Evidence map›Paper›PMID 40042109›Full record

ArticleCancer medicine2025

Melanoma Cell Adhesion Molecule Plays a Pivotal Role in Proliferation, Migration, Tumor Immune Microenvironment, and Immunotherapy in Colorectal Cancer.

Jingkai Zhou, Jing Liu, Yali Yu, Haihang Nie, Yuntian Hong, Yumei Ning, Chao Yang, Jun Lai, Haizhou Wang, Xuelian Tang and 2 more

Abstract read
In one paragraph

Article in Cancer medicine, 2025. 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

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

1 citing paper in PubMed.

  1. 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

12 authors.

Jingkai ZhouDepartment of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Jing LiuEmergency Medicine Center, Zhongnan Hospital of Wuhan University, Wuhan, China.
Yali YuDepartment of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Haihang NieDepartment of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Yuntian HongDepartment of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Yumei NingDepartment of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Chao YangDepartment of Radiology, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang, China.
Jun LaiThe Infirmary of Hangzhou Power Supply Company of State Grid, Zhejiang Electric Power Co., Ltd, Hangzhou, China.
Haizhou WangDepartment of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Xuelian TangDepartment of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Fan WangDepartment of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China.ORCID https://orcid.org/0009-0005-1207-7325
Qiu ZhaoDepartment of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China.ORCID https://orcid.org/0000-0002-3230-6077

Funding

Hubei Province health and family planning scientific research project WJ2023M065Key Project of Discipline and Platform Construction of Zhongnan Hospital of Wuhan University PTXM2023012National Key Clinical Specialty Construction Project GJLCZD2023002National Natural Science Foundation of China 82203338Special Project of knowledge Innovation of Wuhan Science and Technology Bureau (Dawning project) KYXM2022007the National Natural Science Foundation of China 82403279The Science and Technology Innovation Cultivation Fund of Zhongnan Hospital, Wuhan University CXPY2024002
6 · The paper itself

Abstract

introductionMCAM, alternatively referred to as CD146, is an integral membrane glycoprotein belonging to the immunoglobulin superfamily. However, its importance in the tumorigenesis of colorectal cancer is still partially understood. Therefore, this study was designed to investigate the significance of MCAM in colorectal cancer.

methodsMCAM expression was analyzed by TCGA and GEO databases. qRT-PCR and IHC analysis were conducted to validate MCAM expression in patient tissues. The tumor-inhibiting ability of MCAM was further assessed by CCK-8 assay, colony formation assay, and wound-healing assay. qRT-PCR and WB analysis were conducted to evaluate the expression of EMT markers and MMP2/9. qRT-PCR analysis was utilized to detect the polarization status of macrophages. Kaplan-Meier curve, univariate, and multivariate cox analyses were employed to verify the ability of MCAM in prognosis prediction. TIDE scores were used to assess the impact of MCAM on immunotherapy.

resultsThe expression of MCAM was significantly downregulated in CRC, and low MCAM expression revealed poor prognosis in CRC patients. Moreover, MCAM overexpression inhibited the proliferation, migration, and invasive ability of CRC cells. Additionally, MCAM overexpression suppressed N-cadherin and MMP2/9 expression. Furthermore, MCAM impacted M1 macrophage polarization. MCAM is an independent predictor of CRC patient prognosis through Cox regression analysis. Lastly, TIDE score analysis indicated that elevated expression of MCAM increased immunotherapy efficacy.

conclusionThe findings of this research suggest that MCAM impacts M1 macrophage polarization and enhances immunotherapy efficacy, underscoring its potential as a therapeutic target for colorectal cancer.

Indexed as

CD146 AntigenColorectal NeoplasmsTumor MicroenvironmentBiomarkers, TumorCell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansImmunotherapyMacrophagesMaleMiddle AgedPrognosisBiomarkers, TumorCD146 AntigenMCAM protein, humancolorectal cancerEMTmacrophagesMCAMTIDE

Identifiers

PMID40042109
PMCPMC11880918

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LicenceCC BY
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Registered trials

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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.