Evidence map›Paper›PMID 32481590›Full record

ArticleCells2020

Deletion of Perilipin 5 Protects Against Hepatic Injury in Nonalcoholic Fatty Liver Disease via Missing Inflammasome Activation.

Anastasia Asimakopoulou, Kathrin M Engel, Nikolaus Gassler, Thilo Bracht, Barbara Sitek, Eva M Buhl, Stavroula Kalampoka, Manuela Pinoé-Schmidt, Josef van Helden, Jürgen Schiller and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Molecular medicine reports · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Pharmacotherapy of Liver Fibrosis and Hepatitis: Recent Advances.Pharmaceuticals (Basel, Switzerland) · 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

11 authors at 8 institutions in 2 countries.

Anastasia AsimakopoulouInstitute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry (IFMPEGKC), RWTH University Hospital Aachen, 52074 Aachen, Germany.
Kathrin M EngelInstitute for Medical Physics and Biophysics, Leipzig University, Medical Faculty, 04107 Leipzig, Germany.ORCID 0000-0003-0611-7042
Nikolaus GasslerSection Pathology, Institute of Legal Medicine, University Hospital Jena, 07747 Jena, Germany.
Thilo BrachtRuhr-University Bochum, Medical Faculty, Medizinisches Proteom-Center, 44801 Bochum, Germany.
Barbara SitekRuhr-University Bochum, Medical Faculty, Medizinisches Proteom-Center, 44801 Bochum, Germany.
Eva M BuhlElectron Microscopy Facility, Institute of Pathology, RWTH Aachen University Hospital, 52074 Aachen, Germany.
Stavroula KalampokaInstitute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry (IFMPEGKC), RWTH University Hospital Aachen, 52074 Aachen, Germany.
Manuela Pinoé-SchmidtInstitute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry (IFMPEGKC), RWTH University Hospital Aachen, 52074 Aachen, Germany.
Josef van HeldenLaboratory Mönchengladbach-MVZ Dr. Stein and Colleagues, 41169 Mönchengladbach, Germany.ORCID 0000-0002-6309-8194
Jürgen SchillerInstitute for Medical Physics and Biophysics, Leipzig University, Medical Faculty, 04107 Leipzig, Germany.
Ralf WeiskirchenInstitute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry (IFMPEGKC), RWTH University Hospital Aachen, 52074 Aachen, Germany.ORCID 0000-0003-3888-0931
Universitätsklinikum Aachen · DELeipzig University · DEJena University Hospital · DERuhr University Bochum · DERWTH Aachen University · DEStädtische Kliniken Mönchengladbach · DEUniversitätsklinikum Knappschaftskrankenhaus Bochum · DEUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver diseases with an increasing prevalence due to rising rates of obesity, metabolic syndrome and type II diabetes. Untreated NAFLD may progress to steatohepatitis (NASH) and ultimately liver cirrhosis. NAFLD is characterized by lipid accumulation, and when sufficient excess lipids are obtained, irreversible liver injury may follow. Perilipin 5 (PLIN5), a known lipid droplet coating protein and triglyceride metabolism regulator, is highly expressed in oxidatively modified tissues but it is still unclear how it affects NAFLD/NASH progress. We here studied how PLIN5 affects NAFLD development induced by a 30-week high-fat diet (HFD) administration in wild type and PLIN5 knock out (

Indexed as

Gene DeletionAnimalsArachidonic AcidDiet, High-FatEndoplasmic Reticulum StressFemaleHepatocytesInflammasomesInflammationLipid MetabolismLiverMice, Inbred C57BLMitochondria, LiverNLR Family, Pyrin Domain-Containing 3 ProteinNon-alcoholic Fatty Liver DiseasePerilipin-5Arachidonic AcidInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mousePerilipin-5hepatocytesinflammasomeinflammationlipid dropletsliverNAFLDNASHNLRP3PLIN5steatohepatitis

Identifiers

PMID32481590
PMCPMC7348929
OpenAlexW3029585481

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.