Evidence map›Paper›PMID 32986864›Full record

ReviewHepatology (Baltimore, Md.)2021

Osteopontin Takes Center Stage in Chronic Liver Disease.

Zhuolun Song, Wei Chen, Dipti Athavale, Xiaodong Ge, Romain Desert, Sukanta Das, Hui Han, Natalia Nieto

Open access · greenAbstract readReview
In one paragraph

Review in Hepatology (Baltimore, Md.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 1 pooled it
18.6field-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

131 citing papers in PubMed, 1 synthesis or guideline pooled it, 215 citations in OpenAlex.

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  20. VCAM-1 and Osteopontin Link Hemodynamic Alteration to Fibrosis in Portal Hypertension.Cellular and molecular gastroenterology and hepatology · 2026
    Article

71 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 1 institution in 1 country.

Zhuolun SongDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.ORCID 0000-0001-5101-3950
Wei ChenDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.
Dipti AthavaleDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.
Xiaodong GeDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.
Romain DesertDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.
Sukanta DasDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.
Hui HanDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.
Natalia NietoDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.ORCID 0000-0002-7941-6804
University of Illinois Chicago · US

Funding

Pathogenic role of hepatocyte-derived high-mobility group box-1 isoforms as potential therapeutic targets to prevent and/or resolve liver fibrosisR01DK111677 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI NIETO, NATALIA · 2017 to 2020
$2.0M
High-mobility group box-1 and alcoholic liver diseaseR01AA025907 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI NIETO, NATALIA · 2018 to 2022
$1.8M
Pathogenic role of a protein complex of liver origin as regulator of a proinflammatory program that drives hepatic and intestinal injury in alcoholic liver diseaseI01BX005093 · VA · JESSE BROWN VA MEDICAL CENTER · PI NIETO, NATALIA · 2021 to 2025
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BLRD VA I01 BX005093NIAAA NIH HHS R01 AA025907NIDDK NIH HHS R01 DK111677
6 · The paper itself

Abstract

Osteopontin (OPN) was first identified in 1986. The prefix osteo- means bone; however, OPN is expressed in other tissues, including liver. The suffix -pontin means bridge and denotes the role of OPN as a link protein within the extracellular matrix. While OPN has well-established physiological roles, multiple "omics" analyses suggest that it is also involved in chronic liver disease. In this review, we provide a summary of the OPN gene and protein structure and regulation. We outline the current knowledge on how OPN is involved in hepatic steatosis in the context of alcoholic liver disease and non-alcoholic fatty liver disease. We describe the mechanisms whereby OPN participates in inflammation and liver fibrosis and discuss current research on its role in hepatocellular carcinoma and cholangiopathies. To conclude, we highlight important points to consider when doing research on OPN and provide direction for making progress on how OPN contributes to chronic liver disease.

Indexed as

AnimalsCarcinoma, HepatocellularDisease Models, AnimalExtracellular MatrixGene ExpressionHumansLiver CirrhosisLiver Diseases, AlcoholicLiver NeoplasmsMiceNon-alcoholic Fatty Liver DiseaseOsteopontinOsteopontinSPP1 protein, human

Identifiers

PMID32986864
PMCPMC8106357
OpenAlexW3088941414

What OpenQuestion holds

Textmetadata
LicenceTDM
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.