Evidence map›Paper›PMID 40516061›Full record

ArticleClinical and translational science2025

Evaluation of Organoid-Derived Exosomal microRNA as Liquid Biopsy for Colorectal Cancer: A Multicenter Cross-Sectional Study.

Atsuhiro Sasaki, Masatake Kuroha, Masaki Tosa, Seiichi Takahashi, Shinya Oomori, Eiki Nomura, Tatsuya Kikuchi, Motoyuki Onodera, Yuichiro Sato, Teruko Miyazawa and 18 more

Abstract readMulticenter Study
In one paragraph

Article in Clinical and translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
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

28 authors.

Atsuhiro SasakiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Masatake KurohaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.ORCID 0000-0001-7614-9977
Masaki TosaDepartment of Gastroenterology, Iwaki City Medical Center, Iwaki, Japan.
Seiichi TakahashiDepartment of Gastroenterology, Iwaki City Medical Center, Iwaki, Japan.
Shinya OomoriDepartment of Gastroenterology, Japanese Red Cross Sendai Hospital, Sendai, Japan.
Eiki NomuraDepartment of Gastroenterology, Sendai City Hospital, Sendai, Japan.
Tatsuya KikuchiDepartment of Gastroenterology, Sendai City Hospital, Sendai, Japan.
Motoyuki OnoderaDepartment of Gastroenterology, Osaki Citizen Hospital, Osaki, Japan.
Yuichiro SatoDepartment of Gastroenterology, Osaki Citizen Hospital, Osaki, Japan.
Teruko MiyazawaDepartment of Gastroenterology, Japan Community Healthcare Organization, Sendai South Hospital, Sendai, Japan.
Hirofumi ChibaDepartment of Gastroenterology, Iwate Prefectural Isawa Hospital, Oshu, Japan.
Naonobu YokoyamaDepartment of Gastroenterology, Iwate Prefectural Iwai Hospital, Ichinoseki, Japan.
Jun KusakaDepartment of Gastroenterology, Miyagi Cancer Center, Natori, Japan.
Daisuke OkamotoDepartment of Gastroenterology, Shirakawa Kosei General Hospital, Shirakawa, Japan.
Tomoyuki HandaDepartment of Internal Medicine, Kurihara Central Hospital, Kurihara, Japan.
Mikako SugimuraDepartment of Gastroenterology, NHO Sendai Medical Center, Sendai, Japan.
Masahiro IwabuchiDepartment of Gastroenterology, NHO Sendai Medical Center, Sendai, Japan.
Keiichiro HiramotoDepartment of Gastroenterology, South Miyagi Medical Center, Ohgawara, Japan.
Hidekazu ShirotaDepartment of Medical Oncology, Tohoku University Hospital, Sendai, Japan.
Hideya IwakiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hiroshi NagaiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yusuke ShimoyamaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Takeo NaitoDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Rintaro MoroiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hisashi ShigaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yoichi KakutaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.ORCID 0000-0002-7042-009X
Yoshitaka KinouchiStudent Healthcare Center, Institute for Excellence in Higher Education, Tohoku University, Sendai, Japan.
Atsushi MasamuneDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomal microRNAs (miRNAs) are candidates for liquid biopsies. Organoid culture systems enable long-term expansion of the colon epithelium. This study evaluated exosomal miRNAs from colorectal cancer organoids for liquid biopsy. Organoids were established from normal colon and colorectal cancer tissues. Exosomes were isolated from conditioned media. miRNAs were extracted from exosomes and compared using microarray analysis. Exosomal miRNAs expression levels in the sera of healthy patients and patients with colorectal cancer were compared at a single institution. The multicenter study was validated using miRNAs upregulated in the serum of colorectal cancer patients, along with exosomal miRNAs reported to be upregulated in colorectal adenoma organoids and sera. A total of 44 exosomal miRNAs were commonly expressed in both normal colorectal epithelial cells and colorectal cancer organoids, whereas 59 were exclusively expressed in colorectal cancer organoids. In a single-center cohort study, two exosomal miRNAs (miR-4284 and miR-5100) were upregulated in the serum of colorectal cancer patients. In a multicenter study, four exosomal miRNAs (miR-4284, miR-5100, miR-1246, and miR-1290) were upregulated in the serum of patients with colorectal cancer. The combination of these four exosomal miRNAs had comparable diagnostic performance to carcinoembryonic antigen, with an area under the curve of 0.75 (95% confidence interval: 0.65-0.83) versus 0.79 (95% confidence interval: 0.70-0.87). Combining the four miRNAs with carcinoembryonic antigen improved diagnostic accuracy, with an area under the curve of 0.82 (95% confidence interval: 0.74-0.89). Exosomal miRNAs derived from colorectal cancer organoids can serve as diagnostic biomarkers for colorectal cancer.

Indexed as

Biomarkers, TumorColorectal NeoplasmsExosomesMicroRNAsOrganoidsAgedCross-Sectional StudiesFemaleGene Expression Regulation, NeoplasticHumansLiquid BiopsyMaleMiddle AgedBiomarkers, TumorMicroRNAscarcinoembryonic antigenmiR‐1246miR‐1290miR‐4284miR‐5100

Identifiers

PMID40516061
PMCPMC12166945

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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.