Evidence map›Paper›PMID 34539990›Full record

ArticleAmerican journal of translational research2021

miR-590-5p affects chondrocyte proliferation, apoptosis, and inflammation by targeting FGF18 in osteoarthritis.

Peng Jiang, Xixi Dou, Shuaiguang Li, Qingwen Jia, Peixue Ling, Hongyu Liu, Qiuju Han, Shui Sun

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Analysis of miRNAs inPharmaceuticals (Basel, Switzerland) · 2023
    Article
  5. Article
  6. Article
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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

8 authors at 3 institutions in 1 country.

Peng JiangDepartment of Orthopaedics, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University Jinan, Shandong Province, China.
Xixi DouShandong Provincial Key Laboratory of Transmucosal and Transdermal Drug Delivery, Shandong Freda Pharmaceutical Group Co., Ltd. Jinan, Shandong Province, China.
Shuaiguang LiDepartment of Pharmacy, Cheeloo College of Medicine, Shandong University Jinan, Shandong, China.
Qingwen JiaShandong Provincial Key Laboratory of Transmucosal and Transdermal Drug Delivery, Shandong Freda Pharmaceutical Group Co., Ltd. Jinan, Shandong Province, China.
Peixue LingShandong Provincial Key Laboratory of Transmucosal and Transdermal Drug Delivery, Shandong Freda Pharmaceutical Group Co., Ltd. Jinan, Shandong Province, China.
Hongyu LiuProsit Sole Biotechnology A302, No. 5 Kaituo Road, Haidian District, Beijing, China.
Qiuju HanInstitute of Immunopharmaceutical Sciences, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University Jinan 250012, Shandong, China.
Shui SunDepartment of Orthopaedics, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University Jinan, Shandong Province, China.
Shandong University · CNShandong Academy of Pharmaceutical Sciences · CNBeijing VDJBio (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the potential miRNA targeting FGF18, and its role in regulating the proliferation, apoptosis and inflammation in human primary chondrocytes.

methodsThe normal human chondrocytes were induced by IL-1β to mimic OA

resultsTarget Scan analysis predicted that FGF18 is directly targeted by miR-590-5p. miR-590-5p was up-regulated, whereas FGF18 expression was inhibited in IL-1β-induced chondrocytes. miR-590-5p mimics reduced the expression of FGF18 protein, inhibited the cell viability of chondrocytes, and promoted secretion of inflammatory factors in chondrocytes, while miR-590-5p inhibitors increased FGF18 levels in IL-1β-treated chondrocytes. Furthermore, expression of inflammatory factors in chondrocytes was reduced by miR-590-5p inhibitors. The luciferase reporter assay showed that miR-590-5p could target FGF18.

conclusionsmiR-590-5p promotes OA progression by targeting FGF18, which serves as a potential therapeutic target for OA.

Indexed as

ChondrocytesFGF18miR-590-5posteoarthritis

Identifiers

PMID34539990
PMCPMC8430182
OpenAlexW3200650197

What OpenQuestion holds

Textmetadata
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.