Evidence map›Paper›PMID 37514090›Full record

ReviewPharmaceutics2023

New Possible Ways to Use Exosomes in Diagnostics and Therapy via JAK/STAT Pathways.

Gréta Gombos, Nikolett Németh, Ondrej Pös, Jakub Styk, Gergely Buglyó, Tomas Szemes, Ludovit Danihel, Bálint Nagy, István Balogh, Beáta Soltész

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2023. 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
0.9field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. 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

10 authors at 3 institutions in 2 countries.

Gréta GombosDepartment of Human Genetics, Faculty of Medicine, University of Debrecen, Egyetem Tér 1, H-4032 Debrecen, Hungary.ORCID 0009-0006-8062-8560
Nikolett NémethDepartment of Human Genetics, Faculty of Medicine, University of Debrecen, Egyetem Tér 1, H-4032 Debrecen, Hungary.
Ondrej PösComenius University Science Park, 841 04 Bratislava, Slovakia.ORCID 0000-0003-2491-2285
Jakub StykComenius University Science Park, 841 04 Bratislava, Slovakia.ORCID 0000-0002-5717-3522
Gergely BuglyóDepartment of Human Genetics, Faculty of Medicine, University of Debrecen, Egyetem Tér 1, H-4032 Debrecen, Hungary.
Tomas SzemesComenius University Science Park, 841 04 Bratislava, Slovakia.
Ludovit Danihel3rd Surgical Clinic, Faculty of Medicine, Comenius University and Merciful Brothers University Hospital, 811 08 Bratislava, Slovakia.
Bálint NagyDepartment of Human Genetics, Faculty of Medicine, University of Debrecen, Egyetem Tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0002-0295-185X
István BaloghDepartment of Human Genetics, Faculty of Medicine, University of Debrecen, Egyetem Tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0003-3397-2829
Beáta SoltészDepartment of Human Genetics, Faculty of Medicine, University of Debrecen, Egyetem Tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0002-0037-2774
University of Debrecen · HUGeneton (Slovakia) · SKComenius University Bratislava · SK

Funding

Operational Programme Integrated Infrastructure for the project PreveLynch, co-financed by the European Regional Development Fund ITMS: 313011V578
6 · The paper itself

Abstract

Exosomes have the potential to be the future of personalized diagnostics and therapy. They are nano-sized particles between 30 and 100 nm flowing in the extracellular milieu, where they mediate cell-cell communication and participate in immune system regulation. Tumor-derived exosomes (TDEs) secreted from different types of cancer cells are the key regulators of the tumor microenvironment. With their immune suppressive cargo, TDEs prevent the antitumor immune response, leading to reduced effectiveness of cancer treatment by promoting a pro-tumorigenic microenvironment. Involved signaling pathways take part in the regulation of tumor proliferation, differentiation, apoptosis, and angiogenesis. Signal transducers and activators of transcription factors (STATs) and Janus kinase (JAK) signaling pathways are crucial in malignancies and autoimmune diseases alike, and their potential to be manipulated is currently the focus of interest. In this review, we aim to discuss exosomes, TDEs, and the JAK/STAT pathways, along with mediators like interleukins, tripartite motif proteins, and interferons.

Indexed as

cancerexosomesJAK/STAT pathwaysTRIMtumor-derived exosomes

Identifiers

PMID37514090
PMCPMC10386711
OpenAlexW4383818920

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.