Evidence map›Paper›PMID 39667388›Full record

ArticleAutophagy2025

Rubicon regulates exosome secretion via the non-autophagic pathway.

Kyosuke Yanagawa, Tamotsu Yoshimori

Abstract read
In one paragraph

Article in Autophagy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Rab27: Molecular switch of tumor exosome secretion (Review).International journal of molecular medicine · 2026
    Review
  2. Review
  3. Extracellular vesicles inEXO : beyond the cell · 2026
    Article
  4. 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

2 authors.

Kyosuke YanagawaDepartment of Genetics, Graduate School of Medicine, Osaka University, Suita, Japan.ORCID 0000-0002-9645-5899
Tamotsu YoshimoriDepartment of Genetics, Graduate School of Medicine, Osaka University, Suita, Japan.ORCID 0000-0001-9787-3788

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomes are small extracellular vesicles (EVs), which have the diameter of 50-150 nm and originate from intralumenal vesicles in multivesicular endosomes (MVBs). Exosomes secreted from donor cells are delivered to recipient cells for transferring of exosome cargos, such as proteins, lipids and nucleic acids. The cargo transfer by exosomes has a pivotal role in cell-to-cell communication for many cellular processes; however, the detailed mechanism remains largely elusive. In our recent study, we found that RUBCN/rubicon regulates exosome secretion through endosomal recruitment of WIPI2, which promotes ESCRT-dependent MVB formation. We further showed that this pathway is essential for age-dependent increasing of exosomes, which transfer the pro-senescent microRNAs, including

Indexed as

AutophagyExosomesIntracellular Signaling Peptides and ProteinsAnimalsAutophagy-Related ProteinsCellular SenescenceEndosomal Sorting Complexes Required for TransportEndosomesHumansMicroRNAsMultivesicular BodiesAutophagy-Related ProteinsEndosomal Sorting Complexes Required for TransportIntracellular Signaling Peptides and ProteinsMicroRNAsAgingautophagyexosomeextracellular vesiclemicroRNAsenescence

Identifiers

PMID39667388
PMCPMC12013410

What Socratic 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 Socratic graph.