Evidence map›Paper›PMID 40985903›Full record

ArticleJournal of extracellular vesicles2025

Genome-Wide CRISPR/Cas9 Screening Identifies the COMMANDER Recycling Complex as a Key Player in EV Uptake.

Miguel Palma-Cobo, Victor Toribio, Joaquín Morales, Soraya López-Martín, Carlos Enrich, Albert Lu, María Yáñez-Mó

Abstract read
In one paragraph

Article in Journal of extracellular vesicles, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Miguel Palma-CoboCentro de Biología Molecular Severo Ochoa, IIS-IP, Universidad Autónoma de Madrid, IUBM, Madrid, Spain.
Victor ToribioCentro de Biología Molecular Severo Ochoa, IIS-IP, Universidad Autónoma de Madrid, IUBM, Madrid, Spain.
Joaquín MoralesCentro de Biología Molecular Severo Ochoa, IIS-IP, Universidad Autónoma de Madrid, IUBM, Madrid, Spain.
Soraya López-MartínCentro de Biología Molecular Severo Ochoa, IIS-IP, Universidad Autónoma de Madrid, IUBM, Madrid, Spain.
Carlos EnrichDepartament de Biomedicina, Unitat de Biologia Cel·lular, Facultat de Medicina i Ciències de la Salut, Centre de Recerca Biomèdica CELLEX, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Universitat de Barcelona, Barcelona, Spain.
Albert LuDepartament de Biomedicina, Unitat de Biologia Cel·lular, Facultat de Medicina i Ciències de la Salut, Centre de Recerca Biomèdica CELLEX, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Universitat de Barcelona, Barcelona, Spain.
María Yáñez-MóCentro de Biología Molecular Severo Ochoa, IIS-IP, Universidad Autónoma de Madrid, IUBM, Madrid, Spain.ORCID https://orcid.org/0000-0001-7484-2866

Funding

Comunidad de MadridFPI-UAM PIF2023/SAL-GL-29726GEIVEXMinisterio Español de Ciencia e InnovaciónPIPF-2023/SAL-GL- 29726Universidad Autónoma de Madrid
6 · The paper itself

Abstract

Extracellular vesicles (EVs) hold immense potential in therapeutic delivery, warranting a comprehensive investigation of the mechanisms that regulate their uptake by target cells. To identify key molecular regulators of EV internalization, we conducted a genome-wide CRISPR (GWC) screen aimed to pinpoint candidate genes that influence EV uptake. We employed a GWC library spanning the entire human genome in K562 cells. 3.6 × 10

Indexed as

CRISPR-Cas SystemsExtracellular VesiclesCell Line, TumorGenome, HumanHeLa CellsHumansK562 CellsMelanomacargo deliveryCOMMANDER complexEV uptakegenome‐wide screen

Identifiers

PMID40985903
PMCPMC12456102

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.