Evidence map›Paper›PMID 42269080›Full record

ArticlePathology international2026

Low Expression of Cell Adhesion Molecule 1 in Resected Gastroenteropancreatic Neuroendocrine Tumors: Relationship With Lymph Node and Distant Metastasis.

Ken Miyabe, Michinobu Umakoshi, Yukitsugu Kudo-Asabe, Kei Koyama, Takahiro Ishinari, Ayana Takahashi, Hikaru Tsukita, Yukinobu Ito, Makoto Yoshida, Masato Takahashi and 5 more

Abstract read
In one paragraph

Article in Pathology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Ken MiyabeDepartment of Quantitative Pathology, Akita University Graduate School of Medicine, Akita, Japan.ORCID https://orcid.org/0009-0006-0105-7027
Michinobu UmakoshiDepartment of Quantitative Pathology, Akita University Graduate School of Medicine, Akita, Japan.ORCID https://orcid.org/0000-0001-7013-0503
Yukitsugu Kudo-AsabeDepartment of Quantitative Pathology, Akita University Graduate School of Medicine, Akita, Japan.
Kei KoyamaDepartment of Quantitative Pathology, Akita University Graduate School of Medicine, Akita, Japan.
Takahiro IshinariDepartment of Quantitative Pathology, Akita University Graduate School of Medicine, Akita, Japan.
Ayana TakahashiDepartment of Quantitative Pathology, Akita University Graduate School of Medicine, Akita, Japan.
Hikaru TsukitaDepartment of Quantitative Pathology, Akita University Graduate School of Medicine, Akita, Japan.
Yukinobu ItoDepartment of Molecular and Cellular Pathology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.ORCID https://orcid.org/0000-0002-1774-1169
Makoto YoshidaCourse of Occupational Therapy, Department of Health Sciences, Akita Uversity Graduate School of Health Sciences, Akita, Japan.
Masato TakahashiDepartment of Pathology, Akita Kosei Medical Center, Akita, Japan.
Tatsuo SugiyamaDepartment of Pathology, Akita Kosei Medical Center, Akita, Japan.
Masato SageshimaDepartment of Pathology, Akita City Hospital, Akita, Japan.
Hiroshi NanjoDivision of Clinical Pathology, Akita University Hospital, Akita, Japan.
Yoshinori MurakamiDivision of Molecular Pathology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-2826-4396
Akiteru GotoDepartment of Quantitative Pathology, Akita University Graduate School of Medicine, Akita, Japan.ORCID https://orcid.org/0000-0001-8776-9004

Funding

Japan Society for the Promotion of Science 19K07454Japan Society for the Promotion of Science 21K15380Japan Society for the Promotion of Science 24K10104
6 · The paper itself

Abstract

Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are clinically heterogeneous, making prediction of metastatic behavior challenging. This study examined Cell Adhesion Molecule 1 (CADM1) and the differentially expressed in adenocarcinoma of the lung-1 expression in 75 resected GEP-NETs and evaluated their associations with clinicopathological features, tumor grade, and established adhesion- or prognosis-related markers, including E-cadherin (ECAD), CD56, progesterone receptor (PgR), and cytokeratin 19 (CK19). CADM1 promoter methylation was assessed using methylation-specific PCR, and the miR-214 and miR-375 expressions were analyzed by quantitative real-time PCR. The expression of CADM1 was significantly lower in tumors with lymph node and/or distant metastasis (p = 0.01), and a low CADM1 expression was independently associated with metastatic disease (p = 0.0004; OR = 4.63). Additionally, low PgR (p = 0.014; OR = 4.13) and a high CK19 (p = 0.0002; OR = 4.83) expression, as reported previously, were linked to poor outcomes. In contrast, neither ECAD nor CD56 showed any notable associations with aggressive features in a univariable assessment. No significant relationship was observed between CADM1 promoter methylation and the CADM1 expression. These findings suggest that a reduced CADM1 expression may be associated with lymph node and distant metastasis in GEP-NETs and could be a potential prognostic marker.

Indexed as

Biomarkers, TumorCell Adhesion Molecule-1Intestinal NeoplasmsNeuroendocrine TumorsPancreatic NeoplasmsStomach NeoplasmsAdultAgedDNA MethylationFemaleHumansLymphatic MetastasisMaleMiddle AgedPrognosisBiomarkers, TumorCADM1 protein, humanCell Adhesion Molecule-1cell adhesion molecule 1 (CADM1)differentially expressed in adenocarcinoma of the lung‐1 (DAL‐1)gastroenteropancreatic neuroendocrine tumors (GEP‐NETs)

Identifiers

PMID42269080
PMCPMC13252909

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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.