Evidence map›Paper›PMID 34638423›Full record

ArticleCancers2021

Maraviroc Prevents HCC Development by Suppressing Macrophages and the Liver Progenitor Cell Response in a Murine Chronic Liver Disease Model.

Adam M Passman, Robyn P Strauss, Sarah B McSpadden, Megan Finch-Edmondson, Neil Andrewartha, Ken H Woo, Luke A Diepeveen, Weihao Zhao, Joaquín Fernández-Irigoyen, Enrique Santamaría and 14 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  7. Targeting cytokine and chemokine signaling pathways for cancer therapy.Signal transduction and targeted therapy · 2024
    Review
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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

24 authors at 8 institutions in 4 countries.

Adam M PassmanSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0000-0003-3212-6938
Robyn P StraussSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Sarah B McSpaddenSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Megan Finch-EdmondsonSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0000-0002-9628-5842
Neil AndrewarthaSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Ken H WooSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Luke A DiepeveenSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Weihao ZhaoSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Joaquín Fernández-IrigoyenProteored-ISCIII, Proteomics Platform, Navarrabiomed, Navarra Health Department, Navarra Institute for Health Research (IdiSNA), Public University of Navarra, 31008 Pamplona, Spain.
Enrique SantamaríaProteored-ISCIII, Proteomics Platform, Navarrabiomed, Navarra Health Department, Navarra Institute for Health Research (IdiSNA), Public University of Navarra, 31008 Pamplona, Spain.ORCID 0000-0001-8046-8102
Laura Medina-RuizInstitute of Infection, Immunity and Inflammation, Glasgow Biomedical Research Center, University of Glasgow, Glasgow G12 8TA, UK.
Martyna SzpakowskaImmuno-Pharmacology and Interactomics Department of Infection and Immunity, Luxembourg Institute of Health, 4354 Esch-sur-Alzette, Luxembourg.ORCID 0000-0002-5659-8377
Andy ChevignéImmuno-Pharmacology and Interactomics Department of Infection and Immunity, Luxembourg Institute of Health, 4354 Esch-sur-Alzette, Luxembourg.ORCID 0000-0003-4768-6743
Hyerin ParkCentre for Medical Research, Harry Perkins Institute of Medical Research, Nedlands, WA 6009, Australia.
Rodrigo CarlessiCurtin Medical School, Curtin Health Innovation Research Institute, Curtin University, Bentley, WA 6102, Australia.ORCID 0000-0003-0038-7391
Janina E E Tirnitz-ParkerCurtin Medical School, Curtin Health Innovation Research Institute, Curtin University, Bentley, WA 6102, Australia.
José R BlancoInfectious Diseases Area, Hospital San Pedro-Center for Biomedical Research of La Rioja, 26006 Logroño, Spain.ORCID 0000-0002-4268-0150
Roslyn LondonSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Bernard A CallusSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Caryn L ElsegoodSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Murray V BakerSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Alfredo MartínezOncology Area, Center for Biomedical Research of La Rioja, 26006 Logroño, Spain.ORCID 0000-0003-4882-4044
George C T YeohSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Laura Ochoa-CallejeroOncology Area, Center for Biomedical Research of La Rioja, 26006 Logroño, Spain.ORCID 0000-0001-5366-6613
The University of Western Australia · AUCenter for Biomedical Research of La Rioja · ESCurtin University · AULuxembourg Institute of Health · LUNavarrabiomed · ESHospital San Pedro · ESMurdoch University · AUUniversity of Glasgow · GB

Funding

F.R.S.-FNRS-Télévie 7.4529.19F.R.S.-FNRS-Télévie 7.4593.19F.R.S.-FNRS-Télévie 7.8504.20Luxembourg National Research Fund 15/10358798The Proteomics Platform of Navarrabiomed (PRB3-ISCIII) PT17/0019/009
6 · The paper itself

Abstract

Maraviroc (MVC), a CCR5 antagonist, reduces liver fibrosis, injury and tumour burden in mice fed a hepatocarcinogenic diet, suggesting it has potential as a cancer therapeutic. We investigated the effect of MVC on liver progenitor cells (LPCs) and macrophages as both have a role in hepatocarcinogenesis. Mice were fed the hepatocarcinogenic choline-deficient, ethionine-supplemented diet (CDE) ± MVC, and immunohistochemistry, RNA and protein expression were used to determine LPC and macrophage abundance, migration and related molecular mechanisms. MVC reduced LPC numbers in CDE mice by 54%, with a smaller reduction seen in macrophages. Transcript and protein abundance of LPC-associated markers correlated with this reduction. The CDE diet activated phosphorylation of AKT and STAT3 and was inhibited by MVC. LPCs did not express

Indexed as

CCL5 chemokinehepatocellular carcinomaliver progenitor cellsmacrophagesMaraviroc

Identifiers

PMID34638423
PMCPMC8508380
OpenAlexW3203929897

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.