Bapat Prachi R, Epari Sridhar, Joshi Pradnya V, Dhanavade Dipika S, Rumde Rachna H, Gurav Mamta Y, Shetty Omshree A, Desai Sangeeta B
Molecular Pathology, Tata Memorial Hospital, Homi Bhabha National Institute, Mumbai, India.
Am J Clin Pathol. 2022 Dec 1;158(6):739-749. doi: 10.1093/ajcp/aqac122.
Good-quality nucleic acid extraction from formalin-fixed, paraffin-embedded (FFPE) specimens remains a challenge in molecular-oncopathology practice. This study evaluates the efficacy of an in-house developed FFPE extraction buffer compared with other commercially available kits.
Eighty FFPE specimens processed in different surgical pathology laboratories formed the study sample. DNA extraction was performed using three commercial kits and the in-house developed FFPE extraction buffer. DNA yield was quantified by a NanoDrop spectrophotometer and Qubit Fluorometer, and its purity was measured by the 260/280-nm ratio. A fragment analyzer system was used for accurate sizing of DNA fragments of FFPE DNA. The downstream effects of all extraction methods were evaluated by polymerase chain reaction (PCR) and Sanger sequencing.
In comparison with the commercial kits, the in-house buffer yielded higher DNA quantity and quality number (P < .0001). In addition, DNA integrity and fragment size were preserved in a significantly greater number of samples isolated with the in-house buffer (P < .05). The target PCR amplification rate with the in-house buffer extracted samples was also significantly higher, with 98% of the samples showing interpretable sequencing results.
The in-house developed FFPE extraction buffer performed superior to other methods in terms of suitability for downstream applications, time, cost-efficiency, and ease of performance.
从福尔马林固定石蜡包埋(FFPE)标本中提取高质量核酸在分子肿瘤病理学实践中仍然是一项挑战。本研究评估了一种自行研制的FFPE提取缓冲液与其他市售试剂盒相比的效果。
在不同外科病理实验室处理的80个FFPE标本构成了研究样本。使用三种商业试剂盒和自行研制的FFPE提取缓冲液进行DNA提取。用NanoDrop分光光度计和Qubit荧光计对DNA产量进行定量,并通过260/280纳米比值测量其纯度。使用片段分析仪系统对FFPE DNA的片段进行精确大小测定。通过聚合酶链反应(PCR)和桑格测序评估所有提取方法的下游效应。
与商业试剂盒相比,自制缓冲液产生的DNA数量和质量更高(P <.0001)。此外,使用自制缓冲液分离的样本中,DNA完整性和片段大小得到显著保留的样本数量更多(P <.05)。使用自制缓冲液提取的样本的目标PCR扩增率也显著更高,98%的样本显示出可解释的测序结果。
自行研制的FFPE提取缓冲液在下游应用的适用性、时间、成本效益和操作简便性方面优于其他方法。