Evidence map›Paper›PMID 42381737›Full record

ReviewFrontiers in molecular neuroscience2026

Extracellular vesicles as nanocarriers in glioblastoma: implications for chemoresistance and immune evasion.

Faezeh Ebrahimi, Taha Rahavi Ezabadi, Hale Asghari, Shima Rajaeinejad, Sahar Jalili, Shokuh Aghamirzaei, Erfan Shahabinejad, Fateme Sadat Kouchakzade, Farid Abbaspour, Abbas Lalegani and 2 more

Abstract readReview
In one paragraph

Review in Frontiers in molecular neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Faezeh EbrahimiStudent Research Committee, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
Taha Rahavi EzabadiStudent Research Committee, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Hale AsghariStudent Research Committee, Department of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Shima RajaeinejadFaculty of Medicine, Medical Branch of Tehran, Islamic Azad University, Tehran, Iran.
Sahar JaliliDepartment of Nursing, School of Nursing and Midwifery, Qazvin University of Medical Sciences, Qazvin, Iran.
Shokuh AghamirzaeiDepartment of Internal Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Erfan ShahabinejadStudent Research Committee, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
Fateme Sadat KouchakzadeStudent Research Committee, Afzalipour Faculty of Medicine, Kerman University of Medical Sciences, Kerman, Iran.
Farid AbbaspourDepartment of International Education, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
Abbas LaleganiSchool of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Ali PirsadeghiStudent Research Committee, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Taral R LunavatSection for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM), the most aggressive primary brain tumor, remains highly resistant to conventional therapies because of its pronounced intratumoral heterogeneity, adaptive plasticity, and complex tumor microenvironment. Increasing evidence indicates that extracellular vesicles (EVs) play central roles in mediating intercellular communication within GBM and contribute to multiple mechanisms associated with therapeutic resistance. This review critically examines the biogenesis, molecular cargo composition, and functional heterogeneity of GBM-derived EVs, with particular emphasis on their involvement in chemoresistance-related processes, including apoptosis evasion, DNA repair modulation, stemness maintenance, immune reprogramming, metabolic adaptation, and remodeling of the tumor microenvironment. EV-associated cargos, including microRNAs, long non-coding RNAs, circular RNAs, proteins, and lipids, appear to coordinately regulate interconnected resistance networks under therapeutic pressure rather than functioning through isolated pathways. Importantly, this review distinguishes between findings derived from

Indexed as

biomarkerschemoresistancedrug effluxextracellular vesiclesglioblastomaimmune evasiontherapeutic targetstumor microenvironment

Identifiers

PMID42381737
PMCPMC13316789

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Registered trials

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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.