Literature DB >> 33681213

Genomic and Transcriptomic Analyses Reveals ZNF124 as a Critical Regulator in Highly Aggressive Medulloblastomas.

Zaili Luo1, Xinran Dong1, Jianzhong Yu1, Yong Xia2, Kalen P Berry3, Rohit Rao3, Lingli Xu1, Ping Xue1, Tong Chen1, Yifeng Lin1, Jiyang Yu4, Guoying Huang1, Hao Li1, Wenhao Zhou1, Q Richard Lu3.   

Abstract

Medulloblastoma (MB) is the most common malignant pediatric brain tumor, however, the mechanisms underlying tumorigenesis in different MB subgroups remain incompletely understood. Although previous studies of MB predisposition have been conducted in tertiary referral centers primarily in Caucasian cohorts, it is not unclear clear whether there exist population-specific genetic alterations in MBs. In this study, we investigated the contribution of genomic and transcriptomic alterations to the risk of malignant MB in the Chinese population (designated as the Asian cohort). We analyze the genomic and transcriptomic alterations of the Asian MB cohort by using a combination of whole-exome sequencing (WES) and RNA-deep-sequencing. In addition, we integrate publicly available data with the Asian MB cohort and identify a subset of potential MB-driving genes specifically enriched in each of the MB subgroups. We further characterize a newly identified group-3-enriched transcriptional regulator, ZNF124, and demonstrate that ZNF124 is critical for the growth of the most aggressive group-3 MB cells. Together, our analyses indicate conserved yet distinct genetic alterations and gene expression patterns of MBs between different ethnic groups. Our studies further provide an important resource for identifying potential tumor-driving factors in MBs, enhancing our understanding of the disease process for developing ethnically targeted therapies in patients with MB.
Copyright © 2021 Luo, Dong, Yu, Xia, Berry, Rao, Xu, Xue, Chen, Lin, Yu, Huang, Li, Zhou and Lu.

Entities:  

Keywords:  Asian cohort; RNA-seq; ZNF124; medulloblastoma; racial and ethnic disparities; subgroup-specific regulator; whole exome sequencing

Year:  2021        PMID: 33681213      PMCID: PMC7930499          DOI: 10.3389/fcell.2021.634056

Source DB:  PubMed          Journal:  Front Cell Dev Biol        ISSN: 2296-634X


  48 in total

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