Evidence map›Paper›PMID 39684236›Full record

ReviewInternational journal of molecular sciences2024

Glioma-Derived Exosomes and Their Application as Drug Nanoparticles.

Serena Mastantuono, Ivana Manini, Carla Di Loreto, Antonio Paolo Beltrami, Marco Vindigni, Daniela Cesselli

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Extracellular vesicles in spine tumors: biological roles, immune modulation, and therapeutic implications.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. 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

6 authors.

Serena MastantuonoDepartment of Medicine, University of Udine, Piazzale S. Maria della Misericordia 15, 33100 Udine, Italy.
Ivana ManiniDepartment of Pathological Anatomy, University Hospital of Udine, Piazzale S. Maria della Misericordia 15, 33100 Udine, Italy.
Carla Di LoretoDepartment of Pathological Anatomy, University Hospital of Udine, Piazzale S. Maria della Misericordia 15, 33100 Udine, Italy.
Antonio Paolo BeltramiDepartment of Medicine, University of Udine, Piazzale S. Maria della Misericordia 15, 33100 Udine, Italy.ORCID 0000-0002-0679-2710
Marco VindigniDepartment of Neurosurgery, University Hospital of Udine, Piazzale S. Maria della Misericordia 15, 33100 Udine, Italy.
Daniela CesselliDepartment of Medicine, University of Udine, Piazzale S. Maria della Misericordia 15, 33100 Udine, Italy.ORCID 0000-0002-0562-7852

Funding

PRIN tArgeting glioma invasion: an additional weapon to impRove theRapeutic Efficacy towards glioblastoma ARREST G53D23003680006Progetto GLIOMI FVG L.R. 13-2021 G25F21002420005
6 · The paper itself

Abstract

Glioblastoma Multiforme (GBM) is the most aggressive primary tumor of the Central Nervous System (CNS) with a low survival rate. The malignancy of GBM is sustained by a bidirectional crosstalk between tumor cells and the Tumor Microenvironment (TME). This mechanism of intercellular communication is mediated, at least in part, by the release of exosomes. Glioma-Derived Exosomes (GDEs) work, indeed, as potent signaling particles promoting the progression of brain tumors by inducing tumor proliferation, invasion, migration, angiogenesis and resistance to chemotherapy or radiation. Given their nanoscale size, exosomes can cross the blood-brain barrier (BBB), thus becoming not only a promising biomarker to predict diagnosis and prognosis but also a therapeutic target to treat GBM. In this review, we describe the structural and functional characteristics of exosomes and their involvement in GBM development, diagnosis, prognosis and treatment. In addition, we discuss how exosomes can be modified to be used as a therapeutic target/drug delivery system for clinical applications.

Indexed as

Brain NeoplasmsExosomesNanoparticlesAnimalsAntineoplastic AgentsBlood-Brain BarrierDrug Delivery SystemsGlioblastomaGliomaHumansTumor MicroenvironmentAntineoplastic Agentsexosomesglioblastoma multiformeglioma-derived exosomestumor microenvironment

Identifiers

PMID39684236
PMCPMC11641060

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.