Evidence map›Paper›PMID 29434766›Full record

ArticleExperimental and therapeutic medicine2018

MicroRNA-17-5p contributes to osteoarthritis progression by binding p62/SQSTM1.

Huihui Li, Daoyi Miao, Qi Zhu, Jianghua Huang, Guangxian Lu, Weiguo Xu

RetractedOpen access · diamondAbstract readRetracted Publication
In one paragraph

Article in Experimental and therapeutic medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

  1. Programmed cell death in osteoarthritis.Apoptosis : an international journal on programmed cell death · 2026
    Review
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  18. Non-Coding RNAs in Cartilage Development: An Updated Review.International journal of molecular sciences · 2019
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Huihui LiDepartment of Orthopedics and Traumatology, Ruian City People's Hospital of Chinese Medicine, Ruian, Zhejiang 325200, P.R. China.
Daoyi MiaoDepartment of Hand Surgery, Ruian Municipal People's Hospital, Ruian, Zhejiang 325200, P.R. China.
Qi ZhuDepartment of Hand Surgery, Ruian Municipal People's Hospital, Ruian, Zhejiang 325200, P.R. China.
Jianghua HuangDepartment of Orthopedics and Traumatology, Ruian City People's Hospital of Chinese Medicine, Ruian, Zhejiang 325200, P.R. China.
Guangxian LuDepartment of Orthopedics and Traumatology, Ruian City People's Hospital of Chinese Medicine, Ruian, Zhejiang 325200, P.R. China.
Weiguo XuDepartment of Orthopedics and Traumatology, Ruian City People's Hospital of Chinese Medicine, Ruian, Zhejiang 325200, P.R. China.
Wenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy has been reported to be widely involved in the pathogenesis of osteoarthritis (OA). Increasing evidence suggested the important role of microRNAs (miRs) in the progression of OA. However, the functional role of miR-17-5p in OA development has remained to be fully elucidated. First, a mouse model of OA was established and the relative level of miR-17-5p was determined using PCR. Safranin O-fast green staining was applied to determine cartilage degeneration. TargetScan software and a dual luciferase reporter assay were applied to determine potential target genes of miR-17-5P. Autophagy measurement was performed using green fluorescent protein-microtubule-associated protein 1 light chain 3 (LC3) dot analysis. The results demonstrated that the relative expression of miR-17-5p was significantly decreased in OA model mice. In addition, the level of miR-17-5p was decreased in SW1353 human chondrosarcoma cells treated with interleukin-1β. Furthermore, autophagy was found to be suppressed in the knee joints of experimental OA model mice. The dual luciferase reporter assay confirmed that p62/sequestosome 1 was a target gene of miR-17-5p. Of note, miR-17-5p inhibitor-induced reduction of LC3 dots was markedly reversed by knockdown of p62 in SW1353 cells. In conclusion, decreased miR-17-5p expression in chondrocytes induced autophagy mainly through suppressing the expression of p62, thereby contributing to OA progression.

Indexed as

autophagymiR-17-5posteoarthritisp62/SQSTM1

Identifiers

PMID29434766
PMCPMC5776526
OpenAlexW2775615006

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.