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RNA extraction from ten year old formalin-fixed paraffin-embedded breast cancer samples: a comparison of column purification and magnetic bead-based technologies

机译:从十岁的福尔马林固定石蜡包埋的乳腺癌样品中提取RNA:柱纯化和基于磁珠的技术比较

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摘要

BackgroundThe development of protocols for RNA extraction from paraffin-embedded samples facilitates gene expression studies on archival samples with known clinical outcome. Older samples are particularly valuable because they are associated with longer clinical follow up. RNA extracted from formalin-fixed paraffin-embedded (FFPE) tissue is problematic due to chemical modifications and continued degradation over time. We compared quantity and quality of RNA extracted by four different protocols from 14 ten year old and 14 recently archived (three to ten months old) FFPE breast cancer tissues. Using three spin column purification-based protocols and one magnetic bead-based protocol, total RNA was extracted in triplicate, generating 336 RNA extraction experiments. RNA fragment size was assayed by reverse transcription-polymerase chain reaction (RT-PCR) for the housekeeping gene glucose-6-phosphate dehydrogenase (G6PD), testing primer sets designed to target RNA fragment sizes of 67 bp, 151 bp, and 242 bp.
机译:背景技术从石蜡包埋的样品中提取RNA的协议的发展有助于对具有已知临床结果的档案样品进行基因表达研究。较旧的样品特别有价值,因为它们与更长的临床随访时间有关。从福尔马林固定石蜡包埋(FFPE)组织中提取的RNA由于化学修饰和随着时间的推移持续降解而存在问题。我们比较了四种不同方案提取的RNA的数量和质量,这些协议分别来自14个10岁的FFPE乳腺癌组织和14个最近归档的(3到10个月大)FFPE乳腺癌组织。使用三种基于旋转柱纯化的方案和一种基于磁珠的方案,一式三份提取总RNA,从而产生336个RNA提取实验。通过管家基因葡萄糖6磷酸脱氢酶(G6PD)的逆转录聚合酶链反应(RT-PCR)分析了RNA片段的大小,测试了设计为靶向67 bp,151 bp和242 bp RNA片段大小的引物组。

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