Evidence map›Paper›PMID 42910351›Full record

ReviewMedComm2026

Exosomes in Cancer: The Biology, Function, Diagnosis, and Therapy.

Jun Wu, Lei Wu, Kang Yang, Kang Xie, Tao Lu, Tiangxiang Huang, Dengfeng Wan, Tao Song, Longbo Zhang

Abstract readReview
In one paragraph

Review in MedComm, 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

9 authors.

Jun Wu *Departments of Neurosurgery National Clinical Research Center for Geriatric Disorders (Xiangya Hospital) Central South University Changsha China.
Lei Wu *Department of Neurosurgery The Second Affiliated Hospital of Nanchang University Nanchang China.
Kang Yang *Departments of Neurosurgery National Clinical Research Center for Geriatric Disorders (Xiangya Hospital) Central South University Changsha China.
Kang XieDepartments of Neurosurgery National Clinical Research Center for Geriatric Disorders (Xiangya Hospital) Central South University Changsha China.
Tao LuDepartments of Neurosurgery National Clinical Research Center for Geriatric Disorders (Xiangya Hospital) Central South University Changsha China.
Tiangxiang HuangDepartments of Neurosurgery National Clinical Research Center for Geriatric Disorders (Xiangya Hospital) Central South University Changsha China.
Dengfeng WanDepartments of Neurosurgery National Regional Center for Neurological Diseases Xiangya Hospital Central South University Jiangxi China.
Tao SongDepartments of Neurosurgery National Clinical Research Center for Geriatric Disorders (Xiangya Hospital) Central South University Changsha China.
Longbo ZhangDepartments of Neurosurgery National Clinical Research Center for Geriatric Disorders (Xiangya Hospital) Central South University Changsha China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomes are central mediators of intercellular communication in the tumor microenvironment, transferring proteins, lipids, metabolites, and nucleic acids that regulate cancer progression. Recent advances in multi-omics and extracellular vesicle profiling have revealed substantial molecular and functional heterogeneity, extending beyond classical membrane-bound exosomes to nonmembranous extracellular nanoparticles such as exomeres and supermeres. Here, we provide a pan-cancer synthesis of exosome biology, integrating mechanisms of biogenesis, cargo sorting, and secretion with emerging concepts of extracellular nanoparticle diversity. We examine how tumor-derived exosomes remodel local and distant microenvironments by promoting angiogenesis, metabolic reprogramming, immune suppression, premetastatic niche formation, and cancer-associated cachexia. We also discuss the relative contributions of active organotropic targeting and passive spatiotemporal accumulation to metastatic dissemination, together with tissue-specific mechanisms governing endothelial barrier crossing, myeloid-cell reprogramming, and intercellular network integration. Clinically, we evaluate exosome-based liquid biopsy, molecular subtyping, engineered delivery systems, and strategies that inhibit endogenous vesicle production or circulation. Finally, we outline key translational challenges, including single-vesicle heterogeneity, limited intravital tracking, and the absence of standardized cGMP manufacturing and analytical frameworks across diverse tumor types and clinically relevant biological contexts worldwide. This review defines a roadmap for exosome-guided precision oncology.

Indexed as

biomimetic nanovesiclesexosomesextracellular nanoparticlesmultifluid liquid biopsypan‐cancer hallmarksprecision oncologytherapeutic interception

Identifiers

PMID42910351
PMCPMC13686425

What OpenQuestion holds

Textmetadata
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.