Evidence map›Paper›PMID 41640009›Full record

ArticleImmunity, inflammation and disease2026

Integrative Omics Analysis Reveals the Potential Value of CEACAM6 in Pan-Gastrointestinal Cancers.

Liying Jin, Changjuan Tao, Zhiyong Pan, Peng Zhang

Abstract read
In one paragraph

Article in Immunity, inflammation and disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Liying JinDepartment of Gastroenterology, Xianju People's Hospital, Taizhou, China.
Changjuan TaoDepartment of Radiation Oncology, The Cancer Hospital of the University of Chinese Academy of Sciences, Zhejiang Cancer Hospital, Hangzhou, China.
Zhiyong PanDepartment of Neurology, Yueyang People's Hospital, Yueyang, China.
Peng ZhangDepartment of Medical Oncology, Zhejiang Provincial People's Hospital, Hangzhou, China.ORCID https://orcid.org/0000-0001-9637-2842

Funding

Medical Science and Technology Project of Zhejiang Province 2024KY047Natural Science Foundation of Zhejiang Province Q24H160113
6 · The paper itself

Abstract

objectiveCarcinoembryonic antigen cell adhesion molecule 6 (CEACAM6) is known as a cell adhesion receptor which could regulate proliferation and other signaling in cancer. The role of CEACAM6 in pan-gastrointestinal cancers remains largely uncharacterized. This study employed multi-omics bioinformatics to investigate the expression distribution, prognostic value, and immune function of CEACAM6 in these malignancies.

methodsUtilizing multi-omics data from The Cancer Genome Atlas (TCGA), cBioPortal, GDSC2, TIMER2.0, and TISCH databases, we assessed the CEACAM6 expression and prognostic value across pan-gastrointestinal cancers. Additionally, the potential role of CEACAM6 in the tumor immune microenvironment was explored using multi-omics data, including spatial transcriptomics data.

resultsBased on TCGA data, CEACAM6 was found to be overexpressed in pan-gastrointestinal cancers. The CEACAM6 somatic copy number alterations, DNA methylation and mutation sites were identified as potential contributors to abnormal CEACAM6 expression. The CEACAM6 expression was significantly negatively associated with the abundance of CD4 + Th1 cells across pan-gastrointestinal cancers. Furthermore, spatial transcriptomics data revealed that CEACAM6 expression was significant positively associated with malignant cells, while there was a negative correlation was observed with between CEACAM6 expression and plasma cells.

conclusionCEACAM6 exhibits high diagnostic accuracy and tumor-specific overexpression in pan-gastrointestinal cancers. CEACAM6 could promote angiogenesis/metastasis and suppress anti-tumor immunity. Spatially localized in tumors with immune cell exclusion, CEACAM6 correlates with poor survival and immune-excluded subtypes, positioning it as a therapeutic target in precision immunotherapy for pan-gastrointestinal cancers.

Indexed as

Antigens, CDBiomarkers, TumorCell Adhesion MoleculesGastrointestinal NeoplasmsComputational BiologyDNA Copy Number VariationsDNA MethylationGene Expression ProfilingGene Expression Regulation, NeoplasticGPI-Linked ProteinsHumansMultiomicsPrognosisSpatial TranscriptomicsTumor MicroenvironmentAntigens, CDBiomarkers, TumorCEACAM6 protein, humanCell Adhesion MoleculesGPI-Linked ProteinsCEACAM6pan‐gastrointestinal cancersprognosistumor immune microenvironment

Identifiers

PMID41640009
PMCPMC12872969

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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.