Evidence map›Paper›PMID 35159339›Full record

ArticleCells2022

Induction of Pro-Fibrotic CLIC4 in Dermal Fibroblasts by TGF-β/Wnt3a Is Mediated by GLI2 Upregulation.

Christopher W Wasson, Begoña Caballero-Ruiz, Justin Gillespie, Emma Derrett-Smith, Jamel Mankouri, Christopher P Denton, Gianluca Canettieri, Natalia A Riobo-Del Galdo, Francesco Del Galdo

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 13 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

9 authors at 3 institutions in 2 countries.

Christopher W WassonLeeds Institute of Rheumatic and Musculoskeletal Medicine, Faculty of Medicine and Health, University of Leeds, Leeds LS29JT, UK.
Begoña Caballero-RuizSchool of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS29JT, UK.
Justin GillespieLeeds Institute of Rheumatic and Musculoskeletal Medicine, Faculty of Medicine and Health, University of Leeds, Leeds LS29JT, UK.
Emma Derrett-SmithCentre for Rheumatology and Connective Tissue Diseases, UCL Division of Medicine, London NW32PF, UK.
Jamel MankouriSchool of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS29JT, UK.
Christopher P DentonCentre for Rheumatology and Connective Tissue Diseases, UCL Division of Medicine, London NW32PF, UK.
Gianluca CanettieriDepartment of Molecular Medicine, Sapienza University of Rome, 00196 Rome, Italy.ORCID 0000-0001-6694-2613
Natalia A Riobo-Del GaldoSchool of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS29JT, UK.ORCID 0000-0002-8942-7873
Francesco Del GaldoLeeds Institute of Rheumatic and Musculoskeletal Medicine, Faculty of Medicine and Health, University of Leeds, Leeds LS29JT, UK.ORCID 0000-0002-8528-2283
University of Leeds · GBUniversity College London · GBSapienza University of Rome · IT

Funding

Biotechnology and Biological Sciences Research Council BB/S01716X/1
6 · The paper itself

Abstract

Chloride intracellular channel 4 (CLIC4) is a recently discovered driver of fibroblast activation in Scleroderma (SSc) and cancer-associated fibroblasts (CAF). CLIC4 expression and activity are regulated by TGF-β signalling through the SMAD3 transcription factor. In view of the aberrant activation of canonical Wnt-3a and Hedgehog (Hh) signalling in fibrosis, we investigated their role in CLIC4 upregulation. Here, we show that TGF-β/SMAD3 co-operates with Wnt3a/β-catenin and Smoothened/GLI signalling to drive CLIC4 expression in normal dermal fibroblasts, and that the inhibition of β-catenin and GLI expression or activity abolishes TGF-β/SMAD3-dependent CLIC4 induction. We further show that the expression of the pro-fibrotic marker α-smooth muscle actin strongly correlates with CLIC4 expression in dermal fibroblasts. Further investigations revealed that the inhibition of CLIC4 reverses morphogen-dependent fibroblast activation. Our data highlights that CLIC4 is a common downstream target of TGF-β, Hh, and Wnt-3a through signalling crosstalk and we propose a potential therapeutic avenue using CLIC4 inhibitors.

Indexed as

beta CateninChloride ChannelsTransforming Growth Factor betaWnt3A ProteinZinc Finger Protein Gli2FibroblastsFibrosisHedgehog ProteinsHumansNuclear ProteinsUp-Regulationbeta CateninChloride ChannelsCLIC4 protein, humanGLI2 protein, humanHedgehog ProteinsNuclear ProteinsTransforming Growth Factor betaWnt3A ProteinWNT3A protein, humanZinc Finger Protein Gli2CLIC4fibrosisIon channelsmorphogensScleroderma

Identifiers

PMID35159339
PMCPMC8834396
OpenAlexW4210799849

What OpenQuestion holds

Textmetadata
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.