Evidence map›Paper›PMID 32265939›Full record

ReviewFrontiers in immunology2020

Versican-A Critical Extracellular Matrix Regulator of Immunity and Inflammation.

Thomas N Wight, Inkyung Kang, Stephen P Evanko, Ingrid A Harten, Mary Y Chang, Oliver M T Pearce, Carys E Allen, Charles W Frevert

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 177 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed, 1 pooled it
13.7field-weighted citation impact, top 1% 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

177 citing papers in PubMed, 1 synthesis or guideline pooled it, 256 citations in OpenAlex.

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117 more citing papers are in PubMed but not listed here.

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 2 countries.

Thomas N WightMatrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, United States.
Inkyung KangMatrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, United States.
Stephen P EvankoMatrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, United States.
Ingrid A HartenMatrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, United States.
Mary Y ChangDivision of Pulmonary/Critical Care Medicine, Center for Lung Biology, University of Washington School of Medicine, Seattle, WA, United States.
Oliver M T PearceCentre for the Tumour Microenvironment, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Carys E AllenCentre for the Tumour Microenvironment, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Charles W FrevertDivision of Pulmonary/Critical Care Medicine, Center for Lung Biology, University of Washington School of Medicine, Seattle, WA, United States.
Benaroya Research InstituteQueen Mary University of London · GBUniversity of Washington · US

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Karin E Bornfeldt · 1986 to 2026
$41.4M
Regulation of the Innate Immune Response by the Epithelium in AsthmaU19AI125378 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI ZIEGLER, STEVEN F · 2016 to 2020
$9.2M
Regulation of Allergen-Induced Airway Pathophysiology by VersicanR01AI130280 · NIAID · UNIVERSITY OF WASHINGTON · PI FREVERT, CHARLES WAYNE, HALLSTRAND, TEAL S · 2019 to 2023
$3.8M
Lymph Node Extracellular Matrix in Antigen Presentation and Immune RegulationR01DK096087 · NIDDK · STANFORD UNIVERSITY · PI BOLLYKY, PAUL L · 2012 to 2021
$3.4M
Impact of versican deficiency on the innate immune response to influenza virusR01AI136468 · NIAID · UNIVERSITY OF WASHINGTON · PI ALTEMEIER, WILLIAM A, FREVERT, CHARLES WAYNE · 2018 to 2022
$3.1M
Cancer Research UK 27947Cancer Research UK A27947NIAID NIH HHS R01 AI130280NIAID NIH HHS R01 AI136468NIAID NIH HHS U19 AI125378NIDDK NIH HHS P30 DK017047NIDDK NIH HHS R01 DK096087
6 · The paper itself

Abstract

The extracellular matrix (ECM) proteoglycan, versican increases along with other ECM versican binding molecules such as hyaluronan, tumor necrosis factor stimulated gene-6 (TSG-6), and inter alpha trypsin inhibitor (IαI) during inflammation in a number of different diseases such as cardiovascular and lung disease, autoimmune diseases, and several different cancers. These interactions form stable scaffolds which can act as "landing strips" for inflammatory cells as they invade tissue from the circulation. The increase in versican is often coincident with the invasion of leukocytes early in the inflammatory process. Versican interacts with inflammatory cells either indirectly via hyaluronan or directly via receptors such as CD44, P-selectin glycoprotein ligand-1 (PSGL-1), and toll-like receptors (TLRs) present on the surface of immune and non-immune cells. These interactions activate signaling pathways that promote the synthesis and secretion of inflammatory cytokines such as TNFα, IL-6, and NFκB. Versican also influences inflammation by interacting with a variety of growth factors and cytokines involved in regulating inflammation thereby influencing their bioavailability and bioactivity. Versican is produced by multiple cell types involved in the inflammatory process. Conditional total knockout of versican in a mouse model of lung inflammation demonstrated significant reduction in leukocyte invasion into the lung and reduced inflammatory cytokine expression. While versican produced by stromal cells tends to be pro-inflammatory, versican expressed by myeloid cells can create anti-inflammatory and immunosuppressive microenvironments. Inflammation in the tumor microenvironment often contains elevated levels of versican. Perturbing the accumulation of versican in tumors can inhibit inflammation and tumor progression in some cancers. Thus versican, as a component of the ECM impacts immunity and inflammation through regulating immune cell trafficking and activation. Versican is emerging as a potential target in the control of inflammation in a number of different diseases.

Indexed as

AnimalsExtracellular MatrixHumansHyaluronic AcidInflammationLeukocytesLipopolysaccharidesLymphocyte SubsetsMiceModels, AnimalMyeloid CellsRabbitsRatsReceptors, Cell SurfaceStromal CellsToll-Like ReceptorsHyaluronic AcidLipopolysaccharidesReceptors, Cell SurfaceToll-Like ReceptorsVCAN protein, humanVcan protein, mouseVersicanshyaluronanimmunityinflammationmacrophagesT lymphocytesversican

Identifiers

PMID32265939
PMCPMC7105702
OpenAlexW3013536489

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.