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通过从福尔马林固定石蜡包埋标本中进行靶向富集,对癌症进行全面的分子谱分析。

Comprehensive assay for the molecular profiling of cancer by target enrichment from formalin-fixed paraffin-embedded specimens.

机构信息

Division of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.

Genome Science Division, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.

出版信息

Cancer Sci. 2019 Apr;110(4):1464-1479. doi: 10.1111/cas.13968. Epub 2019 Mar 5.

Abstract

Tumor molecular profiling is becoming a standard of care for patients with cancer, but the optimal platform for cancer sequencing remains undetermined. We established a comprehensive assay, the Todai OncoPanel (TOP), which consists of DNA and RNA hybridization capture-based next-generation sequencing panels. A novel method for target enrichment, named the junction capture method, was developed for the RNA panel to accurately and cost-effectively detect 365 fusion genes as well as aberrantly spliced transcripts. The TOP RNA panel can also measure the expression profiles of an additional 109 genes. The TOP DNA panel was developed to detect single nucleotide variants and insertions/deletions for 464 genes, to calculate tumor mutation burden and microsatellite instability status, and to infer chromosomal copy number. Clinically relevant somatic mutations were identified in 32.2% (59/183) of patients by prospective TOP testing, signifying the clinical utility of TOP for providing personalized medicine to cancer patients.

摘要

肿瘤分子分析正在成为癌症患者的标准治疗方法,但癌症测序的最佳平台仍未确定。我们建立了一个综合的检测方法,即东大癌症基因检测面板(TOP),它由 DNA 和 RNA 杂交捕获的下一代测序面板组成。我们还开发了一种新的靶向富集方法,称为连接捕获法,用于 RNA 面板,以准确且经济高效地检测 365 个融合基因和异常剪接的转录本。TOP RNA 面板还可以测量另外 109 个基因的表达谱。TOP DNA 面板用于检测 464 个基因的单核苷酸变异和插入/缺失,计算肿瘤突变负担和微卫星不稳定性状态,并推断染色体拷贝数。通过前瞻性的 TOP 检测,有 32.2%(59/183)的患者发现了临床相关的体细胞突变,这表明 TOP 在为癌症患者提供个性化药物方面具有临床应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2612/6447855/4b246d5e3d5a/CAS-110-1464-g001.jpg

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