Wang Lan, Yekula Anudeep, Muralidharan Koushik, Small Julia L, Rosh Zachary S, Kang Keiko M, Carter Bob S, Balaj Leonora
Department of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02115, USA.
School of Medicine, University of California San Diego, San Diego, CA 92092, USA.
Cancers (Basel). 2020 May 13;12(5):1219. doi: 10.3390/cancers12051219.
Sequencing studies have provided novel insights into the heterogeneous molecular landscape of glioblastoma (GBM), unveiling a subset of patients with gene fusions. Tissue biopsy is highly invasive, limited by sampling frequency and incompletely representative of intra-tumor heterogeneity. Extracellular vesicle-based liquid biopsy provides a minimally invasive alternative to diagnose and monitor tumor-specific molecular aberrations in patient biofluids. Here, we used targeted RNA sequencing to screen GBM tissue and the matched plasma of patients ( = 9) for RNA fusion transcripts. We identified two novel fusion transcripts in GBM tissue and five novel fusions in the matched plasma of GBM patients. The fusion transcripts FGFR3-TACC3 and VTI1A-TCF7L2 were detected in both tissue and matched plasma. A longitudinal follow-up of a GBM patient with a FGFR3-TACC3 positive glioma revealed the potential of monitoring RNA fusions in plasma. In summary, we report a sensitive RNA-seq-based liquid biopsy strategy to detect RNA level fusion status in the plasma of GBM patients.
测序研究为胶质母细胞瘤(GBM)异质性分子格局提供了新见解,揭示了一部分存在基因融合的患者。组织活检具有高度侵入性,受采样频率限制且不能完全代表肿瘤内异质性。基于细胞外囊泡的液体活检为诊断和监测患者生物流体中的肿瘤特异性分子畸变提供了一种微创替代方法。在此,我们使用靶向RNA测序对GBM组织及匹配的患者血浆(n = 9)进行RNA融合转录本筛查。我们在GBM组织中鉴定出两种新型融合转录本,在GBM患者匹配血浆中鉴定出五种新型融合。融合转录本FGFR3-TACC3和VTI1A-TCF7L2在组织和匹配血浆中均被检测到。对一名FGFR3-TACC3阳性胶质瘤GBM患者的纵向随访揭示了监测血浆中RNA融合的潜力。总之,我们报告了一种基于RNA测序的灵敏液体活检策略,用于检测GBM患者血浆中的RNA水平融合状态。