Evidence map›Paper›PMID 41073134›Full record

ArticleJournal for immunotherapy of cancer2025

ALCAM-CD6 axis suppression: a key determinant of immune-mediated metastasis recurrence in stage III non-small cell lung cancer.

Shaodi Wen, Xiaoyue Du, Miaolin Zhu, Chao Huang, Zeyang Lin, Ming Li, Bowen Hu, Xin Wang, Feng Jiang, Guoren Zhou and 4 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
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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

14 authors.

Shaodi Wen *Department of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China.ORCID http://orcid.org/0000-0001-7951-0123
Xiaoyue Du *Department of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China.
Miaolin Zhu *Department of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China.
Chao HuangSchool of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China.
Zeyang LinDepartment of Anesthesiology, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Ming LiDepartment of Bioinformatics, Southern Medical University, Guangzhou, China.
Bowen HuDepartment of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China.
Xin WangDepartment of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China.
Feng JiangDepartment of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China.ORCID http://orcid.org/0000-0001-6569-5956
Guoren ZhouDepartment of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China.ORCID http://orcid.org/0000-0002-8084-2800
Wei ZhuSchool of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China.ORCID http://orcid.org/0000-0002-5237-1992
Guangchuang YuDepartment of Bioinformatics, Southern Medical University, Guangzhou, China shenbo987@njmu.edu.cn xucongharry@gmail.com gcyu1@smu.edu.cn.
Cong XuDepartment of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China shenbo987@njmu.edu.cn xucongharry@gmail.com gcyu1@smu.edu.cn.
Bo ShenDepartment of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China shenbo987@njmu.edu.cn xucongharry@gmail.com gcyu1@smu.edu.cn.ORCID http://orcid.org/0000-0001-9708-6098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastatic recurrence poses a significant challenge in cancer treatment, impacting patient survival and prognosis. Understanding the biological mechanisms behind it is essential for improving treatment strategies and patient outcomes. Lung cancer, the leading cause of cancer-related deaths, is a focus of research for treatment and prognosis. This study specifically targets stage III non-small cell lung cancer (NSCLC) patients following surgery due to their high recurrence variability.

methodsTo delve into the mechanisms of metastatic recurrence in stage III NSCLC patients, we used a comprehensive experimental approach. Long-term follow-up of postoperative patients was combined with single-cell sequencing to uncover tumor microenvironment changes. In vivo and in vitro experiments, including tissue cytometry analysis, real-time PCR, western blotting, gene silencing, cell co-culture, flow cytometry, and chromatin immunoprecipitation-quantitative PCR, were conducted to investigate ALCAM-related gene regulation. Tissue samples and clinical data were collected from stage III NSCLC patients who underwent lung cancer resection between August 2018 and July 2021.

resultsAnalysis revealed distinct epithelial gene expression patterns between recurrence and non-recurrence groups, highlighting the reduced interaction between ALCAM ligand on epithelial cells and CD6 receptor on T cells. Lower ALCAM levels intensified an immunosuppressive state, halting cell cycle progression and promoting tumor proliferation and migration, linked to metastatic recurrence. The transcription factor MYB was identified as a key ALCAM regulator, shedding light on its impact on tumor advancement. Reduced ALCAM expression correlated with poorer prognosis, offering insights into NSCLC recurrence mechanisms.

conclusionsOur study underscores the pivotal role of the ALCAM-CD6 axis in metastatic recurrence of stage III NSCLC. ALCAM regulation not only influences immune-tumor cell interactions but also drives tumor cell proliferation and migration by affecting the cell cycle. This finding presents a promising target for NSCLC treatment and aids in assessing patient prognosis effectively.

Indexed as

Antigens, CDAntigens, Differentiation, T-LymphocyteCarcinoma, Non-Small-Cell LungLung NeoplasmsNeoplasm Recurrence, LocalActivated-Leukocyte Cell Adhesion MoleculeAnimalsFemaleHumansMaleMiceMiddle AgedNeoplasm MetastasisNeoplasm StagingPrognosisTumor MicroenvironmentActivated-Leukocyte Cell Adhesion MoleculeALCAM protein, humanAntigens, CDAntigens, Differentiation, T-LymphocyteImmunosuppressionLung CancerRelapseT-Lymphocytes

Identifiers

PMID41073134
PMCPMC12516994

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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.