Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue

被引:84
作者
Carrick, Danielle Mercatante [1 ]
Mehaffey, Michele G. [2 ,3 ]
Sachs, Michael C. [4 ]
Altekruse, Sean [1 ]
Camalier, Corinne [2 ,3 ]
Chuaqui, Rodrigo [4 ]
Cozen, Wendy [5 ]
Das, Biswajit [2 ,3 ]
Hernandez, Brenda Y. [6 ]
Lih, Chih-Jian [2 ,3 ]
Lynch, Charles F. [7 ]
Makhlouf, Hala [4 ]
McGregor, Paul [2 ,3 ]
McShane, Lisa M. [4 ]
Rohan, JoyAnn Phillips [2 ,3 ]
Walsh, William D. [2 ,3 ]
Williams, Paul M. [2 ,3 ]
Gillanders, Elizabeth M. [1 ]
Mechanic, Leah E. [1 ]
Schully, Sheri D. [1 ]
机构
[1] NCI, DCCPS, Rockville, MD 20850 USA
[2] Leidos Biomed Res Inc, Mol Characterizat & Clin Assay Dev Lab, Frederick, MD 21702 USA
[3] Frederick Natl Lab Canc Res, Frederick, MD 21702 USA
[4] NCI, DCTD, Rockville, MD 20850 USA
[5] Univ So Calif, USC Keck Sch Med, Los Angeles, CA 90089 USA
[6] Univ Hawaii, Ctr Canc, Honolulu, HI 96813 USA
[7] Univ Iowa, Coll Publ Hlth, Dept Epidemiol, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
FFPE TUMOR-TISSUES; SOMATIC MUTATIONS; CANCER; IDENTIFICATION; CONFIDENCE; CARCINOMA; SAMPLES; FROZEN;
D O I
10.1371/journal.pone.0127353
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Next Generation Sequencing (NGS) technologies are used to detect somatic mutations in tumors and study germ line variation. Most NGS studies use DNA isolated from whole blood or fresh frozen tissue. However, formalin-fixed paraffin-embedded (FFPE) tissues are one of the most widely available clinical specimens. Their potential utility as a source of DNA for NGS would greatly enhance population-based cancer studies. While preliminary studies suggest FFPE tissue may be used for NGS, the feasibility of using archived FFPE specimens in population based studies and the effect of storage time on these specimens needs to be determined. We conducted a study to determine whether DNA in archived FFPE high-grade ovarian serous adenocarcinomas from Surveillance, Epidemiology and End Results (SEER) registries Residual Tissue Repositories (RTR) was present in sufficient quantity and quality for NGS assays. Fifty-nine FFPE tissues, stored from 3 to 32 years, were obtained from three SEER RTR sites. DNA was extracted, quantified, quality assessed, and subjected to whole exome sequencing (WES). Following DNA extraction, 58 of 59 specimens (98%) yielded DNA and moved on to the library generation step followed by WES. Specimens stored for longer periods of time had significantly lower coverage of the target region (6% lower per 10 years, 95% CI: 3-10%) and lower average read depth (40x lower per 10 years, 95% CI: 18-60), although sufficient quality and quantity of WES data was obtained for data mining. Overall, 90% (53/59) of specimens provided usable NGS data regardless of storage time. This feasibility study demonstrates FFPE specimens acquired from SEER registries after varying lengths of storage time and under varying storage conditions are a promising source of DNA for NGS.
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