RNA Extraction Method Impacts Quality Metrics and Sequencing Results in Formalin-Fixed, Paraffin-Embedded Tissue Samples

被引:4
|
作者
Decruyenaere, Philippe [1 ,2 ,3 ]
Verniers, Kimberly [2 ,3 ]
Poma-Soto, Franco [2 ,3 ]
Van Dorpe, Jo [4 ]
Offner, Fritz [1 ]
Vandesompele, Jo [2 ,3 ]
机构
[1] Ghent Univ Hosp, Dept Hematol, Ghent, Belgium
[2] Univ Ghent, Canc Res Inst Ghent, OncoRNALab, Ghent, Belgium
[3] Univ Ghent, Dept Biomol Med, Ghent, Belgium
[4] Ghent Univ Hosp, Ghent Univ, Dept Pathol, Ghent, Belgium
关键词
RNA extraction; FFPE; diffuse large B-cell lymphoma; NGS; RNA sequencing; B-CELL LYMPHOMA; EXPRESSION ANALYSIS; ARCHIVAL MATERIAL; STORAGE PERIOD; NUCLEIC-ACIDS; FIXATION; CLASSIFICATION; PURIFICATION; DURATION; BLOCKS;
D O I
10.1016/j.labinv.2022.100027
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Archived formalin-fixed, paraffin-embedded (FFPE) tissue samples are being increasingly used in molecular cancer research. Compared with fresh-frozen tissue, the nucleic acid analysis of FFPE tissue is technically more challenging. This study aimed to compare the impact of 3 different RNA extraction methods on yield, quality, and sequencing-based gene expression results in FFPE samples. RNA extraction was performed in 16 FFPE tumor specimens from patients with diffuse large B-cell lymphoma and in reference FFPE material from microsatellite-stable and microsatellite-instable cell lines (3 replicates each) using 2 silica-based procedures (A, miRNeasy FFPE; C, iCatcher FFPE Tissue RNA) and 1 isotachophoresis-based procedure (B, Ionic FFPE to Pure RNA). The RNA yield; RNA integrity, as reflected by the distribution value 200; and RNA purity, as reflected by the 260/280 and the 260/230 nm absorbance ratios, were determined. The RNA was sequenced on the NovaSeq 6000 instrument using the TruSeq RNA Exome and SMARTer Stranded Total RNA-Seq Pico v3 library preparations kits. Our results highlight the impact of RNA extraction methodology on both preanalytical and sequencing-based gene expression results. Overall, methods B and C outperformed method A because these showed significantly higher fractions of uniquely mapped reads, an increased number of detectable genes, a lower fraction of duplicated reads, and better representation of the B-cell receptor repertoire. Differences among the extraction methods were generally more explicit for the total RNA sequencing method than for the exome-capture sequencing method. Importantly, the predicative value of quality metrics varies among extraction kits, and caution should be applied when comparing and interpreting results obtained using different methods.(c) 2022 THE AUTHORS. Published by Elsevier Inc. on behalf of the United States & Canadian Academy of Pathology. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).
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页数:14
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