Evidence map›Paper›PMID 41906796›Full record

ArticleCancer science2026

Utility of Urinary Extracellular Vesicles for Colorectal Cancer: Comparison of DNA Quality and MRD Detection.

Shintaro Kanaka, Takeshi Yamada, Fumi Asai, Yuta Shimizu, Kay Uehara, Akihisa Matsuda, Seiichi Shinji, Yasuyuki Yokoyama, Goro Takahashi, Takuma Iwai and 5 more

Abstract readComparative Study
In one paragraph

Article in Cancer science, 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

15 authors.

Shintaro KanakaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9466-2229
Takeshi YamadaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0002-1436-7482
Fumi AsaiH.U. Group Research Institute, G. K., Tokyo, Japan.
Yuta ShimizuH.U. Group Research Institute, G. K., Tokyo, Japan.
Kay UeharaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Akihisa MatsudaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Seiichi ShinjiDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9204-6393
Yasuyuki YokoyamaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Goro TakahashiDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Takuma IwaiDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Kohki TakedaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4528-0742
Sho KuriyamaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Toshimitsu MiyasakaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4066-0479
Koki HayashiDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Hiroshi YoshidaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study evaluated the feasibility of urinary extracellular vesicles (EVs) as a liquid biopsy source for colorectal cancer (CRC) using two predefined cohorts: 97 patients for analytical validation and 63 patients for postoperative survival analysis. We compared urinary EVs, urinary cell-free tumor DNA (ctDNA), plasma EVs, and plasma ctDNA across multiple molecular dimensions, and assessed the utility of urinary EV-DNA for minimal residual disease (MRD) detection. Urinary EVs exhibited larger particle size (median 175.6 nm) and markedly higher purity, demonstrated by a substantially broader proteomic profile (4674 vs. 476 proteins) and significantly higher expression of EV-specific markers (CD63, CD81, CD9). DNA extracted from urinary EVs showed the highest concentration and best preservation of nucleic acid integrity, with the greatest Long/Short fragment ratio, outperforming all plasma-derived samples. Mutation detection sensitivity was comparable across sample types but was highest in plasma ctDNA (39.2%) and urinary EV-DNA (34.0%), exceeding urinary ctDNA (21.6%). In the survival cohort, MRD positivity-defined as detectable RAS/BRAF mutations in urinary EV-DNA 1 month after curative surgery-was strongly associated with inferior outcomes (HR for recurrence 5.25, 95% CI 1.74-15.80), and overall survival was significantly worse in MRD-positive patients. These findings indicate that urinary EVs provide highly pure vesicles with superior DNA quality, making them a robust and completely non-invasive source for molecular profiling. Urinary EV-DNA-based MRD assessment shows significant prognostic value and may serve as a practical tool for postoperative monitoring and risk stratification in colorectal cancer.

Indexed as

Circulating Tumor DNAColorectal NeoplasmsExtracellular VesiclesNeoplasm, ResidualAgedBiomarkers, TumorFemaleHumansLiquid BiopsyMaleMiddle AgedMutationPrognosisBiomarkers, TumorCirculating Tumor DNAcolorectal cancerextracellular vesicleliquid biopsyminimal residual diseaseurine

Identifiers

PMID41906796
PMCPMC13580809

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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.