Evidence map›Paper›PMID 25254217›Full record

ReviewBioMed research international2014

Autophagy: a multifaceted partner in liver fibrosis.

Ariane Mallat, Jasper Lodder, Fatima Teixeira-Clerc, Richard Moreau, Patrice Codogno, Sophie Lotersztajn

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
7.3field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Aspirin Attenuates Liver Fibrosis via Autophagy Induction.Journal of cellular and molecular medicine · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Pien-Tze-Huang alleviates CClFrontiers in pharmacology · 2022
    Article
  16. Article
  17. Autophagy in liver diseases: A review.Molecular aspects of medicine · 2021
    Review
  18. Article
  19. Article
  20. Review
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

6 authors at 2 institutions in 1 country.

Ariane MallatINSERM U955, 94000 Créteil, France ; Université Paris-Est, Faculté de Médecine, UMR-S955, 94000 Créteil, France.
Jasper LodderINSERM U1149, Center for Research on Inflammation, 75018 Paris, France ; Université Paris Diderot, Sorbonne Paris Cité, Faculté de Médecine, Site Xavier Bichat, 75018 Paris, France ; Laboratoire d'Excellence Inflamex, 75018 Paris, France.ORCID 0000-0002-1963-835X
Fatima Teixeira-ClercINSERM U955, 94000 Créteil, France ; Université Paris-Est, Faculté de Médecine, UMR-S955, 94000 Créteil, France.
Richard MoreauINSERM U1149, Center for Research on Inflammation, 75018 Paris, France ; Université Paris Diderot, Sorbonne Paris Cité, Faculté de Médecine, Site Xavier Bichat, 75018 Paris, France ; Laboratoire d'Excellence Inflamex, 75018 Paris, France ; Département Hospitalo-Universitaire (DHU) UNITY, Service d'Hépatologie, Hôpital Beaujon, AP-HP, 92000 Clichy, France.
Patrice CodognoINSERM U1151-CNRS UMR8223, INEM, 75014 Paris, France ; Université Paris-Descartes, Sorbonne Paris Cité, Site Necker Enfants-Malades, 75015 Paris, France.
Sophie LotersztajnINSERM U1149, Center for Research on Inflammation, 75018 Paris, France ; Université Paris Diderot, Sorbonne Paris Cité, Faculté de Médecine, Site Xavier Bichat, 75018 Paris, France ; Laboratoire d'Excellence Inflamex, 75018 Paris, France ; Département Hospitalo-Universitaire (DHU) UNITY, Service d'Hépatologie, Hôpital Beaujon, AP-HP, 92000 Clichy, France.
Inserm · FRDélégation Paris 5 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver fibrosis is a common wound healing response to chronic liver injury of all causes, and its end-stage cirrhosis is responsible for high morbidity and mortality worldwide. Fibrosis results from prolonged parenchymal cell apoptosis and necrosis associated with an inflammatory reaction that leads to recruitment of immune cells, activation and accumulation of fibrogenic cells, and extracellular matrix accumulation. The fibrogenic process is driven by hepatic myofibroblasts, that mainly derive from hepatic stellate cells undergoing a transdifferentiation from a quiescent, lipid-rich into a fibrogenic myofibroblastic phenotype, in response to paracrine/autocrine signals produced by neighbouring inflammatory and parenchymal cells. Autophagy is an important regulator of liver homeostasis under physiological and pathological conditions. This review focuses on recent findings showing that autophagy is a novel, but complex, regulatory pathway in liver fibrosis, with profibrogenic effects relying on its direct contribution to the process of hepatic stellate cell activation, but with antifibrogenic properties via indirect hepatoprotective and anti-inflammatory properties. Therefore, cell-specific delivery of drugs that exploit autophagic pathways is a prerequisite to further consider autophagy as a potential target for antifibrotic therapy.

Indexed as

Anti-Inflammatory AgentsAutophagyCell TransdifferentiationExtracellular MatrixHepatic Stellate CellsHumansInflammationLiverLiver CirrhosisMyofibroblastsAnti-Inflammatory Agents

Identifiers

PMID25254217
PMCPMC4164803
OpenAlexW1983338238

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.