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A simple and scalable zebrafish model of Sonic hedgehog medulloblastoma
被引:3
|作者:
Casey, Mattie J.
[1
]
Chan, Priya P.
[2
,3
]
Li, Qing
[4
]
Zu, Ju-Fen
[1
,5
,6
]
Jette, Cicely A.
[1
]
Kohler, Missia
[7
]
Myers, Benjamin R.
[1
,5
,6
]
Stewart, Rodney A.
[1
]
机构:
[1] Univ Utah, Huntsman Canc Inst, Dept Oncol Sci, Salt Lake City, UT 84112 USA
[2] Univ Utah, Sch Med, Dept Pediat, Salt Lake City, UT 84108 USA
[3] Primary Childrens Med Ctr, Salt Lake City, UT 84113 USA
[4] Univ Utah, Huntsman Canc Inst, High Throughput Genom & Canc Bioinformat Shared Re, Salt Lake City, UT 84112 USA
[5] Univ Utah, Sch Med, Dept Biochem, Salt Lake City, UT 84112 USA
[6] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[7] Univ Utah, Sch Med, Dept Anat Pathol, Salt Lake City, UT 84112 USA
来源:
关键词:
RECEPTOR KINASE 2;
CHILDRENS ONCOLOGY;
RESISTANCE;
INHIBITOR;
TUMORS;
GENES;
STEM;
EXPRESSION;
EVOLUTION;
MUTATION;
D O I:
10.1016/j.celrep.2024.114559
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Medulloblastoma (MB) is the most common malignant brain tumor in children and is stratified into three major subgroups. The Sonic hedgehog (SHH) subgroup represents ' 30% of all MB cases and has significant survival disparity depending upon TP53 status. Here, we describe a zebrafish model of SHH MB using CRISPR to create mutant ptch1, , the primary genetic driver of human SHH MB. In these animals, tumors rapidly arise in the cerebellum and resemble human SHH MB by histology and comparative onco-genomics. Similar to human patients, MB tumors with loss of both ptch1 and tp53 have aggressive tumor histology and significantly worse survival outcomes. The simplicity and scalability of the ptch1- crispant MB model makes it highly amenable to CRISPR-based genome-editing screens to identify genes required for SHH MB tumor formation in vivo, , and here we identify the gene encoding Grk3 kinase as one such target.
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页数:22
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