Joint metabolomics and transcriptomics analysis systematically reveal the impact of MYCN in neuroblastoma

Bibliographic Details
Title: Joint metabolomics and transcriptomics analysis systematically reveal the impact of MYCN in neuroblastoma
Authors: Bang Du, Yingyu Zhang, Pin Zhang, Mengxin Zhang, Zhidan Yu, Lifeng Li, Ligong Hou, Qionglin Wang, Xianwei Zhang, Wancun Zhang
Source: Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Publisher Information: Nature Portfolio, 2024.
Publication Year: 2024
Collection: LCC:Medicine
LCC:Science
Subject Terms: MYCN amplification, Neuroblastoma, Metabolomics, Transcriptomics, Therapeutic target, Molecular mechanism, Medicine, Science
More Details: Abstract The limited understanding of the molecular mechanism underlying MYCN-amplified (MNA) neuroblastoma (NB) has hindered the identification of effective therapeutic targets for MNA NB, contributing to its higher mortality rate compared to MYCN non-amplified (non-MNA) NB. Therefore, a comprehensive analysis integrating metabolomics and transcriptomics was conducted to systematically investigate the MNA NB. Metabolomics analysis utilized plasma samples from 28 MNA NB patients and 68 non-MNA NB patients, while transcriptomics analysis employed tissue samples from 15 MNA NB patients and 37 non-MNA NB patients. Notably, joint metabolomics and transcriptomics analysis was performed. A total of 46 metabolites exhibited alterations, with 21 displaying elevated levels and 25 demonstrating reduced levels in MNA NB. In addition, 884 mRNAs in MNA NB showed significant changes, among which 766 mRNAs were higher and 118 mRNAs were lower. Joint-pathway analysis revealed three aberrant pathways involving glycerolipid metabolism, purine metabolism, and lysine degradation. This study highlights the substantial differences in metabolomics and transcriptomics between MNA NB and non-MNA NB, identifying three abnormal metabolic pathways that may serve as potential targets for understanding the molecular mechanisms underlying MNA NB.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2045-2322
Relation: https://doaj.org/toc/2045-2322
DOI: 10.1038/s41598-024-71211-x
Access URL: https://doaj.org/article/83767d9192974dd7bff3ebb90542f970
Accession Number: edsdoj.83767d9192974dd7bff3ebb90542f970
Database: Directory of Open Access Journals
Full text is not displayed to guests.
More Details
ISSN:20452322
DOI:10.1038/s41598-024-71211-x
Published in:Scientific Reports
Language:English