ArticleAnnals of surgical oncology2025
Evaluation of Exosome-Based Delivery of Tumor-Suppressive microRNAs for Novel Therapy in Peritoneal Dissemination of Gastric Cancer: Evidence from Experimental Animal Models.
Article in Annals of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
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.
Who cites it
2 citing papers in PubMed.
- MicroRNA-VEGF axis in gastric cancer: a novel therapeutic frontier.Discover oncology · 2026Review
- Orchestrating Tumor Metastasis: Exosomes as Master Regulators of the Local and Distant Microenvironment.International journal of biological sciences · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
19 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPeritoneal dissemination poses a critical challenge in advanced gastric cancer and leads to poor outcomes. Exosomes offer a novel platform for the delivery of tumor-suppressive microRNAs (miRNAs). MicroRNA-338-3p (miR-338-3p), a known tumor suppressor, may target tumor cells and enhance the resistance of normal cells to tumor progression. This study evaluated the therapeutic potential of exosomes loaded with miR-338-3p (Exo338) in preventing peritoneal dissemination of gastric cancer.
methodsExosomes loaded with miR-338-3p using Exo-Fect
resultsOverexpression of miR-338-3p inhibited the proliferation and adhesion of gastric cancer cells in vitro. Exosomes derived from tumor cells showed a lower uptake efficiency, whereas those from MeT-5A cells were efficiently taken up by normal mesothelial cells. Exo338 reduced the ability of tumor cells to adhere to normal mesothelial cells. In vivo, Exo338 administration in a peritoneal dissemination model showed a trend toward a reduced tumor burden.
conclusionsExosome-mediated delivery of miR-338-3p offers a promising approach for gastric cancer therapy by reducing tumor adhesion to mesothelial cells. This strategy underscores the potential of exosome-based miRNA therapies for the treatment of advanced gastric cancer.
Indexed as
Identifiers
40715869What Socratic holds
Registered trials
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 Socratic graph.