Evidence map›Paper›PMID 23774882›Full record

ReviewAutophagy2013

Functions of autophagy in normal and diseased liver.

Mark J Czaja, Wen-Xing Ding, Terrence M Donohue, Scott L Friedman, Jae-Sung Kim, Masaaki Komatsu, John J Lemasters, Antoinette Lemoine, Jiandie D Lin, Jing-hsiung James Ou and 5 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Autophagy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 258 papers.

0numbers the graph read from it
0cells of the map it votes in
258citing papers in PubMed
21.8field-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

258 citing papers in PubMed, 437 citations in OpenAlex.

  1. E3 Ubiquitin Ligases in MASH-Associated Liver Fibrosis: Mechanisms and Therapeutic Opportunities.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Aspirin Attenuates Liver Fibrosis via Autophagy Induction.Journal of cellular and molecular medicine · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Mutations in fibronectin dysregulate chondrogenesis in skeletal dysplasia.Cellular and molecular life sciences : CMLS · 2024
    Article
  17. Article
  18. Review
  19. Organophosphate ester flame retardants and plasticizers affect the phenotype and function of HepG2 liver cells.Toxicological sciences : an official journal of the Society of Toxicology · 2024
    Article
  20. Article

198 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

15 authors at 14 institutions in 5 countries.

Mark J CzajaDepartment of Medicine; Marion Bessin Liver Research Center; Albert Einstein College of Medicine; Bronx, NY USA.
Wen-Xing Ding
Terrence M Donohue
Scott L Friedman
Jae-Sung Kim
Masaaki Komatsu
John J Lemasters
Antoinette Lemoine
Jiandie D Lin
Jing-hsiung James Ou
David H Perlmutter
Glenn Randall
Ratna B Ray
Allan Tsung
Xiao-Ming Yin
University of Pittsburgh · USAlbert Einstein College of Medicine · USDépartement de Chimie Moléculaire · FRIndianapolis Zoo · USMedical University of South Carolina · USNew York Proton Center · USTokyo Metropolitan Institute of Medical Science · JPUniversity of Chicago · USUniversity of Florida · USUniversity of Kansas Medical Center · USUniversity of Michigan · USUniversity of Missouri–St. Louis · USUniversity of Nebraska at Omaha · USUniversity of Southern California · US

Funding

Vaccines and Therapies Against BotulismU54AI057153 · NIAID · UNIVERSITY OF CHICAGO · PI SHUMAN, HOWARD A · 2003 to 2013
$87.6M
Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
University of Florida Older Americans Independence Center (OAIC)P30AG028740 · NIA · UNIVERSITY OF FLORIDA · PI CHRISTIAAN LEEUWENBURGH · 2007 to 2026
$22.8M
SOUTH CAROLINA COBRE IN OXIDANTS, REDOX BALANCE AND STRESS SIGNALINGP20GM103542 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI TEW, KENNETH D. · 2012 to 2020
$20.2M
Treating AT Deficiency with Drugs that Modulate the Proteostasis NetworkP01DK096990 · NIDDK · WASHINGTON UNIVERSITY · PI PERLMUTTER, DAVID H · 2012 to 2023
$18.3M
THE ROLE OF HUMAN PXR IN ANTI-TUBERCULOSIS DRUG-INDUCED LIVER INJURYP20RR021940 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI KLASSEN, CURTIS D · 2006 to 2011
$12.1M
TRIM mediated host antiviral responses during influenza virus infectionsU19AI083025 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OU, J.-H. JAMES · 2009 to 2013
$10.0M
MODULATION OF ACUTE TOXIC LIVER INJURYR01DK044234 · NIDDK · YESHIVA UNIVERSITY · PI SRINIVASAN, SHANTHI K · 1992 to 2023
$7.6M
The Role of KLF6 in Hepatic FibrosisR01DK056621 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI FRIEDMAN, SCOTT L. · 2000 to 2019
$6.2M
Virus-host interactions in hepatocarcinogenesisP01CA123328 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LAI, MICHAEL M.C. · 2007 to 2011
$5.3M
Autophagy in liver injuryR01DK079879 · NIDDK · WASHINGTON UNIVERSITY · PI Jae-Sung Kim · 2009 to 2026
$5.0M
Howard Hughes Medical InstituteNCI NIH HHS CA083817NCI NIH HHS CA119079NCI NIH HHS CA123328NCI NIH HHS CA138313NCI NIH HHS P01 CA123328NCI NIH HHS P30 CA138313NCI NIH HHS R01 CA083817NCI NIH HHS R01 CA119079NCI NIH HHS R01 CA177337NCRR NIH HHS C06 RR015455NCRR NIH HHS P20 RR021940NCRR NIH HHS RR015455NCRR NIH HHS RR021940NHLBI NIH HHS HL097738NHLBI NIH HHS R01 HL097738NIAAA NIH HHS AA020518NIAAA NIH HHS AA020709NIAAA NIH HHS R01 AA020518NIAAA NIH HHS R01 AA020709NIAAA NIH HHS R37 AA020518NIAID NIH HHS AI057153NIAID NIH HHS AI080703NIAID NIH HHS AI083025NIAID NIH HHS R01 AI080703NIAID NIH HHS R56 AI080703NIAID NIH HHS U19 AI083025NIAID NIH HHS U54 AI057153NIA NIH HHS AG028740NIA NIH HHS P30 AG028740NIDDK NIH HHS DK037034NIDDK NIH HHS DK044234NIDDK NIH HHS DK056621NIDDK NIH HHS DK061498NIDDK NIH HHS DK073336,NIDDK NIH HHS DK076918NIDDK NIH HHS DK077086NIDDK NIH HHS DK079879NIDDK NIH HHS DK081817NIDDK NIH HHS DK084512NIDDK NIH HHS DK090115NIDDK NIH HHS DK094652NIDDK NIH HHS DK096990NIDDK NIH HHS P01 DK096990NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK037034NIDDK NIH HHS R01 DK044234NIDDK NIH HHS R01 DK056621NIDDK NIH HHS R01 DK061498NIDDK NIH HHS R01 DK073336NIDDK NIH HHS R01 DK076918NIDDK NIH HHS R01 DK077086NIDDK NIH HHS R01 DK079879NIDDK NIH HHS R01 DK081817NIDDK NIH HHS R01 DK084512NIDDK NIH HHS R01 DK090115NIDDK NIH HHS R01 DK094652NIDDK NIH HHS R01 DK100257NIDDK NIH HHS R37 DK037034NIDDK NIH HHS R56 DK037034NIDDK NIH HHS R56 DK044234NIDDK NIH HHS R56 DK056621NIGMS NIH HHS GM095566NIGMS NIH HHS GM103542NIGMS NIH HHS P20 GM103542NIGMS NIH HHS R01 GM095566
6 · The paper itself

Abstract

Autophagy has emerged as a critical lysosomal pathway that maintains cell function and survival through the degradation of cellular components such as organelles and proteins. Investigations specifically employing the liver or hepatocytes as experimental models have contributed significantly to our current knowledge of autophagic regulation and function. The diverse cellular functions of autophagy, along with unique features of the liver and its principal cell type the hepatocyte, suggest that the liver is highly dependent on autophagy for both normal function and to prevent the development of disease states. However, instances have also been identified in which autophagy promotes pathological changes such as the development of hepatic fibrosis. Considerable evidence has accumulated that alterations in autophagy are an underlying mechanism of a number of common hepatic diseases including toxin-, drug- and ischemia/reperfusion-induced liver injury, fatty liver, viral hepatitis and hepatocellular carcinoma. This review summarizes recent advances in understanding the roles that autophagy plays in normal hepatic physiology and pathophysiology with the intent of furthering the development of autophagy-based therapies for human liver diseases.

Indexed as

AutophagyAnimalsCircadian RhythmHumansLipid MetabolismLiverLiver DiseasesModels, Biologicalautophagydrug toxicityhepatitishepatocellular carcinomahepatocytehepatotoxinischemia/reperfusionliverliver injury

Identifiers

PMID23774882
PMCPMC3748187
OpenAlexW2111754392

What OpenQuestion holds

Textmetadata
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.