Evidence map›Paper›PMID 33794741›Full record

ReviewAutophagy2022

The ménage à trois of autophagy, lipid droplets and liver disease.

Yasmina Filali-Mouncef, Catherine Hunter, Federica Roccio, Stavroula Zagkou, Nicolas Dupont, Charlotte Primard, Tassula Proikas-Cezanne, Fulvio Reggiori

Open access · greenAbstract readReview
In one paragraph

Review in Autophagy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 189 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
189citing papers in PubMed, 1 pooled it
29.7field-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

189 citing papers in PubMed, 1 synthesis or guideline pooled it, 331 citations in OpenAlex.

  1. Pooled it
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  7. From lipid overload to autophagy collapse: how lipid dysregulation drives chronic inflammation and metabolic disease.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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  16. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
    Article
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  20. Review

129 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 4 institutions in 3 countries.

Yasmina Filali-MouncefDepartment of Cell Biology, University of Groningen, University Medical Center Groningen, AV Groningen, The Netherlands.
Catherine HunterInterfaculty Institute of Cell Biology, Eberhard Karls University Tuebingen, Tuebingen, Germany.
Federica RoccioInstitut Necker Enfants-Malades (INEM), INSERM U1151-CNRS UMR 8253, Université de Paris, Paris, France.
Stavroula ZagkouAdjuvatis, Lyon, France.
Nicolas DupontInstitut Necker Enfants-Malades (INEM), INSERM U1151-CNRS UMR 8253, Université de Paris, Paris, France.
Charlotte PrimardAdjuvatis, Lyon, France.
Tassula Proikas-CezanneInterfaculty Institute of Cell Biology, Eberhard Karls University Tuebingen, Tuebingen, Germany.ORCID 0000-0001-6934-132X
Fulvio ReggioriDepartment of Cell Biology, University of Groningen, University Medical Center Groningen, AV Groningen, The Netherlands.ORCID 0000-0003-2652-2686
Centre National de la Recherche Scientifique · FRMax Planck Institute for Developmental Biology · DEUniversity Medical Center Groningen · NLUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagic pathways cross with lipid homeostasis and thus provide energy and essential building blocks that are indispensable for liver functions. Energy deficiencies are compensated by breaking down lipid droplets (LDs), intracellular organelles that store neutral lipids, in part by a selective type of autophagy, referred to as lipophagy. The process of lipophagy does not appear to be properly regulated in fatty liver diseases (FLDs), an important risk factor for the development of hepatocellular carcinomas (HCC). Here we provide an overview on our current knowledge of the biogenesis and functions of LDs, and the mechanisms underlying their lysosomal turnover by autophagic processes. This review also focuses on nonalcoholic steatohepatitis (NASH), a specific type of FLD characterized by steatosis, chronic inflammation and cell death. Particular attention is paid to the role of macroautophagy and macrolipophagy in relation to the parenchymal and non-parenchymal cells of the liver in NASH, as this disease has been associated with inappropriate lipophagy in various cell types of the liver.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsNon-alcoholic Fatty Liver DiseaseAutophagyHumansLipid DropletsChaperone-mediated autophagyfibrosishepatocellular carcinomamacroautophagymacrolipophagymicroautophagymicrolipophagynafldnashnonalcoholic fatty liver diseasenonalcoholic steatohepatitis

Identifiers

PMID33794741
PMCPMC8865253
OpenAlexW3145371283

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.