Evidence map›Paper›PMID 33005848›Full record

ReviewAnnals of gastroenterological surgery2020

Investigation of colorectal cancer in accordance with consensus molecular subtype classification.

Hiroshi Sawayama, Yuji Miyamoto, Katsuhiro Ogawa, Naoya Yoshida, Hideo Baba

Abstract readReview
In one paragraph

Review in Annals of gastroenterological surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Article
  2. Article
  3. Advances in Colorectal Cancer Cell Biology and Clonal Evolution.International journal of molecular sciences · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Observational
  8. Review
  9. Article
  10. Article
  11. Identification of a Novel 4-gene Prognostic Model Related to Neutrophil Extracellular Traps for Colorectal Cancer.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Controversial role of γδ T cells in colorectal cancer.American journal of cancer research · 2024
    Review
  20. 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

5 authors.

Hiroshi SawayamaDepartment of Gastroenterological Surgery Graduate School of Medical Sciences Kumamoto University Honjo Japan.ORCID https://orcid.org/0000-0002-0082-7601
Yuji MiyamotoDepartment of Gastroenterological Surgery Graduate School of Medical Sciences Kumamoto University Honjo Japan.
Katsuhiro OgawaDepartment of Gastroenterological Surgery Graduate School of Medical Sciences Kumamoto University Honjo Japan.
Naoya YoshidaDepartment of Gastroenterological Surgery Graduate School of Medical Sciences Kumamoto University Honjo Japan.ORCID https://orcid.org/0000-0002-8447-5278
Hideo BabaDepartment of Gastroenterological Surgery Graduate School of Medical Sciences Kumamoto University Honjo Japan.ORCID https://orcid.org/0000-0002-3474-2550

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The classification of colorectal cancer (CRC) plays a pivotal role in predicting a patient's prognosis and determining treatment strategies. The consensus molecular subtype (CMS) classification system was constructed by analyzing genetic information from 18 CRC data sets, containing 4151 CRC samples. CRC was classified into four subtypes with distinct molecular and biological characteristics: CMS1 (microsatellite instability immune), CMS2 (canonical), CMS3 (metabolic), and CMS4 (mesenchymal). Since their designation in 2015, these classifications have been applied to basic and translational research of CRC, with the hope that understanding these subsets will influence a clinician's approach to therapeutic treatment and improve clinical outcomes. We reviewed CRC investigations in accordance with CMSs published in the last 5 years to further explore the clinical significance of these subtypes and identify underlying trends that may direct relevant future research. We determined that CMSs linked common features of CRC cell lines and PDX models in various studies. Furthermore, associations between prognosis and clinicopathological findings, including pathological grade and the stage of carcinogenesis, tumor budding, and tumor location, were correlated with CMS classification. Novel prognostic factors were identified, and the relationship between chemotherapeutic drug resistance and CMS has been fortified by our compilation of research; thus, indicating that this review provides advanced insight into clinical questions and treatment strategies for CRC.

Indexed as

colorectal cancerconsensus molecular subtypeprognostic marker

Identifiers

PMID33005848
PMCPMC7511559

What Socratic holds

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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 Socratic graph.