Evidence map›Paper›PMID 28437865›Full record

ArticleHepatology (Baltimore, Md.)2017

A novel role of astrocyte elevated gene-1 (AEG-1) in regulating nonalcoholic steatohepatitis (NASH).

Jyoti Srivastava, Chadia L Robertson, Kareem Ebeid, Mikhail Dozmorov, Devaraja Rajasekaran, Rachel Mendoza, Ayesha Siddiq, Maaged A Akiel, Nidhi Jariwala, Xue-Ning Shen and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

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  8. Oligonucleotide therapies for nonalcoholic steatohepatitis.Molecular therapy. Nucleic acids · 2024
    Review
  9. HCC-Related lncRNAs: Roles and Mechanisms.International journal of molecular sciences · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 5 institutions in 2 countries.

Jyoti SrivastavaDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Chadia L RobertsonDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Kareem EbeidDepartment of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA.
Mikhail DozmorovDepartment of Biostatistics, Virginia Commonwealth University, Richmond, VA.
Devaraja RajasekaranDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Rachel MendozaDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Ayesha SiddiqDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Maaged A AkielDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.ORCID 0000-0002-0211-2837
Nidhi JariwalaDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Xue-Ning ShenDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Jolene J WindleDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Mark A SublerDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Nitai D MukhopadhyayDepartment of Biostatistics, Virginia Commonwealth University, Richmond, VA.
Shah GiashuddinDepartment of Pathology and Laboratory Medicine, New York Methodist Hospital, Brooklyn, NY.
Shobha GhoshDepartment of Internal Medicine, Virginia Commonwealth University, Richmond, VA.
Zhao LaiGreehey Children's Cancer Research Institute, San Antonio, TX.
Yidong ChenComputational Biology and Bioinformatics, University of Texas Health Science Center San Antonio, San Antonio, TX.
Paul B FisherDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Aliasger K SalemDepartment of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA.
Arun J SanyalDepartment of Internal Medicine, Virginia Commonwealth University, Richmond, VA.
Devanand SarkarDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA.
Virginia Commonwealth University · USUniversity of Iowa · USChildren's Cancer Center · USNewYork–Presbyterian Brooklyn Methodist Hospital · USThe University of Texas Health Science Center at San Antonio · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Keri R Maher · 1985 to 2026
$51.0M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Brandi Janssen · 1990 to 2026
$40.5M
Training Grant in Digestive Diseases and Liver DiseasesT32DK007150 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI SANYAL, ARUN J · 1986 to 2017
$4.2M
The role of AEG-1 in NASH and NASH-HCCR01DK107451 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI SARKAR, DEVANAND · 2016 to 2025
$3.9M
Analysis of a novel regulator of hepatocellular carcinomaR01CA138540 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI SARKAR, DEVANAND · 2010 to 2014
$1.6M
A novel mediator of obesity associated hepatocellular carcinoma (HCC)R21CA183954 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI SARKAR, DEVANAND · 2014 to 2015
$365k
NCI NIH HHS P30 CA016059NCI NIH HHS R01 CA138540NCI NIH HHS R21 CA183954NIDDK NIH HHS R01 DK107451NIDDK NIH HHS T32 DK007150NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

Nonalcoholic steatohepatitis (NASH) is the most prevalent cause of chronic liver disease in the Western world. However, an optimum therapy for NASH is yet to be established, mandating more in-depth investigation into the molecular pathogenesis of NASH to identify novel regulatory molecules and develop targeted therapies. Here, we unravel a unique function of astrocyte elevated gene-1(AEG-1)/metadherin in NASH using a transgenic mouse with hepatocyte-specific overexpression of AEG-1 (Alb/AEG-1) and a conditional hepatocyte-specific AEG-1 knockout mouse (AEG-1

conclusionAEG-1 might be a key molecule regulating initiation and progression of NASH. AEG-1 inhibitory strategies might be developed as a potential therapeutic intervention in NASH patients. (Hepatology 2017;66:466-480).

Indexed as

Gene Expression RegulationAnalysis of VarianceAnimalsBiopsy, NeedleCells, CulturedDiet, High-FatDisease Models, AnimalHepatocytesHumansImmunohistochemistryMembrane GlycoproteinsMiceMice, Inbred CBAMice, TransgenicNon-alcoholic Fatty Liver DiseasePPAR alphaCrisp1 protein, mouseMembrane GlycoproteinsPPAR alpha

Identifiers

PMID28437865
PMCPMC5519412
OpenAlexW2609544081

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.