Evidence map›Paper›PMID 35791460›Full record

ArticleCell proliferation2022

CircNFIX regulates chondrogenesis and cartilage homeostasis by targeting the miR758-3p/KDM6A axis.

Hongyi Liao, Qingqiang Tu, Yunze Kang, Guping Mao, Zhiwen Li, Shu Hu, Puyi Sheng, Xudong Wang, Yiyang Xu, Dianbo Long and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2022. 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
1.3field-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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

13 authors at 1 institution in 1 country.

Hongyi LiaoDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Qingqiang TuDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yunze KangDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Guping MaoDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Zhiwen LiDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Shu HuDepartment of Joint Surgery, Center for Orthopaedic Surgery, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China.
Puyi ShengDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xudong WangDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yiyang XuDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Dianbo LongDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yuanyuan XuDepartment of Pediatric Nephrology and Rheumatology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yan KangDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Ziji ZhangDepartment of Joint Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.ORCID https://orcid.org/0000-0002-7040-8576
Sun Yat-sen University · CN

Funding

National Natural Science Foundation of China 81874014The Natural Science Foundation of Guangdong Province, China 2022A1515012279
6 · The paper itself

Abstract

objectivesOsteoarthritis (OA) is a degenerative disease causing the progressive destruction of articular cartilage; however, the aetiology has not yet been elucidated. Circular RNAs (circRNAs) are reportedly involved in cartilage degeneration and OA development. In the present study, we identified that circNFIX regulates chondrogenesis and cartilage homeostasis. MATERIALS AND

methodsMicroarray analysis was performed to explore circRNA expression during the chondrogenic differentiation of human adipose-drived stem cells (hADSCs). CircNFIX expression was determined using quantitative reverse transcription-polymerase chain reaction and in situ hybridization. Gain- and loss-of-function assays were performed to validate the role of circNFIX in cartilage homeostasis. RNA pull-down, Argonaute2-RNA immunoprecipitation and luciferase reporter assays were performed to evaluate the interactions among circNFIX, miR758-3p and KDM6A.

resultsCircNFIX expression was upregulated in the early and middle stages, whereas downregulated in the late stage of hADSC chondrogenesis. CircNFIX inhibition attenuated hADSC chondrogenesis. CircNFIX was remarkably downregulated in OA samples, circNFIX overexpression protected against chondrocyte degradation and alleviated OA progression in the destabilization of the medial meniscus OA model. Mechanistically, circNFIX acted as a sponge of miR758-3p and played a role in the chondrogenesis and chondrocyte degeneration by targeting the miR-758-3p/KDM6A axis.

conclusionsOur results revealed a key role of circNFIX in chondrogenesis and cartilage homeostasis, which may provide a potential therapeutic strategy for OA treatment.

Indexed as

Cartilage, ArticularMicroRNAsOsteoarthritisRNA, CircularChondrocytesChondrogenesisHistone DemethylasesHomeostasisHumansNFI Transcription FactorsHistone DemethylasesKDM6A protein, humanMicroRNAsMIRN758 microRNA, humanNFI Transcription FactorsNFIX protein, humanRNA, Circular

Identifiers

PMID35791460
PMCPMC9628241
OpenAlexW4283832098

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.