DNA损伤
聚ADP核糖聚合酶
神经母细胞瘤
灵敏度(控制系统)
DNA
癌症研究
生物
遗传学
医学
聚合酶
细胞培养
电子工程
工程类
作者
Madeline N. Hayes,Sarah Cohen‐Gogo,Lynn Kee,Xueting Xiong,A. H. Weiss,Mehdi Layeghifard,Yagnesh Ladumor,Ivette Valencia-Sama,Anisha Rajaselvam,David R. Kaplan,Anita Villani,Adam Shlien,Daniel A. Morgenstern,Meredith S. Irwin
出处
期刊:Cell Reports
[Elsevier]
日期:2025-04-01
卷期号:44 (4): 115537-115537
标识
DOI:10.1016/j.celrep.2025.115537
摘要
Sequencing of neuroblastoma (NB) tumors has revealed genetic alterations in genes involved in DNA damage response (DDR) pathways. However, roles for specific alterations of DDR genes in pediatric solid tumors remain poorly understood. To address this, mutations in the DDR pathway including Brca2, Atm, and Palb2 were incorporated into an established zebrafish MYCN transgenic model (Tg(dbh:EGFP-MYCN)). These mutations enhance NB formation and metastasis and result in upregulation of cell-cycle checkpoint and DNA damage repair signatures, revealing molecular vulnerabilities in DDR-deficient NB. DDR gene knockdown in zebrafish and human NB cells increases sensitivity to the poly(ADP-ribose) polymerase (PARP) inhibitor olaparib, and this effect is enhanced by inhibition of the ataxia telangiectasia and rad3-related (ATR) kinase. This work provides in vivo evidence demonstrating that alterations in certain DDR-pathway genes promote aggressive NB and supports combination PARP + ATR inhibitor therapy for NB patients with tumors harboring specific genetic alterations in DDR.
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