Evidence map›Paper›PMID 42050733›Full record

ArticleHuman genomics2026

Comprehensive transcriptomics and proteome analysis to identify prognostic risk factors for MYCN non-amplified high-risk neuroblastoma.

Shan Liu, Zhihong Wang, Jianzhen Shen, Lizhi Li, Yaobin Lin

Abstract read
In one paragraph

Article in Human genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Shan LiuDepartment of Hematology-Oncology, Fujian Children's Hospital, College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, Fujian, China.
Zhihong WangDepartment of Hematology, Fuzhou University Affiliated Provincial Hospital, Fujian Provincial Hospital, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, Fujian, China.
Jianzhen ShenDepartment of Hematology, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Lizhi LiFuzhou University Affiliated Provincial Hospital, Fujian Provincial Hospital, Fuzhou, Fuzhou, Fujian, China.
Yaobin LinDepartment of Radiation Oncology, Clinical Research Center for Radiology and Radiotherapy of Fujian Province (Digestive, Hematological and Breast Malignancies), Fujian Medical University Union Hospital, Fujian Key Laboratory of Intelligent Imaging and Precision Radiotherapy for Tumors (Fujian Medical University), Fuzhou, 350000, Fujian, China. yaobinlin@fjmu.edu.cn.

Funding

Fujian Provincial Natural Science Foundation of China 2024J0112Joint Funds for the Innovation of Science and Technology, Fujian Province 2024Y9554Xiamen Medical College School-Hospital Joint Funding Project K2023-03
6 · The paper itself

Abstract

backgroundMYCN non-amplified (MYCN-NA) neuroblastoma (NB) demonstrates considerable heterogeneity in both biological and clinical aspects, and its molecular and biological characteristics remain inadequately defined.

methodsA comprehensive multi-omics analysis was performed on transcriptome and proteome data from 20 MYCN-NA NB tissues, including 11 low- and intermediate-risk neuroblastoma (LIR-NB) cases and 9 high-risk neuroblastoma (HR-NB) cases. Additionally, the expression levels and survival prognostic significance of key candidate genes were systematically assessed using public datasets (GSE85047 and TARGET-NB).

resultsTranscriptomic analysis revealed 1,955 differentially expressed genes (DEGs), with 899 upregulated and 1,056 downregulated in HR-NB (P < 0.05, |log

conclusionMYCN-NA HR-NB demonstrates metabolic reprogramming characterized by disorders in glucose and lipid metabolism. Notably, the elevated expression of INPP5F and LGI3 is linked to improved overall survival and may serve as potential therapeutic targets.

Indexed as

NeuroblastomaN-Myc Proto-Oncogene ProteinProteomeTranscriptomeBiomarkers, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMultiomicsPrognosisProteomicsRisk FactorsBiomarkers, TumorMYCN protein, humanN-Myc Proto-Oncogene ProteinProteomeHigh-risk neuroblastomaMolecular targetsMYCN-NAProteomicsTranscriptomics

Identifiers

PMID42050733
PMCPMC13267346

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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.