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首页> 外文期刊>Applied immunohistochemistry and molecular morphology: AIMM >Filter Paper-based Nucleic Acid Storage in High-throughput Solid Tumor Genotyping
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Filter Paper-based Nucleic Acid Storage in High-throughput Solid Tumor Genotyping

机译:高通量固体肿瘤基因分型中基于滤纸的核酸存储

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摘要

Molecular testing of tumors from formalin-fixed paraffin-embedded (FFPE) tissue blocks is central to clinical practice; however, it requires histology support and increases test turnaround time. Prospective fresh frozen tissue collection requires special handling, additional storage space, and may not be feasible for small specimens. Filter paper-based collection of tumor DNA reduces the need for histology support, requires little storage space, and preserves high-quality nucleic acid. We investigated the performance of tumor smears on filter paper in solid tumor genotyping, as compared with paired FFPE samples. Whatman FT A Micro Card (FT A preps) smears were prepared from 21 fresh tumor samples. A corresponding cytology smear was used to assess tumor cellularity and necrosis. DNA was isolated from FTA preps and FFPE core samples using automated methods and quantified using SYBR green dsDNA detection. Samples were genotyped for 471 mutations on a mass spectrophotometry-based platform (Sequenom). DNA concentrations from FTA preps and FFPE correlated for untreated carcinomas but not for mesenchymal tumors (Spearman a = 0.39 and
机译:用福尔马林固定石蜡包埋(FFPE)组织块对肿瘤进行分子检测是临床实践的核心。但是,它需要组织学支持并增加测试周转时间。准新鲜冷冻组织的采集需要特殊处理,需要额外的存储空间,对于小样本来说可能不可行。基于滤纸的肿瘤DNA收集减少了对组织学支持的需要,几乎不需要存储空间,并保留了高质量的核酸。与配对的FFPE样品相比,我们研究了在实体肿瘤基因分型中滤纸上肿瘤涂片的性能。从21个新鲜肿瘤样本中准备了Whatman FT A微型卡(FT A制剂)涂片。相应的细胞学涂片被用于评估肿瘤细胞和坏死。使用自动化方法从FTA制备物和FFPE核心样品中分离DNA,并使用SYBR green dsDNA检测进行定量。在基于质谱的平台(Sequenom)上对471个突变进行基因分型。 FTA preps和FFPE的DNA浓度与未经治疗的癌相关,而与间充质肿瘤无相关性(分别为Spearman a = 0.39和

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