Evidence map›Paper›PMID 40562928›Full record

ReviewNature2025

The expanding repertoire of ESCRT functions in cell biology and disease.

James H Hurley, Alyssa N Coyne, Marta Miączyńska, Harald Stenmark

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
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

40 citing papers in PubMed.

  1. Mechanisms of HIV-1 assembly, release and maturation.Nature reviews. Microbiology · 2026
    Review
  2. Ferroptosis in liver biology and diseases.Hepatology communications · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Regulation and roles of mammalian mitophagy.Nature reviews. Molecular cell biology · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Structural and molecular principles of DAMP biology.Nature structural & molecular biology · 2026
    Review
  11. Article
  12. Autophagy in Melanoma: Molecular Mechanisms and Therapeutic Perspectives.International journal of molecular sciences · 2026
    Review
  13. Article
  14. bioRxiv : the preprint server for biology · 2026
    Article
  15. Review
  16. Article
  17. Article
  18. Phosphatidylinositol diphosphate binding by ESCRT-III filaments.Proceedings of the National Academy of Sciences of the United States of America · 2026
    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

4 authors.

James H HurleyDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA. jimhurley@berkeley.edu.ORCID 0000-0001-5054-5445
Alyssa N CoyneBrain Science Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0002-3658-5325
Marta MiączyńskaLaboratory of Cell Biology, International Institute of Molecular and Cell Biology in Warsaw, Warsaw, Poland.ORCID 0000-0003-0031-5267
Harald StenmarkDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA. stenmark@ulrik.uio.no.ORCID 0000-0002-1971-4252

Funding

Mechanisms of impaired ESCRT-III nuclear surveillance in ALS/FTDR01NS132836 · NINDS · JOHNS HOPKINS UNIVERSITY · PI Alyssa Coyne · 2023 to 2026
$2.3M
Mechanisms of nuclear pore complex homeostasis and injury in ALS/FTD and related neurodegenerative diseasesR00NS123242 · NINDS · JOHNS HOPKINS UNIVERSITY · PI COYNE, ALYSSA · 2022 to 2024
$747k
NINDS NIH HHS R00 NS123242NINDS NIH HHS R01 NS132836
6 · The paper itself

Abstract

The endosomal sorting complex required for transport (ESCRT) is a multicomplex machinery comprising proteins that are conserved from bacteria to humans and has diverse roles in regulating the dynamics of cellular membranes. ESCRT functions have far-reaching consequences for cell biological processes such as intracellular traffic, membrane repair, cell signalling, metabolic regulation, cell division and genome maintenance. Here we review recent insights that emphasize the pathophysiological consequences of ESCRT dysfunctions, including infections, immune disorders, cancers and neurological diseases. We highlight the possibilities of using our knowledge about ESCRT structures and functions for drug discovery.

Indexed as

DiseaseEndosomal Sorting Complexes Required for TransportAnimalsDrug DiscoveryHumansNeoplasmsNervous System DiseasesEndosomal Sorting Complexes Required for Transport

Identifiers

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.