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用于靶向新一代测序的福尔马林固定石蜡包埋组织块RNA提取方法的优化

Optimization of RNA Extraction from Formalin-Fixed Paraffin-Embedded Blocks for Targeted Next-Generation Sequencing.

作者信息

Choi Yoojin, Kim Aeree, Kim Jinkyoung, Lee Jinhwan, Lee Soo Yeon, Kim Chungyeul

机构信息

Department of Pathology, Korea University Guro Hospital, Seoul, Korea.

出版信息

J Breast Cancer. 2017 Dec;20(4):393-399. doi: 10.4048/jbc.2017.20.4.393. Epub 2017 Dec 19.

Abstract

PURPOSE

Breast cancer has a high prevalence in Korea. To achieve personalized therapy for breast cancer, long-term follow-up specimens are needed for next-generation sequencing (NGS) and multigene analysis. Formalin-fixed paraffin-embedded (FFPE) samples are easier to store than fresh frozen (FF) samples. The objective of this study was to optimize RNA extraction from FFPE blocks for NGS.

METHODS

RNA quality from FF and FFPE tissues (n=5), expected RNA amount per unit area, the relationship between archiving time and quantity/quality of FFPE-extracted RNA (n=14), differences in quantitative real-time polymerase chain reaction (qRT-PCR) and NGS results, and comparisons of both techniques with tissue processing at different institutions (n=96) were determined in this study.

RESULTS

The quality of RNA did not show any statistically significant difference between paired FF and FFPE specimens (=0.49). Analysis of tumor cellularity gave an expected RNA amount of 33.25 ng/mm. Archiving time affected RNA quality, showing a negative correlation with RNA integrity number and a positive correlation with threshold cycle. However, RNA from samples as old as 10 years showed a 100% success rate in qRT-PCR using short primers, showing that the effect of archiving time can be overcome by proper experiment design. NGS showed a higher success rate than qRT-PCR. Specimens from institution B (n=46), which were often stored in a refrigerator for more than 6 hours and fixed without slicing, showed lower success rates and worse results than specimens from the other institutes.

CONCLUSION

Archived FFPE tissues can be used to extract RNA for NGS if they are properly processed before fixation. The expected amount of RNA per unit size calculated in this study will be useful for other researchers.

摘要

目的

乳腺癌在韩国的发病率很高。为实现乳腺癌的个性化治疗,需要长期随访标本进行下一代测序(NGS)和多基因分析。福尔马林固定石蜡包埋(FFPE)样本比新鲜冷冻(FF)样本更易于保存。本研究的目的是优化从FFPE组织块中提取RNA用于NGS。

方法

本研究测定了FF和FFPE组织(n = 5)的RNA质量、单位面积预期RNA量、存档时间与FFPE提取RNA的量/质量之间的关系(n = 14)、定量实时聚合酶链反应(qRT-PCR)和NGS结果的差异,以及两种技术在不同机构进行组织处理时的比较(n = 96)。

结果

配对的FF和FFPE标本之间的RNA质量没有显示出任何统计学上的显著差异(P = 0.49)。肿瘤细胞含量分析得出预期RNA量为33.25 ng/mm²。存档时间影响RNA质量,与RNA完整性数值呈负相关,与阈值循环呈正相关。然而,使用短引物的qRT-PCR显示,来自10年之久样本的RNA成功率为100%,这表明通过适当的实验设计可以克服存档时间的影响。NGS显示出比qRT-PCR更高的成功率。机构B的标本(n = 46)经常在冰箱中保存超过6小时且未切片固定,其成功率低于其他机构的标本,结果也更差。

结论

如果在固定前进行适当处理,存档的FFPE组织可用于提取RNA进行NGS。本研究计算出的每单位大小的预期RNA量将对其他研究人员有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff05/5744000/965522a5d5ee/jbc-20-393-g001.jpg

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