Evidence map›Paper›PMID 33273632›Full record

ArticleScientific reports2020

Urinary charged metabolite profiling of colorectal cancer using capillary electrophoresis-mass spectrometry.

Ryutaro Udo, Kenji Katsumata, Hiroshi Kuwabara, Masanobu Enomoto, Tetsuo Ishizaki, Makoto Sunamura, Yuichi Nagakawa, Ryoko Soya, Masahiro Sugimoto, Akihiko Tsuchida

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Energy Metabolism Profiling of Human Colorectal Tumours.Journal of cellular and molecular medicine · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Observational
  13. Review
  14. Implication of gut microbes and its metabolites in colorectal cancer.Journal of cancer research and clinical oncology · 2023
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

10 authors.

Ryutaro UdoDepartment of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, 6-7-1, Nishijinjuku, Shinjuku, Tokyo, 160-0023, Japan.
Kenji KatsumataDepartment of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, 6-7-1, Nishijinjuku, Shinjuku, Tokyo, 160-0023, Japan.
Hiroshi KuwabaraDepartment of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, 6-7-1, Nishijinjuku, Shinjuku, Tokyo, 160-0023, Japan.
Masanobu EnomotoDepartment of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, 6-7-1, Nishijinjuku, Shinjuku, Tokyo, 160-0023, Japan.
Tetsuo IshizakiDepartment of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, 6-7-1, Nishijinjuku, Shinjuku, Tokyo, 160-0023, Japan.
Makoto SunamuraDepartment of Gastroenterological Surgery and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachioji City, Tokyo, 193-0998, Japan.
Yuichi NagakawaDepartment of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, 6-7-1, Nishijinjuku, Shinjuku, Tokyo, 160-0023, Japan.
Ryoko SoyaDepartment of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, 6-7-1, Nishijinjuku, Shinjuku, Tokyo, 160-0023, Japan.
Masahiro SugimotoInstitute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata, 997-0811, Japan. mshrsgmt@tokyo-med.ac.jp.ORCID 0000-0003-3316-2543
Akihiko TsuchidaDepartment of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, 6-7-1, Nishijinjuku, Shinjuku, Tokyo, 160-0023, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) has increasing global prevalence and poor prognostic outcomes, and the development of low- or less invasive screening tests is urgently required. Urine is an ideal biofluid that can be collected non-invasively and contains various metabolite biomarkers. To understand the metabolomic profiles of different stages of CRC, we conducted metabolomic profiling of urinary samples. Capillary electrophoresis-time-of-flight mass spectrometry was used to quantify hydrophilic metabolites in 247 subjects with stage 0 to IV CRC or polyps, and healthy controls. The 154 identified and quantified metabolites included metabolites of glycolysis, TCA cycle, amino acids, urea cycle, and polyamine pathways. The concentrations of these metabolites gradually increased with the stage, and samples of CRC stage IV especially showed a large difference compared to other stages. Polyps and CRC also showed different concentration patterns. We also assessed the differentiation ability of these metabolites. A multiple logistic regression model using three metabolites was developed with a randomly designated training dataset and validated using the remaining data to differentiate CRC and polys from healthy controls based on a panel of urinary metabolites. These data highlight the changes in metabolites from early to late stage of CRC and also the differences between CRC and polyps.

Indexed as

MetabolomicsAgedColorectal NeoplasmsElectrophoresis, CapillaryFemaleHumansLogistic ModelsMaleMass SpectrometryMetabolomeMiddle AgedPrincipal Component Analysis

Identifiers

PMID33273632
PMCPMC7713069

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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.