Evidence map›Paper›PMID 38383468›Full record

ArticleNature communications2024

Exosomes define a local and systemic communication network in healthy pancreas and pancreatic ductal adenocarcinoma.

Bárbara Adem, Nuno Bastos, Carolina F Ruivo, Sara Sousa-Alves, Carolina Dias, Patrícia F Vieira, Inês A Batista, Bruno Cavadas, Dieter Saur, José C Machado and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
6.8field-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

18 citing papers in PubMed, 29 citations in OpenAlex.

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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

12 authors at 4 institutions in 3 countries.

Bárbara Ademi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Nuno Bastosi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Carolina F Ruivoi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Sara Sousa-Alvesi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0001-7118-0772
Carolina Diasi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0003-2884-0055
Patrícia F Vieirai3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0002-7289-7625
Inês A Batistai3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0003-0321-7902
Bruno Cavadasi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Dieter SaurMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, Munich, Germany.ORCID 0000-0001-5874-0210
José C Machadoi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Dawen CaiDepartment of Cell and Developmental Biology, Medical School, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0003-4471-2061
Sonia A Meloi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal. smelo@i3s.up.pt.ORCID 0000-0002-2291-4263
Universidade do Porto · PTi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PTGerman Cancer Research Center · DEUniversity of Michigan · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC), a lethal disease, requires a grasp of its biology for effective therapies. Exosomes, implicated in cancer, are poorly understood in living systems. Here we use the genetically engineered mouse model (ExoBow) to map the spatiotemporal distribution of exosomes from healthy and PDAC pancreas in vivo to determine their biological significance. We show that, within the PDAC microenvironment, cancer cells establish preferential communication routes through exosomes with cancer associated fibroblasts and endothelial cells. The latter being a conserved event in the healthy pancreas. Inhibiting exosomes secretion in both scenarios enhances angiogenesis, underscoring their contribution to vascularization and to cancer. Inter-organ communication is significantly increased in PDAC with specific organs as most frequent targets of exosomes communication occurring in health with the thymus, bone-marrow, brain, and intestines, and in PDAC with the kidneys, lungs and thymus. In sum, we find that exosomes mediate an organized intra- and inter- pancreas communication network with modulatory effects in vivo.

Indexed as

Carcinoma, Pancreatic DuctalExosomesPancreatic NeoplasmsAnimalsCell Line, TumorCell MovementEndothelial CellsMicePancreasTumor Microenvironment

Identifiers

PMID38383468
PMCPMC10881969
OpenAlexW4391997444

What OpenQuestion holds

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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.