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Frozen Tumor Tissue Microarray Technology for Analysis of Tumor RNA, DNA, and Proteins

机译:冷冻肿瘤组织微阵列技术用于分析肿瘤RNA,DNA和蛋白质

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摘要

Tissue microarray technology is a new method used to analyze several hundred tumor samples on a single slide allowing high throughput analysis of genes and proteins on a large cohort. The original methodology involves coring tissues from paraffin-embedded tissue donor blocks and placing them into a single paraffin block. One difficulty with paraffin-embedded tissue relates to antigenic changes in proteins and mRNA degradation induced by the fixation and embedding process. We have modified this technology by using frozen tissues embedded in OCT compound as donor samples and arraying the specimens into a recipient OCT block. Tumor tissue is not fixed before embedding, and sections from the array are evaluated without fixation or postfixed according to the appropriate methodology used to analyze a specific gene at the DNA, RNA, and/or protein levels. While paraffin tissue arrays can be problematic for immunohistochemistry and for RNA in situ hybridization analyses, this method allows optimal evaluation by each technique and uniform fixation across the array panel. We show OCT arrays work well for DNA, RNA, and protein analyses, and may have significant advantages over the original technology for the assessment of some genes and proteins by improving both qualitative and quantitative results.
机译:组织微阵列技术是一种用于在单个载玻片上分析多个 肿瘤样品的新方法,从而可以对大型队列中的基因和蛋白质进行高通量 分析。最初的 方法涉及从石蜡包埋的组织 供体块中取出组织,并将它们放入单个石蜡块中。 石蜡包埋的组织的一个难题与固定 和包埋过程诱导的蛋白质中抗原性 变化和mRNA降解有关。我们使用嵌入在OCT化合物中的 冷冻组织作为供体样品,并 将样品排列到受体OCT块中,对这项技术进行了修改。嵌入前未固定肿瘤组织 ,并且根据用于分析特定肿瘤的适当 方法对阵列中的切片进行 评估而不进行固定或后固定DNA,RNA, 和/或蛋白质水平的基因。虽然石蜡组织阵列对于免疫组织化学和RNA原位杂交分析可能是有问题的,但该方法可以通过每种技术进行最佳评估,并且可以在整个固定范围内进行均匀固定。 阵列面板。我们显示了OCT阵列 可以很好地用于DNA,RNA和蛋白质分析,并且可能比原始技术具有显着的 优势,可以用于评估 some通过改善定性和定量结果而获得基因和蛋白质。

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  • 来源
    《American Journal of Pathology》 |2001年第5期|1645-1650|共6页
  • 作者单位

    From the Division of Hematology/Oncology, Department of Medicine, University of California, Los Angeles, School of Medicine, Los Angeles, California;

    From the Division of Hematology/Oncology, Department of Medicine, University of California, Los Angeles, School of Medicine, Los Angeles, California;

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