Evidence map›Paper›PMID 31171880›Full record

ArticleNature medicine2019

Metagenomic and metabolomic analyses reveal distinct stage-specific phenotypes of the gut microbiota in colorectal cancer.

Shinichi Yachida, Sayaka Mizutani, Hirotsugu Shiroma, Satoshi Shiba, Takeshi Nakajima, Taku Sakamoto, Hikaru Watanabe, Keigo Masuda, Yuichiro Nishimoto, Masaru Kubo and 20 more

Registry-linked trialOpen access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05870696 (Evaluation of the Serum Metabolite Based PrecogColo Dx Test for Advanced Colorectal Neoplasia Screening), which is not on this map. Cited by 828 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
828citing papers in PubMed, 5 pooled it
46.9field-weighted citation impact, top 1% of its field
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.

NCT05870696 unknown statusnot on this mapstarted 2023, after this paper: background citation

Evaluation of the Serum Metabolite Based PrecogColo Dx Test for Advanced Colorectal Neoplasia Screening

TypeobservationalSponsorPeking University Third HospitalRan2023 to 2024Enrolled2,000ConditionsColorectal AdenomaArmsPrecogColo Dx test
3 · Its place in the literature

Who cites it

828 citing papers in PubMed, 5 syntheses or guidelines pooled it, 1,428 citations in OpenAlex.

  1. Colorectal neoplasia-specific amino acid profiles and their diagnostic potential: a systematic review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Pooled it
  2. Global research trends inFrontiers in cellular and infection microbiology · 2026
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Gut Microbial Topology and Metabolic Signatures Associated With Colorectal Neoplasia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Emerging trends in the global burden of colorectal cancer.Nature reviews. Clinical oncology · 2026
    Review
  20. Review

768 more citing papers are in PubMed but not listed here.

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

30 authors at 10 institutions in 2 countries.

Shinichi Yachida *Department of Cancer Genome Informatics, Graduate School of Medicine, Osaka University, Osaka, Japan. syachida@cgi.med.osaka-u.ac.jp.ORCID http://orcid.org/0000-0001-5507-4566
Sayaka Mizutani *School of Life Science and Technology, Tokyo Institute of Technology, Tokyo, Japan.ORCID http://orcid.org/0000-0003-4168-6195
Hirotsugu ShiromaSchool of Life Science and Technology, Tokyo Institute of Technology, Tokyo, Japan.
Satoshi ShibaDivision of Cancer Genomics, National Cancer Center Research Institute, Tokyo, Japan.
Takeshi NakajimaEndoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Taku SakamotoEndoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Hikaru WatanabeSchool of Life Science and Technology, Tokyo Institute of Technology, Tokyo, Japan.
Keigo MasudaSchool of Life Science and Technology, Tokyo Institute of Technology, Tokyo, Japan.
Yuichiro NishimotoSchool of Life Science and Technology, Tokyo Institute of Technology, Tokyo, Japan.
Masaru KuboSchool of Life Science and Technology, Tokyo Institute of Technology, Tokyo, Japan.
Fumie HosodaDivision of Cancer Genomics, National Cancer Center Research Institute, Tokyo, Japan.
Hirofumi RokutanDivision of Cancer Genomics, National Cancer Center Research Institute, Tokyo, Japan.
Minori MatsumotoEndoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Hiroyuki TakamaruEndoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Masayoshi YamadaEndoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Takahisa MatsudaEndoscopy Division, National Cancer Center Hospital, Tokyo, Japan.ORCID http://orcid.org/0000-0002-9244-2820
Motoki IwasakiEpidemiology and Prevention Group, Center for Public Health Sciences, National Cancer Center, Tokyo, Japan.
Taiki YamajiEpidemiology and Prevention Group, Center for Public Health Sciences, National Cancer Center, Tokyo, Japan.
Tatsuo YachidaDepartment of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Tomoyoshi SogaInstitute for Advanced Biosciences, Keio University, Yamagata, Japan.
Ken KurokawaGenome Evolution Laboratory, National Institute of Genetics, Shizuoka, Japan.ORCID http://orcid.org/0000-0001-8662-9958
Atsushi ToyodaComparative Genomics Laboratory, National Institute of Genetics, Shizuoka, Japan.ORCID http://orcid.org/0000-0002-0728-7548
Yoshitoshi OguraDepartment of Bacteriology, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
Tetsuya HayashiDepartment of Bacteriology, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
Masanori HatakeyamaDepartment of Microbiology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Hitoshi NakagamaNational Cancer Center, Tokyo, Japan.
Yutaka SaitoEndoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Shinji FukudaInstitute for Advanced Biosciences, Keio University, Yamagata, Japan.
Tatsuhiro ShibataDivision of Cancer Genomics, National Cancer Center Research Institute, Tokyo, Japan.
Takuji YamadaSchool of Life Science and Technology, Tokyo Institute of Technology, Tokyo, Japan. takuji@bio.titech.ac.jp.ORCID http://orcid.org/0000-0002-9622-1849
National Cancer Center Hospital East · JPTokyo Institute of Technology · JPKyushu University · JPNational Institute of Genetics · JPThe University of Tokyo · JPJapan Science and Technology Agency · JPKagawa University · JPKeio University · JPOsaka City University · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In most cases of sporadic colorectal cancers, tumorigenesis is a multistep process, involving genomic alterations in parallel with morphologic changes. In addition, accumulating evidence suggests that the human gut microbiome is linked to the development of colorectal cancer. Here we performed fecal metagenomic and metabolomic studies on samples from a large cohort of 616 participants who underwent colonoscopy to assess taxonomic and functional characteristics of gut microbiota and metabolites. Microbiome and metabolome shifts were apparent in cases of multiple polypoid adenomas and intramucosal carcinomas, in addition to more advanced lesions. We found two distinct patterns of microbiome elevations. First, the relative abundance of Fusobacterium nucleatum spp. was significantly (P < 0.005) elevated continuously from intramucosal carcinoma to more advanced stages. Second, Atopobium parvulum and Actinomyces odontolyticus, which co-occurred in intramucosal carcinomas, were significantly (P < 0.005) increased only in multiple polypoid adenomas and/or intramucosal carcinomas. Metabolome analyses showed that branched-chain amino acids and phenylalanine were significantly (P < 0.005) increased in intramucosal carcinomas and bile acids, including deoxycholate, were significantly (P < 0.005) elevated in multiple polypoid adenomas and/or intramucosal carcinomas. We identified metagenomic and metabolomic markers to discriminate cases of intramucosal carcinoma from the healthy controls. Our large-cohort multi-omics data indicate that shifts in the microbiome and metabolome occur from the very early stages of the development of colorectal cancer, which is of possible etiological and diagnostic importance.

Indexed as

Gastrointestinal MicrobiomeAdultAgedCase-Control StudiesColorectal NeoplasmsDisease ProgressionFemaleHumansMaleMetabolomicsMetagenomicsMiddle AgedNeoplasm StagingYoung Adult

Identifiers

PMID31171880
OpenAlexW2949004447

What OpenQuestion holds

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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 OpenQuestion graph.