Evidence map›Paper›PMID 31978536›Full record

ReviewMethods (San Diego, Calif.)2020

Unraveling the mechanisms that specify molecules for secretion in extracellular vesicles.

Andrew M Leidal, Jayanta Debnath

Abstract readReview
In one paragraph

Review in Methods (San Diego, Calif.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
–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

39 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  11. Glioma-Derived Exosomes and Their Application as Drug Nanoparticles.International journal of molecular sciences · 2024
    Review
  12. Article
  13. Article
  14. Review
  15. Article
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  17. Article
  18. Review
  19. Article
  20. Exosomes induce neurogenesis of pluripotent P19 cells.Stem cell reviews and reports · 2023
    Article
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.

Andrew M LeidalDepartment of Pathology and Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA 94143, USA. Electronic address: andrew.leidal@ucsf.edu.
Jayanta DebnathDepartment of Pathology and Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA 94143, USA.

Funding

Endolysosomal defects in secretory autophagy and microglial toxicity in FTDR01AG057462 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jayanta Debnath, Eric J Huang · 2017 to 2026
$6.9M
Autophagy in Adhesion and MetastasisR01CA126792 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jayanta Debnath · 2009 to 2026
$5.3M
Autophagy as a microenvironmental regulator of tumorigenesis and resistanceR01CA188404 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BERGERS, GABRIELE, DEBNATH, JAYANTA · 2014 to 2018
$2.1M
Stromal Fibroblast Autophagy In Tumor Progression and DesmoplasiaR01CA213775 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DEBNATH, JAYANTA · 2018 to 2022
$1.9M
Deciphering Autophagy-Dependent Secretion In Cancer Via Proximity-Based BiotinylationR21CA201849 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DEBNATH, JAYANTA · 2016 to 2017
$379k
SYNAPTIC APOE RECEPTORS IN ALZHEIMER AND CONTROLF32AG005746 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI KIM, TAE-WAN · 1996 to 1997
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CIHR 201409BPF-335868NCI NIH HHS R01 CA126792NCI NIH HHS R01 CA188404NCI NIH HHS R01 CA213775NCI NIH HHS R21 CA201849NIA NIH HHS F32 AG005746NIA NIH HHS R01 AG057462
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are small membrane-bound organelles naturally released from cells and potentially function as vehicles of intercellular communication. Cells release numerous sub-species of EVs, including exosomes and microvesicles, which are formed via distinct cellular pathways and molecular machineries and contain specific proteins, RNAs and lipids. Accumulating evidence indicates that the repertoire of molecules packaged into EVs is shaped by both the physiological state of the cell and the EV biogenesis pathway involved. Although these observations intimate that precisely regulated pathways sort molecules into EVs, the underlying molecular mechanisms that direct molecules for secretion remain poorly defined. Recently, with the advancement of mass spectrometry, next-generation sequencing techniques and molecular biology tools, several mechanisms contributing to EV cargo selection are beginning to be unraveled. This review examines strategies employed to reveal how specific proteins, RNAs and lipids are directed for secretion via EVs.

Indexed as

ArrestinsCell CommunicationEndosomal Sorting Complexes Required for TransportExtracellular VesiclesGene ExpressionHigh-Throughput Nucleotide SequencingHumansLipidsMass SpectrometryNeoplasmsNeurodegenerative DiseasesOrganelle BiogenesisProtein Interaction MappingRNATwo-Hybrid System TechniquesARRDC1 protein, humanArrestinsEndosomal Sorting Complexes Required for TransportLipidsRNACargo: Protein, RNA or lipid species incorporated in to extracellular vesiclesEXOmotif: short RNA sequence that targets microRNAs for secretion in extracellular vesicles

Identifiers

PMID31978536
PMCPMC7198338

What OpenQuestion holds

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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.