首页> 美国卫生研究院文献>The Journal of Molecular Diagnostics : JMD >Technical Reproducibility of Single-Nucleotide and Size-Based DNA Biomarker Assessment Using DNA Extracted from Formalin-Fixed Paraffin-Embedded Tissues
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Technical Reproducibility of Single-Nucleotide and Size-Based DNA Biomarker Assessment Using DNA Extracted from Formalin-Fixed Paraffin-Embedded Tissues

机译:使用从福尔马林固定石蜡包埋的组织中提取的DNA提取单核苷酸和基于大小的DNA生物标记物的技术可重复性

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摘要

DNA extracted from formalin-fixed, paraffin-embedded (FFPE) tissues has been used in the past to analyze genetic polymorphisms. We evaluated the technical reproducibility of different types of assays for gene polymorphisms using DNA extracted from FFPE material. By using the MassARRAY iPLEX system, we investigated polymorphisms in DPYD (rs1801159 and rs3918290), UMPS (rs1801019), ERCC1 (rs11615), ERCC1 (rs3212986), and ERCC2 (rs13181) in 56 FFPE DNA samples. By using PCR, followed by size-based gel electrophoresis, we also examined TYMS 5′ untranslated region 2R/3R repeats and GSTT1 deletions in 50 FFPE DNA samples and 34 DNAs extracted from fresh-frozen tissues and cell lines. Each polymorphism was analyzed by two independent runs. We found that iPLEX biomarker assays measuring single-nucleotide polymorphisms provided consistent concordant results. However, by using FFPE DNA, size-based PCR biomarkers (GSTT1 and TYMS 5′ untranslated region) were discrepant in 32.7% (16/49, with exact 95% CI, 19.9%–47.5%; exact binomial confidence limit test) and 4.2% (2/48, with exact 95% CI, 0.5%–14.3%) of cases, respectively, whereas no discrepancies were observed using intact genomic DNA. Our findings suggest that DNA from FFPE material can be used to reliably test single-nucleotide polymorphisms. However, results based on size-based PCR biomarkers, and particularly GSTT1 deletions, using FFPE DNA need to be interpreted with caution. Independent repeated assays should be performed on all cases to assess potential discrepancies.
机译:从福尔马林固定,石蜡包埋(FFPE)的组织中提取的DNA过去曾用于分析遗传多态性。我们使用从FFPE材料中提取的DNA评估了基因多态性的不同类型检测方法的技术可重复性。通过使用MassARRAY iPLEX系统,我们研究了56个FFPE DNA样品中DPYD(rs1801159和rs3918290),UMPS(rs1801019),ERCC1(rs11615),ERCC1(rs3212986)和ERCC2(rs13181)的多态性。通过使用PCR,然后进行基于大小的凝胶电泳,我们还检查了TYMS 5'非翻译区2R / 3R重复和GSTT1缺失的50个FFPE DNA样品和34个从新鲜冷冻的组织和细胞系中提取的DNA。通过两个独立的运行来分析每个多态性。我们发现,测量单核苷酸多态性的iPLEX生物标志物测定提供了一致的结果。但是,通过使用FFPE DNA,基于大小的PCR生物标记(GSTT1和TYMS 5'非翻译区)在32.7%(16/49,准确的95%CI,19.9%-47.5%;准确的二项式置信限度检验)中有差异。分别有4.2%(2/48,准确的95%CI,0.5%–14.3%)的病例,而使用完整的基因组DNA则没有发现差异。我们的发现表明,来自FFPE材料的DNA可用于可靠地测试单核苷酸多态性。但是,使用FFPE DNA基于大小的PCR生物标志物,尤其是GSTT1缺失的结果需要谨慎解释。应该对所有病例进行独立的重复测定,以评估潜在的差异。

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