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Identification of recurrent FHL2-GLI2 oncogenic fusion in sclerosing stromal tumors of the ovary

机译:卵巢硬化基质肿瘤中的复发性FHL2-GLI2致癌融合的鉴定

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Sclerosing stromal tumor (SST) of the ovary is a rare type of sex cord-stromal tumor (SCST), whose genetic underpinning is currently unknown. Here, using whole-exome, targeted capture and RNA-sequencing, we report recurrent FHL2-GLI2 fusion genes in 65% (17/26) of SSTs and other GLI2 rearrangements in additional 15% (4/26) SSTs, none of which are detected in other types of SCSTs (n?=?48) or common cancer types (n?=?9,950). The FHL2-GLI2 fusions result in transcriptomic activation of the Sonic Hedgehog (SHH) pathway in SSTs. Expression of the FHL2-GLI2 fusion in vitro leads to the acquisition of phenotypic characteristics of SSTs, increased proliferation, migration and colony formation, and SHH pathway activation. Targeted inhibition of the SHH pathway results in reversal of these oncogenic properties, indicating its role in the pathogenesis of SSTs. Our results demonstrate that the FHL2-GLI2 fusion is likely the oncogenic driver of SSTs, defining a genotypic-phenotypic correlation in ovarian neoplasms.
机译:卵巢的硬化基质肿瘤(SST)是一种罕见的性脐带 - 基质肿瘤(SCST),其遗传内宁目前未知。在这里,使用全极端,靶向捕获和RNA测序,我们在SSTS的65%(17/26)和其他GLI2重排中报告了65%(17/26)的再现15%(4/26)SST,其中任何一个以其他类型的SCST(n?=α48)或常见的癌症类型(n?= 9,950)中检测到。 FHL2-GLI2融合导致SSTS中SONON HEDGEHOG(SHH)途径的转录组激活。体外FHL2-GLI2融合的表达导致采集SSTS的表型特征,增加增殖,迁移和菌落形成,以及SHH途径激活。靶向抑制SHH途径导致这些致癌性质的逆转,表明其在SSTS发病机制中的作用。我们的结果表明,FHL2-GLI2融合可能是SST的致癌驱动器,定义卵巢肿瘤中的基因型 - 表型相关性。

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