Evidence map›Paper›PMID 40610605›Full record

ArticleScientific reports2025

Exploring the impact of neutrophils on lung adenocarcinoma using Mendelian randomization and transcriptomic study.

Xiang Xiao, Xuan-Yu Wu, Jing-Qi Zhang, Wen-Yuan Li, Feng-Ming You, Jing Guo

Abstract read
In one paragraph

Article in Scientific reports, 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

6 authors.

Xiang Xiao *Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu University of Traditional Chinese Medicine, Shi-er-qiao Road, Chengdu City, Sichuan Province, China.
Xuan-Yu Wu *Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu University of Traditional Chinese Medicine, Shi-er-qiao Road, Chengdu City, Sichuan Province, China.
Jing-Qi ZhangHospital of Chengdu University of Traditional Chinese Medicine, Chengdu University of Traditional Chinese Medicine, Shi-er-qiao Road, Chengdu City, Sichuan Province, China.
Wen-Yuan LiHospital of Chengdu University of Traditional Chinese Medicine, Chengdu University of Traditional Chinese Medicine, Shi-er-qiao Road, Chengdu City, Sichuan Province, China.
Feng-Ming YouHospital of Chengdu University of Traditional Chinese Medicine, Chengdu University of Traditional Chinese Medicine, Shi-er-qiao Road, Chengdu City, Sichuan Province, China. youfengming@cdutcm.edu.cn.
Jing GuoHospital of Chengdu University of Traditional Chinese Medicine, Chengdu University of Traditional Chinese Medicine, Shi-er-qiao Road, Chengdu City, Sichuan Province, China. guojing19910307@sina.com.

Funding

China Postdoctoral Science Foundation 2022MD723715National Natural Science Foundation of China 82305188Natural Science Foundation of Sichuan Science and Technology Department 23NSFSC6246
6 · The paper itself

Abstract

Tumor immune microenvironment plays a crucial role in determining the prognosis of lung adenocarcinoma (LUAD), with the interaction of immune cells within this microenvironment contributing to a poorer prognosis. We sought to investigate the causal relationship and underlying biological mechanisms between immune cell characteristics and LUAD to offer new insights for enhancing treatment strategies. We evaluated the association between immune cell characteristics and LUAD using Mendelian randomization (MR) analysis based on genome-wide association studies summary statistics. Sensitivity analysis was performed to verify the robustness of MR results. Immune cell infiltration analysis and machine learning on bulk RNA-sequencing data were conducted to further identify immune cells associated with LUAD. Prognostic genes of LUAD were identified using single-cell RNA-sequencing data and high dimensional weighted gene co-expression network analysis. MR analysis identified three immune cell characteristics associated with LUAD, including CCR2 on granulocyte, CD25 on CD45RA + CD4 not Treg, and plasmacytoid dendritic cell, and sensitivity analysis confirmed the robustness of the associations. Machine learning identified neutrophils, hematopoietic stem cells, B cells, and myeloid progenitor cells as key immune cell characteristics related to LUAD. Neutrophil was identified as the target cell of LUAD based on the MR analysis and machine learning. Subcequently, single-cell RNA-sequencing mapped the immune microenvironment of LUAD and identified down-regulated neutrophil. In addition, robust neutrophil-macrophage communication in LUAD was revealed using the CellChat package. Finally, nine neutrophil-related prognostic genes of LUAD were identified, three of which potentially regulated neutrophil-macrophage communication. This study showed a significant correlation between neutrophil and LUAD, particularly highlighting the neutrophil-macrophage communication. This finding may enhance our comprehension of LUAD immune microenvironment and hopefully promote the discovery of new immunotherapeutic targets for LUAD and the development of related drugs.

Indexed as

Adenocarcinoma of LungLung NeoplasmsNeutrophilsTranscriptomeGene Expression ProfilingGene Expression Regulation, NeoplasticGenome-Wide Association StudyHumansMachine LearningMendelian Randomization AnalysisPrognosisSingle-Cell AnalysisTumor MicroenvironmentBulk RNA-sequencinghdWGCNAImmune cell characteristicsLung adenocarcinomaMendelian randomizationNeutrophilSingle-cell RNA-sequencing

Identifiers

PMID40610605
PMCPMC12226722

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