DETERMINING GOOD DNA QUALITY OF FFPE CRC TISSUES VIA A MACRODISSECTION-DNA EXTRACTION PROTOCOL

Ng Phei Ying, S. N. Mohd Nafi
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Abstract

A good DNA quality and quantity from a formalin-fixed paraffin-embedded (FFPE) tissue sample is crucial for a better downstream genomic analysis. Previous research has focused on comparing FFPE DNA extraction kits, but the improvement in kit outcome has yet to be studied. This study aimed to make some modifications to a selected Qiagen DNA extraction manual protocol using a manual macrodissected FFPE colorectal cancer (CRC) tissue sample. A variety of DNA extraction protocol-related variables, such as washing steps, tissue sections, and FFPE tissue age have been investigated to determine the DNA quality and quantity of the FFPE tissues. The prechilled absolute ethanol washing step showed the highest DNA concentration with good purity ratios. One, two, or four tissue sections using the washing step were sufficient to obtain adequate DNA concentrations with acceptable DNA purity ratios. 1% or 2% agarose gel electrophoresis with the pre-casting method allowed better visualisation of FFPE DNA. Based on the ideal quality and quantity, we chose a manual macrodissected DNA extraction protocol employing 4 x 10 µm FFPE tissue sections generated in recent years with an optimised prechilled absolute ethanol washing step.
通过大切片-DNA 提取规程确定 ffpe crc 组织的良好 dna 质量
从福尔马林固定石蜡包埋(FFPE)组织样本中提取高质量和高数量的 DNA 对于更好地进行下游基因组分析至关重要。以往的研究主要集中在对 FFPE DNA 提取试剂盒的比较上,但对试剂盒结果的改进还有待研究。本研究的目的是利用人工大切片FFPE结直肠癌(CRC)组织样本,对选定的Qiagen DNA提取手工方案进行一些修改。为了确定FFPE组织的DNA质量和数量,研究人员调查了与DNA提取方案相关的各种变量,如清洗步骤、组织切片和FFPE组织年龄。预冷绝对乙醇洗涤步骤显示出最高的 DNA 浓度和良好的纯度比。一个、两个或四个组织切片使用洗涤步骤足以获得足够的 DNA 浓度和可接受的 DNA 纯度比。采用预铸法进行 1%或 2%琼脂糖凝胶电泳能更好地观察 FFPE DNA。基于理想的质量和数量,我们选择了一种手动大切片 DNA 提取方案,采用近几年产生的 4 x 10 µm FFPE 组织切片,并优化了预冷绝对乙醇清洗步骤。
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