Evidence map›Paper›PMID 32819387›Full record

ArticleJournal of orthopaedic surgery and research2020

The β-catenin/TCF-4 pathway regulates the expression of OPN in human osteoarthritic chondrocytes.

Jian Tian, Shu-Guang Gao, Yu-Sheng Li, Chao Cheng, Zhen-Han Deng, Wei Luo, Fang-Jie Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2020. 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
1.1field-weighted citation impact, top 23% 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, 14 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

7 authors at 3 institutions in 1 country.

Jian TianDepartment of Orthopaedics, Xiangya Hospital, Central South University, No.87 Xiangya Road, Changsha, 410008, Hunan, China.
Shu-Guang GaoDepartment of Orthopaedics, Xiangya Hospital, Central South University, No.87 Xiangya Road, Changsha, 410008, Hunan, China. gaoshuguang0341@qq.com.
Yu-Sheng LiDepartment of Orthopaedics, Xiangya Hospital, Central South University, No.87 Xiangya Road, Changsha, 410008, Hunan, China.
Chao ChengDepartment of Orthopaedics, Yiyang Central Hospital, Clinical Medical Technology Demonstration Base for Minimally Invasive and Digital Orthopaedics in Hunan Province, No.118 North KangFu Road, Yiyang, 413000, Hunan, China.
Zhen-Han DengDepartment of Sports Medicine, The First Hospital Affiliated to Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, 518035, Guangdong, China.
Wei LuoDepartment of Orthopaedics, Xiangya Hospital, Central South University, No.87 Xiangya Road, Changsha, 410008, Hunan, China.
Fang-Jie ZhangDepartment of Emergency Medicine, Xiangya Hospital, Central South University, No.87 Xiangya Road, Changsha, 410008, Hunan, China. zhangfj@csu.edu.cn.
Xiangya Hospital Central South University · CNCentral South University · CNShenzhen Second People's Hospital · CN

Funding

National Natrual Science Foundation of China 81672225National Natrual Science Foundation of China 81874030National Natrual Science Foundation of China 81902303National Natural Science Foundation of China 81501923the Rui E (Ruiyi) Emergency Medical Research Special Funding Project K2019007
6 · The paper itself

Abstract

backgroundCartilage destruction is the main characteristic of osteoarthritis (OA), and osteopontin (OPN) is elevated in OA articular cartilage; however, the reason for the increased OPN level is not determined. In addition, Wnt/β-catenin signaling participates in the progression of OA. The aim of the present study was to evaluate whether canonical Wnt signaling could regulate the expression of OPN in human chondrocytes in vitro.

methodsHuman chondrocytes were cultured in vitro, and we first assayed the mRNA levels of OPN and β-catenin in chondrocytes. Next, we performed transient transfection of TCF 4 shRNA into chondrocytes to inhibit TCF 4 expression and explore changes in the OPN level. Then, the Wnt/β-catenin signaling inhibitor Dickkopf-1 (Dkk-1) was incubated with chondrocytes, and we assayed the changes in β-catenin and OPN.

resultsOur results showed that the expression of both β-catenin and OPN was increased in OA chondrocytes, but there were no correlations between β-catenin and OPN expression. TCF4 shRNA downregulated the expression of TCF 4 and OPN in chondrocytes, while after treatment with rDKK-1 at a concentration of 400 ng/ml for 24 h, the mRNA and protein expression of both β-catenin and OPN was significantly decreased in chondrocytes.

conclusionsElevated OPN expression might be regulated by the β-catenin/TCF-4 pathway, and the Wnt/β-catenin inhibitor DKK1 could inhibit the expression of β-catenin and OPN in OA chondrocytes.

Indexed as

Agedbeta CateninCartilage, ArticularCells, CulturedChondrocytesDisease ProgressionFemaleGene ExpressionGene Expression RegulationHumansIntercellular Signaling Peptides and ProteinsMaleMiddle AgedMolecular Targeted TherapyOsteoarthritisOsteopontinbeta CateninDKK1 protein, humanIntercellular Signaling Peptides and ProteinsOsteopontinTranscription Factor 4ChondrocyteDickkopf 1OsteopontinTCF 4β-Catenin

Identifiers

PMID32819387
PMCPMC7441722
OpenAlexW3043349443

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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.