Unearthing novel fusions as therapeutic targets in solid tumors using targeted RNA sequencing

被引:5
|
作者
An, Sungbin [1 ,2 ]
Koh, Hyun Hee [3 ]
Chang, Eun Sol [1 ,2 ]
Choi, Juyoung [2 ,4 ]
Song, Ji-Young [2 ]
Lee, Mi-Sook [1 ,2 ]
Choi, Yoon-La [1 ,2 ,5 ]
机构
[1] Sungkyunkwan Univ, Dept Hlth Sci & Technol, Samsung Adv Inst Hlth Sci & Technol SAIHST, Seoul, South Korea
[2] Sungkyunkwan Univ, Lab Mol Pathol & Theranot, Samsung Med Ctr, Sch Med, Seoul, South Korea
[3] Yonsei Univ, Severance Hosp, Dept Pathol, Coll Med, Seoul, South Korea
[4] Sungkyunkwan Univ, Dept Digital Hlth, Samsung Adv Inst Hlth Sci & Technol, Seoul, South Korea
[5] Sungkyunkwan Univ, Dept Pathol & Translat Genom, Samsung Med Ctr, Sch Med, Seoul, South Korea
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
基金
新加坡国家研究基金会;
关键词
fusion gene; solid tumors; next generation sequencing; diagnostics; targeted therapy; precision medicine; GENE FUSIONS; CANCER;
D O I
10.3389/fonc.2022.892918
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Detection of oncogenic fusion genes in cancers, particularly in the diagnosis of uncertain tumors, is crucial for determining effective therapeutic strategies. Although novel fusion genes have been discovered through sequencing, verifying their oncogenic potential remain difficult. Therefore, we evaluated the utility of targeted RNA sequencing in 165 tumor samples by identifying known and unknown fusions. Additionally, by applying additional criteria, we discovered eight novel fusion genes that are expected to process oncogenicity. Among the novel fusion genes, RAF1 fusion genes were detected in two cases. PTPRG-RAF1 fusion led to an increase in cell growth; while dabrafenib, a BRAF inhibitor, reduced the growth of cells expressing RAF1. This study demonstrated the utility of RNA panel sequencing as a theragnostic tool and established criteria for identifying oncogenic fusion genes during post-sequencing analysis.
引用
收藏
页数:15
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