF1 impacted OA progression by modulating the circRNF121/miR-665/MYD88 axis via NF-кB pathway. Our research proposed a new molecular mechanism for the development of OA, and provided a prospective therapeutic target for OA.

Indexed as

Disease ProgressionAdultAnimalsApoptosisCartilage, ArticularCell ProliferationChondrocytesExtracellular MatrixGene Expression ProfilingGene Expression RegulationHumansLymphoid Enhancer-Binding Factor 1MaleMicroRNAsMiddle AgedModels, BiologicalLymphoid Enhancer-Binding Factor 1MicroRNAsMIRN665 microRNA, humanMyeloid Differentiation Factor 88NF-kappa BRNA, Circular

Identifiers

PMID32732957
PMCPMC7393488
OpenAlexW3046886179

What OpenQuestion holds

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LicenceCC BY
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.