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COSMIC: somatic cancer genetics at high-resolution.COSMIC:高分辨率体细胞癌遗传学
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Integrated genomic DNA/RNA profiling of hematologic malignancies in the clinical setting.临床环境中血液系统恶性肿瘤的基因组DNA/RNA综合分析
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A Multiplexed Amplicon Approach for Detecting Gene Fusions by Next-Generation Sequencing.一种用于通过下一代测序检测基因融合的多重扩增子方法。
J Mol Diagn. 2016 Mar;18(2):165-75. doi: 10.1016/j.jmoldx.2015.10.002. Epub 2015 Dec 30.
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Landscape of gene fusions in epithelial cancers: seq and ye shall find.上皮性癌中基因融合的全景:测序,你就会发现。
Genome Med. 2015 Dec 18;7:129. doi: 10.1186/s13073-015-0252-1.
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Minimally invasive genomic and transcriptomic profiling of visceral cancers by next-generation sequencing of circulating exosomes.通过循环外泌体的下一代测序对内脏癌进行微创基因组和转录组分析。
Ann Oncol. 2016 Apr;27(4):635-41. doi: 10.1093/annonc/mdv604. Epub 2015 Dec 17.
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Durable Clinical Response to Entrectinib in NTRK1-Rearranged Non-Small Cell Lung Cancer.恩曲替尼治疗 NTRK1 重排非小细胞肺癌的持久临床应答。
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Acquired Resistance to the TRK Inhibitor Entrectinib in Colorectal Cancer.结直肠癌对 TRK 抑制剂恩曲替尼获得性耐药。
Cancer Discov. 2016 Jan;6(1):36-44. doi: 10.1158/2159-8290.CD-15-0940. Epub 2015 Nov 6.
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Clinical application of amplicon-based next-generation sequencing to therapeutic decision making in lung cancer.基于扩增子的下一代测序在肺癌治疗决策中的临床应用。
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High-throughput diagnostic profiling of clinically actionable gene fusions in lung cancer.肺癌中临床可操作基因融合的高通量诊断分析
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用于实体瘤激酶融合检测的靶向RNA测序分析方法的验证

Validation of a Targeted RNA Sequencing Assay for Kinase Fusion Detection in Solid Tumors.

作者信息

Reeser Julie W, Martin Dorrelyn, Miya Jharna, Kautto Esko A, Lyon Ezra, Zhu Eliot, Wing Michele R, Smith Amy, Reeder Matthew, Samorodnitsky Eric, Parks Hannah, Naik Karan R, Gozgit Joseph, Nowacki Nicholas, Davies Kurtis D, Varella-Garcia Marileila, Yu Lianbo, Freud Aharon G, Coleman Joshua, Aisner Dara L, Roychowdhury Sameek

机构信息

Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.

Ariad Pharmaceuticals, Cambridge, Massachusetts.

出版信息

J Mol Diagn. 2017 Sep;19(5):682-696. doi: 10.1016/j.jmoldx.2017.05.006. Epub 2017 Aug 9.

DOI:10.1016/j.jmoldx.2017.05.006
PMID:28802831
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5975628/
Abstract

Kinase gene fusions are important drivers of oncogenic transformation and can be inhibited with targeted therapies. Clinical grade diagnostics using RNA sequencing to detect gene rearrangements in solid tumors are limited, and the few that are available require prior knowledge of fusion break points. To address this, we have analytically validated a targeted RNA sequencing assay (OSU-SpARKFuse) for fusion detection that interrogates complete transcripts from 93 kinase and transcription factor genes. From a total of 74 positive and 36 negative control samples, OSU-SpARKFuse had 93.3% sensitivity and 100% specificity for fusion detection. Assessment of repeatability and reproducibility revealed 96.3% and 94.4% concordance between intrarun and interrun technical replicates, respectively. Application of this assay on prospective patient samples uncovered OLFM4 as a novel RET fusion partner in a small-bowel cancer and led to the discovery of a KLK2-FGFR2 fusion in a patient with prostate cancer who subsequently underwent treatment with a pan-fibroblast growth factor receptor inhibitor. Beyond fusion detection, OSU-SpARKFuse has built-in capabilities for discovery research, including gene expression analysis, detection of single-nucleotide variants, and identification of alternative splicing events.

摘要

激酶基因融合是致癌转化的重要驱动因素,可通过靶向治疗加以抑制。利用RNA测序检测实体瘤中基因重排的临床级诊断方法有限,且现有的少数方法需要预先了解融合断点。为解决这一问题,我们已通过分析验证了一种用于融合检测的靶向RNA测序检测方法(OSU-SpARKFuse),该方法可对93个激酶和转录因子基因的完整转录本进行检测。在总共74个阳性和36个阴性对照样本中,OSU-SpARKFuse在融合检测方面的灵敏度为93.3%,特异性为100%。对重复性和再现性的评估显示,批内和批间技术重复之间的一致性分别为96.3%和94.4%。将该检测方法应用于前瞻性患者样本,发现OLFM4是小肠癌中一种新的RET融合伴侣,并在一名前列腺癌患者中发现了KLK2-FGFR2融合,该患者随后接受了泛成纤维细胞生长因子受体抑制剂治疗。除融合检测外,OSU-SpARKFuse还具备用于探索性研究的内置功能,包括基因表达分析、单核苷酸变异检测和可变剪接事件识别。