Evidence map›Paper›PMID 32685902›Full record

ArticleResearch and practice in thrombosis and haemostasis2020

Liver fibrosis is driven by protease-activated receptor-1 expressed by hepatic stellate cells in experimental chronic liver injury.

Lauren G Poole, Asmita Pant, Holly M Cline-Fedewa, Kurt J Williams, Bryan L Copple, Joseph S Palumbo, James P Luyendyk

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 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
1.3field-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

10 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

7 authors at 2 institutions in 1 country.

Lauren G PooleInstitute for Integrative Toxicology Michigan State University East Lansing MI USA.
Asmita PantDepartment of Pathobiology & Diagnostic Investigation Michigan State University East Lansing MI USA.ORCID https://orcid.org/0000-0003-4468-8639
Holly M Cline-FedewaDepartment of Pathobiology & Diagnostic Investigation Michigan State University East Lansing MI USA.
Kurt J WilliamsDepartment of Pathobiology & Diagnostic Investigation Michigan State University East Lansing MI USA.
Bryan L CoppleDepartment of Pharmacology and Toxicology Michigan State University East Lansing MI USA.
Joseph S PalumboCancer and Blood Diseases Institute Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine Cincinnati OH USA.
James P LuyendykInstitute for Integrative Toxicology Michigan State University East Lansing MI USA.
Michigan State University · USCincinnati Children's Hospital Medical Center · US

Funding

MULTIDISCIPLINARY TRAINING IN ENVIRONMENTAL TOXICOLOGYT32ES007255 · NIEHS · MICHIGAN STATE UNIVERSITY · PI JOHN J LAPRES · 1989 to 2026
$9.3M
Novel anti-fibrotic mechanisms in chemical-induced liver injuryR01ES017537 · NIEHS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI LUYENDYK, JAMES P · 2009 to 2019
$3.6M
Hemostatic Factors Drive Prostate Cancer PathogenesisR01CA193678 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI PALUMBO, JOSEPH S. · 2016 to 2020
$1.8M
Coagulation factors as modifiers of the colon cancer microenvironmentR01CA204058 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI PALUMBO, JOSEPH S. · 2016 to 2020
$1.8M
RISK MANAGEMENT IN NATIVE AMERICAN COMMUNITIESR25ES007255 · NIEHS · CLARK UNIVERSITY (WORCESTER, MA) · PI GOBLE, ROBERT L · 1994 to 2002
$738k
Mechanisms of fibrin(ogen)-directed macrophage activation in liver toxicityF32DK121423 · NIDDK · MICHIGAN STATE UNIVERSITY · PI POOLE, LAUREN G · 2019 to 2019
$62k
NCI NIH HHS R01 CA193678NCI NIH HHS R01 CA204058NIDDK NIH HHS F32 DK121423NIEHS NIH HHS R01 ES017537NIEHS NIH HHS R25 ES007255NIEHS NIH HHS T32 ES007255
6 · The paper itself

Abstract

backgroundBlood coagulation protease activity is proposed to drive hepatic fibrosis through activation of protease-activated receptors (PARs). Whole-body PAR-1 deficiency reduces experimental hepatic fibrosis, and

methodsPAR-1

resultsPAR-1 mRNA levels were reduced (>95%) in hepatic stellate cells isolated from PAR-1

conclusionsThe results constitute the first direct experimental evidence that PAR-1 expressed by stellate cells directly promotes their profibrogenic phenotype and hepatic fibrosis

Indexed as

carbon tetrachloridecollagenhepatic stellate cellsliver fibrosisPAR‐1receptorthrombin

Identifiers

PMID32685902
PMCPMC7354391
OpenAlexW3037496798

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.