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Pan-Cancer Analysis Reveals Recurrent BCAR4 Gene Fusions across Solid Tumors
被引:6
|作者:
Nickless, Andrew
[1
]
Zhang, Jin
[2
,3
,4
]
Othoum, Ghofran
[1
]
Webster, Jace
[1
]
Inkman, Matthew J.
[2
]
Coonrod, Emily
[1
]
Fontes, Sherron
[1
]
Rozycki, Emily B.
[1
]
Maher, Christopher A.
[1
,3
,5
,6
]
White, Nicole M.
[1
,3
,6
]
机构:
[1] Washington Univ, Siteman Canc Ctr, Dept Med, Div Oncol,Sch Med, St Louis, MO USA
[2] Washington Univ, Dept Radiat Oncol, Sch Med, St Louis, MO USA
[3] Washington Univ, Siteman Canc Ctr, Sch Med, St Louis, MO USA
[4] Washington Univ, Inst Informat, Sch Med, St Louis, MO USA
[5] Washington Univ, Dept Biomed Engn, Sch Med, St Louis, MO USA
[6] Washington Univ, 660 S Euclid Ave, Campus Box 8056, St Louis, MO 63110 USA
关键词:
STATISTICAL-MODEL;
PROTEIN;
DISCOVERY;
DATABASE;
GENOME;
D O I:
10.1158/1541-7786.MCR-21-0775
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Chromosomal rearrangements often result in active regulatory regions juxtaposed upstream of an oncogene to generate an expressed gene fusion. Repeated activation of a common downstream partner–with differing upstream regions across a patient cohort–suggests a conserved oncogenic role. Analysis of 9,638 patients across 32 solid tumor types revealed an annotated long noncoding RNA (lncRNA), Breast Cancer Anti-Estrogen Resistance 4 (BCAR4), was the most prevalent, uncharacterized, downstream gene fusion partner occurring in 11 cancers. Its oncogenic role was confirmed using multiple cell lines with endogenous BCAR4 gene fusions. Furthermore, overexpressing clinically prevalent BCAR4 gene fusions in untransformed cell lines was sufficient to induce an oncogenic phenotype. We show that the minimum common region to all gene fusions harbors an open reading frame that is necessary to drive proliferation. ©2022 The Authors; Published by the American Association for Cancer Research.
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页码:1481 / 1488
页数:8
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