Evidence map›Paper›PMID 39054623›Full record

ArticleCancer research and treatment2025

Fecal Microbial Dysbiosis Is Associated with Colorectal Cancer Risk in a Korean Population.

Jeongseon Kim, Madhawa Gunathilake, Hyun Yang Yeo, Jae Hwan Oh, Byung Chang Kim, Nayoung Han, Bun Kim, Hyojin Pyun, Mi Young Lim, Young-Do Nam and 1 more

Abstract read
In one paragraph

Article in Cancer research and treatment, 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. Article
  2. Tumor tissue-associatedFrontiers in cellular and infection microbiology · 2026
    Article
  3. Article
  4. Article
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

11 authors.

Jeongseon KimDepartment of Cancer Biomedical Science, Graduate School of Cancer Science and Policy, National Cancer Center, Goyang, Korea.
Madhawa GunathilakeDepartment of Cancer Biomedical Science, Graduate School of Cancer Science and Policy, National Cancer Center, Goyang, Korea.
Hyun Yang YeoDepartment of Cancer Diagnostics, Research Institute, National Cancer Center, Goyang, Korea.
Jae Hwan OhCenter for Colorectal Cancer, National Cancer Center Hospital, National Cancer Center, Goyang, Korea.
Byung Chang KimCenter for Colorectal Cancer, National Cancer Center Hospital, National Cancer Center, Goyang, Korea.
Nayoung HanDepartment of Pathology, National Cancer Center Hospital, National Cancer Center, Goyang, Korea.
Bun KimDepartment of Cancer Diagnostics, Research Institute, National Cancer Center, Goyang, Korea.
Hyojin PyunDepartment of Cancer Biomedical Science, Graduate School of Cancer Science and Policy, National Cancer Center, Goyang, Korea.
Mi Young LimPersonalized Diet Research Group, Food Functionality Research Division, Korea Food Research Institute, Wanju, Korea.
Young-Do NamPersonalized Diet Research Group, Food Functionality Research Division, Korea Food Research Institute, Wanju, Korea.
Hee Jin ChangDepartment of Cancer Diagnostics, Research Institute, National Cancer Center, Goyang, Korea.

Funding

Korea Food Research Institute E0170600-07Ministry of Science and ICTNational Cancer Center 1710880National Cancer Center 2310490
6 · The paper itself

Abstract

purposeThe association between the fecal microbiota and colorectal cancer (CRC) risk has been suggested in epidemiologic studies. However, data from large-scale population-based studies are lacking. MATERIALS AND

methodsIn this case-control study, we recruited 283 CRC patients from the Center for Colorectal Cancer, National Cancer Center Hospital, Korea to perform 16S rRNA gene sequencing of fecal samples. A total of 283 age- and sex-matched healthy participants were selected from 890 cohort of healthy Koreans that are publicly available (PRJEB33905). The microbial dysbiosis index (MDI) was calculated based on the differentially abundant species. The association between MDI and CRC risk was observed using conditional logistic regression. Sparse Canonical Correlation Analysis was performed to integrate species data with microbial pathways obtained by PICRUSt2.

resultsThere is a significant divergence of the microbial composition between CRC patients and controls (permutational multivariate analysis of variance p=0.001). Those who were in third tertile of the MDI showed a significantly increased risk of CRC in the total population (odds ratio [OR], 6.93; 95% confidence interval [CI], 3.98 to 12.06; p-trend < 0.001) compared to those in the lowest tertile. Similar results were found for men (OR, 6.28; 95% CI, 3.04 to 12.98; p-trend < 0.001) and women (OR, 7.39; 95% CI, 3.10 to 17.63; p-trend < 0.001). Bacteroides coprocola and Bacteroides plebeius species and 12 metabolic pathways were interrelated in healthy controls that explain 91% covariation across samples.

conclusionDysbiosis in the fecal microbiota may be associated with an increased risk of CRC. Due to the potentially modifiable nature of the gut microbiota, our findings may have implications for CRC prevention among Koreans.

Indexed as

Colorectal NeoplasmsDysbiosisFecesGastrointestinal MicrobiomeAdultAgedCase-Control StudiesFemaleHumansMaleMiddle AgedRepublic of KoreaRisk FactorsRNA, Ribosomal, 16SRNA, Ribosomal, 16S16S rRNA gene sequencingColorectal neoplasmsFecal microbiomeMicrobial dysbiosisMicrobial metabolic pathways

Identifiers

PMID39054623
PMCPMC11729318

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.