Evidence map›Paper›PMID 42181976›Full record

ReviewInternational journal of nanomedicine2026

Therapeutic Potential of Mesenchymal Stem Cell-Derived Extracellular Vesicles in Digestive System Tumors: Modulating the Chronic Inflammatory Microenvironment.

Huapei Kang, Tao Ding, Haihong Lin, Fangsheng Wang, Yifan Zhu, Puwen Chen, Hanlu Chen, Junyun Huang, Xiaoling Wang

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 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.

Huapei Kang *The First School of Clinical Medicine, Gannan Medical University, Ganzhou, People's Republic of China.ORCID 0009-0001-7790-0205
Tao Ding *The First School of Clinical Medicine, Gannan Medical University, Ganzhou, People's Republic of China.
Haihong LinLaboratory Medicine, First Affiliated Hospital of Gannan Medical University, Ganzhou, People's Republic of China.
Fangsheng WangThe First School of Clinical Medicine, Gannan Medical University, Ganzhou, People's Republic of China.
Yifan ZhuLaboratory Medicine, First Affiliated Hospital of Gannan Medical University, Ganzhou, People's Republic of China.ORCID 0009-0006-4083-2137
Puwen ChenThe First School of Clinical Medicine, Gannan Medical University, Ganzhou, People's Republic of China.
Hanlu ChenLaboratory Medicine, First Affiliated Hospital of Gannan Medical University, Ganzhou, People's Republic of China.
Junyun HuangThe First School of Clinical Medicine, Gannan Medical University, Ganzhou, People's Republic of China.
Xiaoling WangThe First School of Clinical Medicine, Gannan Medical University, Ganzhou, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Digestive system tumors (including colorectal cancer, hepatocellular carcinoma, and gastric cancer) have become one of the most serious global cancer burdens, and their pathological evolution and chronic inflammatory microenvironments are closely related. Chronic inflammation moves into cancer by angling immune cell infiltration, pro-inflammatory stuff, and aberrant signaling pathways, which advance tumor cell growth factor and burst, hitching a ride. In this context, mesenchymal stem cell-derived extracellular vesicles (MSC-EVs)-naturally occurring nan vesicles enveloped by a bilipidic layer-are loaded with bioactive substances like proteins, miRNAs, which present considerable promise in remodeling the chronic inflammatory microenvironments and arresting tumor development. MSC - EVs have the benefits of low risk of being immunogenic, good biological compatibility, and targeted homing capabilities; however, the main aspect is that they adjust immune cells and interfere with key signaling systems using the bioactive materials that they carry. This can be carried out to modulate the chronic inflammatory environment, and it is also carriers to carry specific loads (miRNAs, chemotherapeutic drugs, etc.) to inhibit the tumor cell biological behavior. However, the potential pro-tumorigenic effects of MSC-EVs under specific conditions cannot be overlooked, as they may also transport cargos that accelerate tumor progression. Similarly, EVs derived from non-mesenchymal sources have been shown to drive malignancy through various signaling mechanisms. Although MSC-EVs have great clinical value, there are still problems such as the standardization of preparation, the standardization of heterogeneity control, and the standardization of safety evaluation. Current engineering modification strategies can enhance the effectiveness of engineering. In the future, innovative combinations of technologies and approaches may even lead to more rapid progress toward translation from the bench to the bedside. This paper mainly discusses MSC-EVs regulation mechanism towards chronic inflammation, and the potential for it to inhibit or promote tumor growth, as well as conducting a systematic review of current research on MSC-EVs as a treatment agent for digestive system tumors. Finally, It outlines challenges in clinical application and future prospects.

Indexed as

Digestive System NeoplasmsExtracellular VesiclesMesenchymal Stem CellsAnimalsHumansInflammationTumor Microenvironmentchronic inflammationdigestive system tumorsextracellular vesiclesimmunomodulationmesenchymal stem cellstargeted therapy

Identifiers

PMID42181976
PMCPMC13196804

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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.