A pediatric brain tumor atlas of genes deregulated by somatic genomic rearrangement
Yiqun Zhang,
Fengju Chen,
Lawrence A. Donehower,
Michael E. Scheurer and
Chad J. Creighton ()
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Yiqun Zhang: Baylor College of Medicine
Fengju Chen: Baylor College of Medicine
Lawrence A. Donehower: Baylor College of Medicine
Michael E. Scheurer: Baylor College of Medicine
Chad J. Creighton: Baylor College of Medicine
Nature Communications, 2021, vol. 12, issue 1, 1-17
Abstract:
Abstract The global impact of somatic structural variants (SSVs) on gene expression in pediatric brain tumors has not been thoroughly characterised. Here, using whole-genome and RNA sequencing from 854 tumors of more than 30 different types from the Children’s Brain Tumor Tissue Consortium, we report the altered expression of hundreds of genes in association with the presence of nearby SSV breakpoints. SSV-mediated expression changes involve gene fusions, altered cis-regulation, or gene disruption. SSVs considerably extend the numbers of patients with tumors somatically altered for critical pathways, including receptor tyrosine kinases (KRAS, MET, EGFR, NF1), Rb pathway (CDK4), TERT, MYC family (MYC, MYCN, MYB), and HIPPO (NF2). Compared to initial tumors, progressive or recurrent tumors involve a distinct set of SSV-gene associations. High overall SSV burden associates with TP53 mutations, histone H3.3 gene H3F3C mutations, and the transcription of DNA damage response genes. Compared to adult cancers, pediatric brain tumors would involve a different set of genes with SSV-altered cis-regulation. Our comprehensive and pan-histology genomic analyses reveal SSVs to play a major role in shaping the transcriptome of pediatric brain tumors.
Date: 2021
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21081-y
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DOI: 10.1038/s41467-021-21081-y
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