Optimization of recovery of RNA from formalin-fixed, paraffin-embedded tissue

被引:67
作者
Chung, Joon-Yong
Braunschweig, Till
Hewitt, Stephen M.
机构
[1] NCI, TARP Lab, Ctr Adv Technol, Lab Pathol,NIH, Bethesda, MD 20892 USA
[2] Inje Univ, Coll Med, Pharmaco Genom Res Ctr, Pusan 614735, South Korea
关键词
RNA; formalin-fixed paraffin-embedded tissue; multiplex RT-PCR; RNAlater;
D O I
10.1097/01.pdm.0000213468.91139.2d
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Formalin-fixed, paraffin-embedded (FFPE) tissue is the most common specimen available for application of diagnostic assays on tissue after microscopic examination. Not only is there a substantial archive of tissue available, but FFPE tissue remains the best method of preparation for microscopic examination in a routine clinical environment. Molecular assays, especially reverse transcription and polymerase chain reaction and expression array-based assays, offer significant potential as diagnostic, prognostic, and predictive tools, but require high quality RNA. Herein, we have optimized a reliable RNA extraction method for FFPE tissue. It is based on deparaffinization at high temperature coupled with a 3-day lysis at 65 degrees C. The average total RNA yield is 4.5 to 5.5 pg per 1 mu m(3) of archival FFPE tissue, and 260/280 ratios are between 1.80 and 1.95. The extracted RNA has a modal fragment length between 100 and 200 nt by the Bioanalyzer analysis. Although modal lengths of RNA fragments were shorter, reverse transcription and polymerase chain reaction was able to amplify amplicons in range of 300 bp. Pretreatment with RNA later followed by formalin fixation did not result in improving the RNA quality, but did improve RNA yield. Our method improves the utility of FFPE tissue for molecular profiling studies.
引用
收藏
页码:229 / 236
页数:8
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