从存档的苏木精和伊红染色组织载玻片中提取DNA用于下游分子分析

P. Ramesh, Venkatesh Madegowda, S. Kumar, Shailashree Narasimha, Parichay S R, N. Manoli, Devananda Devegowda
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引用次数: 7

摘要

组织病理学染色的存档组织载玻片在医院档案中保存数年至数十年。它们是生物材料的最大可用来源,是可用于回顾性流行病学研究的潜在有用资源。从载玻片中回收的DNA可用于几个下游分子过程,包括聚合酶链反应,单核苷酸多态性分析和全基因组测序。这些载玻片上的DNA可以用来比较正常和患病组织的基因特征。然而,从存档的染色苏木精和伊红(H&E)载玻片中提取高质量的DNA仍然具有挑战性。目的为进一步的分子分析,从存档的h&e染色组织切片中提取DNA的新方案进行标准化。方法收集100份存档的h&e染色肿瘤切片,采用5种方法提取DNA。方法在脱蜡步骤、组织再水化、裂解时间和蛋白酶k的存在或不存在方面有所不同。提取的DNA用NanoDrop分光光度计定量,琼脂糖凝胶电泳分析质量。然后对每个样品进行聚合酶链反应(PCR),扩增内控基因GAPDH,从而确认DNA的完整性,进一步用于其他下游应用。结果在五种不同的测试方法中,第三种方法使用二甲苯进行组织脱胶,然后进行72 h的消化,没有蛋白酶K失活,产生的DNA数量最多,纯度高。与其他方法相比,收率显著提高。此外,90%的提取DNA显示可扩增的GAPDH基因。在这里,我们提出了一个循序渐进、成本效益高、可重复的方案,用于从存档的h&e染色的癌症组织切片中提取pcr友好的DNA,可用于进一步的下游分子应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DNA extraction from archived hematoxylin and eosin-stained tissue slides for downstream molecular analysis
BACKGROUND Histopathologically stained archived tissue slides are stored in hospital archives for years to decades. They are the largest available source of biological materials and are a potentially useful resource that can be used for retrospective epidemiological studies. DNA recovered from the slides can be used for several downstream molecular processes including polymerase chain reaction, single nucleotide polymorphism analysis, and whole genome sequencing. The DNA from these slides can be utilized to compare gene signatures of normal and diseased tissues. However, extraction of high-quality DNA from archived stained hematoxylin and eosin (H&E) slides remains challenging. AIM To standardize a new protocol for extracting DNA from archived H&E-stained tissue slides for further molecular assays. METHODS A total of 100 archived H&E-stained cancer slides were subjected to a total of five methods of DNA extraction. Methods were varied in the deparaffinization step, tissue rehydration, duration of lysis, and presence or absence of proteinase K. The extracted DNA was quantified using a NanoDrop spectrophometer and the quality was analyzed by agarose gel electrophoresis. Then each sample was subjected to polymerase chain reaction (PCR) to amplify the internal control gene GAPDH, thereby confirming the DNA intactness, which could be further utilized for other downstream applications. RESULTS Of the five different methods tested, the third method wherein xylene was used for tissue deparaffinization followed by 72 h of digestion and without proteinase K inactivation yielded the highest amount of DNA with good purity. The yield was significantly higher when compared to other methods. In addition, 90% of the extracted DNA showed amplifiable GAPDH gene. CONCLUSION Here we present a step-by-step, cost-effective, and reproducible protocol for the extraction of PCR-friendly DNA from archived H&E-stained cancer tissue slides that can be used for further downstream molecular applications.
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