Evidence map›Paper›PMID 41993132›Full record

ArticleHuman mutation2026

Targeting LY6E Inhibits Neuroblastoma Progression and Suppresses M2 Macrophage Polarization.

Lijuan Li, Yu Zeng, Qinfen Zhang, Gaojian Zhuang, Yu Liu, Xuan Wang, Yuqi Wang

Abstract read
In one paragraph

Article in Human mutation, 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

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

7 authors.

Lijuan LiHealth Management Center, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China, tijmu.edu.cn.
Yu ZengDepartment of Immunology, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Key Laboratory of Cancer Immunology and Biotherapy, State Key Laboratory of Druggability Evaluation and Systematic Translational Medicine, Tianjin, China, tijmu.edu.cn.ORCID https://orcid.org/0000-0003-2808-0711
Qinfen ZhangDepartment of Immunology, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Key Laboratory of Cancer Immunology and Biotherapy, State Key Laboratory of Druggability Evaluation and Systematic Translational Medicine, Tianjin, China, tijmu.edu.cn.
Gaojian ZhuangDepartment of Thyroid and Breast Surgery, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital) of Guangzhou Medical University, Qingyuan, Guangdong, China.
Yu LiuThe Third Department of Breast Cancer, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China, tijmu.edu.cn.
Xuan WangDepartment of Phase I clinical trial, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China, tijmu.edu.cn.ORCID https://orcid.org/0009-0008-1130-8373
Yuqi WangHealth Management Center, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China, tijmu.edu.cn.ORCID https://orcid.org/0000-0002-2150-4617

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuroblastoma is a pediatric malignancy characterized by significant clinical heterogeneity. Although MYCN amplification is a well-established marker of high-risk disease, its interplay with the tumor immune microenvironment-particularly tumor-associated macrophages (TAMs)-remains poorly understood. In this study, we developed an integrated gene signature incorporating genes associated with both MYCN amplification status and TAM infiltration, leading to the identification of 16 differentially expressed genes implicated in both biological processes. Six of these genes (CMBL, LY6E, KLRB1, CTSH, CD3D, and PTGDS) were utilized to construct a risk-scoring model that effectively stratified neuroblastoma patients into high- and low-risk groups with significantly distinct clinical outcomes (

Indexed as

Antigens, LyMacrophagesNeuroblastomaTumor-Associated MacrophagesAnimalsCell Line, TumorDisease ProgressionGene Expression ProfilingGene Expression Regulation, NeoplasticHumansN-Myc Proto-Oncogene ProteinPrognosisTumor MicroenvironmentAntigens, LyN-Myc Proto-Oncogene ProteinLY6Eneuroblastomaprognosisrisk score modeltumor-associated macrophages (TAMs)

Identifiers

PMID41993132
PMCPMC13080879

What OpenQuestion holds

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Registered trials

None linked

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.