Evidence map›Paper›PMID 36264865›Full record

ArticlePloS one2022

Molecular and clinicopathological differences between depressed and protruded T2 colorectal cancer.

Kenichi Mochizuki, Shin-Ei Kudo, Kazuki Kato, Koki Kudo, Yushi Ogawa, Yuta Kouyama, Yuki Takashina, Katsuro Ichimasa, Taro Tobo, Takeo Toshima and 7 more

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

17 authors.

Kenichi MochizukiDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.ORCID 0000-0002-3196-5679
Shin-Ei KudoDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Kazuki KatoDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Koki KudoDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Yushi OgawaDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Yuta KouyamaDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Yuki TakashinaDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Katsuro IchimasaDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Taro ToboDepartment of Clinical Laboratory, Kyushu University Beppu Hospital, Beppu, Japan.
Takeo ToshimaDepartment of Surgery, Kyushu University Beppu Hospital, Beppu, Japan.ORCID 0000-0003-4019-8288
Yuichi HisamatsuDepartment of Surgery, Kyushu University Beppu Hospital, Beppu, Japan.
Yusuke YonemuraDepartment of Surgery, Kyushu University Beppu Hospital, Beppu, Japan.
Takaaki MasudaDepartment of Surgery, Kyushu University Beppu Hospital, Beppu, Japan.
Hideyuki MiyachiDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Fumio IshidaDigestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Tetsuo NemotoDepartment of Diagnostic Pathology, School of Medicine, Showa University, Yokohama Northern Hospital, Kanagawa, Japan.
Koshi MimoriDepartment of Surgery, Kyushu University Beppu Hospital, Beppu, Japan.ORCID 0000-0003-3897-9974

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) can be classified into four consensus molecular subtypes (CMS) according to genomic aberrations and gene expression profiles. CMS is expected to be useful in predicting prognosis and selecting chemotherapy regimens. However, there are still no reports on the relationship between the morphology and CMS.

methodsThis retrospective study included 55 subjects with T2 CRC undergoing surgical resection, of whom 30 had the depressed type and 25 the protruded type. In the classification of the CMS, we first defined cases with deficient mismatch repair as CMS1. And then, CMS2/3 and CMS4 were classified using an online classifier developed by Trinh et al. The staining intensity of CDX2, HTR2B, FRMD6, ZEB1, and KER and the percentage contents of CDX2, FRMD6, and KER are input into the classifier to obtain automatic output classifying the specimen as CMS2/3 or CMS4.

resultsAccording to the results yielded by the online classifier, of the 30 depressed-type cases, 15 (50%) were classified as CMS2/3 and 15 (50%) as CMS4. Of the 25 protruded-type cases, 3 (12%) were classified as CMS1 and 22 (88%) as CMS2/3. All of the T2 CRCs classified as CMS4 were depressed CRCs. More malignant pathological findings such as lymphatic invasion were associated with the depressed rather than protruded T2 CRC cases.

conclusionsDepressed-type T2 CRC had a significant association with CMS4, showing more malignant pathological findings such as lymphatic invasion than the protruded-type, which could explain the reported association between CMS4 CRC and poor prognosis.

Indexed as

Colorectal NeoplasmsBiomarkers, TumorHumansPrognosisRetrospective StudiesTranscriptomeBiomarkers, Tumor

Identifiers

PMID36264865
PMCPMC9584453

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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.