Evaluation of DNA and RNA quality from archival formalin‐fixed paraffin‐embedded tissue for next‐generation sequencing – Retrospective study in Japanese single institution
Genetic analysis on formalin‐fixed paraffin‐embedded (FFPE) tissue specimens has become a mainstream method, from conventional direct sequencing to comprehensive analysis using next‐generation sequencing (NGS). In this study, we evaluated the quality of DNA and RNA extracted from FFPE sections, deri...
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Veröffentlicht in: | Pathology international 2020-09, Vol.70 (9), p.602-611 |
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creator | Fujii, Tomomi Uchiyama, Tomoko Matsuoka, Minami Myojin, Tomoya Sugimoto, Sumire Nitta, Yuji Okabe, Fumi Sugimoto, Aya Sekita‐Hatakeyama, Yoko Morita, Kohei Itami, Hiroe Hatakeyama, Kinta Ohbayashi, Chiho |
description | Genetic analysis on formalin‐fixed paraffin‐embedded (FFPE) tissue specimens has become a mainstream method, from conventional direct sequencing to comprehensive analysis using next‐generation sequencing (NGS). In this study, we evaluated the quality of DNA and RNA extracted from FFPE sections, derived from surgical specimens of different tumor types. Electrophoresis was performed using a 4200 TapeStation to evaluate DNA and RNA fragmentation. DNA Ct values were higher and significantly increased over a period of 4 years compared with those from cell lines or frozen tissues. The RNA integrity number equivalent (RIN) ranged from 1 to 4.1 and DV200 ranged from 7.3 to 81%. Twelve of the 108 cases were analyzed by NGS using the AmpliSeq Cancer HotSpot Panel v2 on a Miniseq system. A sufficient number of reads and coverage were obtained in all cases. Our results revealed that NGS analysis was sufficient for FFPE‐derived DNA within 4 years of preservation. Conversely, approximately 20% of the RNA derived from FFPE within 4 years from the collection could be inappropriate for gene analysis based on RIN and DV200. It was suggested that FFPE would be adequate for genetic analysis, although it is desirable to store frozen specimens for the tumor tissues to be subjected to genetic analysis. |
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In this study, we evaluated the quality of DNA and RNA extracted from FFPE sections, derived from surgical specimens of different tumor types. Electrophoresis was performed using a 4200 TapeStation to evaluate DNA and RNA fragmentation. DNA Ct values were higher and significantly increased over a period of 4 years compared with those from cell lines or frozen tissues. The RNA integrity number equivalent (RIN) ranged from 1 to 4.1 and DV200 ranged from 7.3 to 81%. Twelve of the 108 cases were analyzed by NGS using the AmpliSeq Cancer HotSpot Panel v2 on a Miniseq system. A sufficient number of reads and coverage were obtained in all cases. Our results revealed that NGS analysis was sufficient for FFPE‐derived DNA within 4 years of preservation. Conversely, approximately 20% of the RNA derived from FFPE within 4 years from the collection could be inappropriate for gene analysis based on RIN and DV200. 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It was suggested that FFPE would be adequate for genetic analysis, although it is desirable to store frozen specimens for the tumor tissues to be subjected to genetic analysis.</description><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA fragmentation</subject><subject>DNA sequencing</subject><subject>Electrophoresis</subject><subject>Formaldehyde</subject><subject>Genetic analysis</subject><subject>NGS</subject><subject>Paraffin</subject><subject>Paraffins</subject><subject>PCR</subject><subject>Preservation</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>stored FFPE tissue</subject><subject>Tissues</subject><subject>Tumors</subject><issn>1320-5463</issn><issn>1440-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kUFu1jAQhSNEJUrLghtYYgOLtB7HSZxlVQotqgqqYB05zri4SpzUdtr-ux6hEkfhRj0J8zeskPBmrOfPM89-WfYW-AHQOpydPwDRVM2LbBek5DkoUb-kfSF4XsqqeJW9jvGac6iLiu9mv09u9bDo5CbPJss-Xhwx7Xt2SfVm0YNLG2bDNDIdzE9HKLNTGEn3Tw-P1t1jz2YdtLXPAo4d9j1pycW44JZlHu8THV2hx7COiXizoDfOX7Gnh1_sElOY4owmuVtkMS39hjnPvuhZe4ykEDggSTG5tGw77Gc7Vg8R3_yte9mPTyffj0_z86-fz46PznMjBW9ypSqAqihKrpSpQCglu14UAEIUHHpdNR0gmN4KUytbisZg03WGl6VuJO91sZe9X_vOYSLLMbWjiwaHgYxNS2yFBEkfWSkg9N0_6PW0BE_uiJIgOK95TdSHlTL04hjQtnNwow6bFni7ja-l-Nrn-Ig9XNk7N-Dm_2D77exivfEHfLCiqg</recordid><startdate>202009</startdate><enddate>202009</enddate><creator>Fujii, Tomomi</creator><creator>Uchiyama, Tomoko</creator><creator>Matsuoka, Minami</creator><creator>Myojin, Tomoya</creator><creator>Sugimoto, Sumire</creator><creator>Nitta, Yuji</creator><creator>Okabe, Fumi</creator><creator>Sugimoto, Aya</creator><creator>Sekita‐Hatakeyama, Yoko</creator><creator>Morita, Kohei</creator><creator>Itami, Hiroe</creator><creator>Hatakeyama, Kinta</creator><creator>Ohbayashi, Chiho</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T5</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7207-4127</orcidid><orcidid>https://orcid.org/0000-0002-7916-6323</orcidid></search><sort><creationdate>202009</creationdate><title>Evaluation of DNA and RNA quality from archival formalin‐fixed paraffin‐embedded tissue for next‐generation sequencing – Retrospective study in Japanese single institution</title><author>Fujii, Tomomi ; Uchiyama, Tomoko ; Matsuoka, Minami ; Myojin, Tomoya ; Sugimoto, Sumire ; Nitta, Yuji ; Okabe, Fumi ; Sugimoto, Aya ; Sekita‐Hatakeyama, Yoko ; Morita, Kohei ; Itami, Hiroe ; Hatakeyama, Kinta ; Ohbayashi, Chiho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4209-886116335088c612884bd231122301da69b1e1cdf2c78f529ce9bbc055a940da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA fragmentation</topic><topic>DNA sequencing</topic><topic>Electrophoresis</topic><topic>Formaldehyde</topic><topic>Genetic analysis</topic><topic>NGS</topic><topic>Paraffin</topic><topic>Paraffins</topic><topic>PCR</topic><topic>Preservation</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>stored FFPE tissue</topic><topic>Tissues</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujii, Tomomi</creatorcontrib><creatorcontrib>Uchiyama, Tomoko</creatorcontrib><creatorcontrib>Matsuoka, Minami</creatorcontrib><creatorcontrib>Myojin, Tomoya</creatorcontrib><creatorcontrib>Sugimoto, Sumire</creatorcontrib><creatorcontrib>Nitta, Yuji</creatorcontrib><creatorcontrib>Okabe, Fumi</creatorcontrib><creatorcontrib>Sugimoto, Aya</creatorcontrib><creatorcontrib>Sekita‐Hatakeyama, Yoko</creatorcontrib><creatorcontrib>Morita, Kohei</creatorcontrib><creatorcontrib>Itami, Hiroe</creatorcontrib><creatorcontrib>Hatakeyama, Kinta</creatorcontrib><creatorcontrib>Ohbayashi, Chiho</creatorcontrib><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pathology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujii, Tomomi</au><au>Uchiyama, Tomoko</au><au>Matsuoka, Minami</au><au>Myojin, Tomoya</au><au>Sugimoto, Sumire</au><au>Nitta, Yuji</au><au>Okabe, Fumi</au><au>Sugimoto, Aya</au><au>Sekita‐Hatakeyama, Yoko</au><au>Morita, Kohei</au><au>Itami, Hiroe</au><au>Hatakeyama, Kinta</au><au>Ohbayashi, Chiho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of DNA and RNA quality from archival formalin‐fixed paraffin‐embedded tissue for next‐generation sequencing – Retrospective study in Japanese single institution</atitle><jtitle>Pathology international</jtitle><date>2020-09</date><risdate>2020</risdate><volume>70</volume><issue>9</issue><spage>602</spage><epage>611</epage><pages>602-611</pages><issn>1320-5463</issn><eissn>1440-1827</eissn><abstract>Genetic analysis on formalin‐fixed paraffin‐embedded (FFPE) tissue specimens has become a mainstream method, from conventional direct sequencing to comprehensive analysis using next‐generation sequencing (NGS). In this study, we evaluated the quality of DNA and RNA extracted from FFPE sections, derived from surgical specimens of different tumor types. Electrophoresis was performed using a 4200 TapeStation to evaluate DNA and RNA fragmentation. DNA Ct values were higher and significantly increased over a period of 4 years compared with those from cell lines or frozen tissues. The RNA integrity number equivalent (RIN) ranged from 1 to 4.1 and DV200 ranged from 7.3 to 81%. Twelve of the 108 cases were analyzed by NGS using the AmpliSeq Cancer HotSpot Panel v2 on a Miniseq system. A sufficient number of reads and coverage were obtained in all cases. Our results revealed that NGS analysis was sufficient for FFPE‐derived DNA within 4 years of preservation. Conversely, approximately 20% of the RNA derived from FFPE within 4 years from the collection could be inappropriate for gene analysis based on RIN and DV200. 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subjects | Deoxyribonucleic acid DNA DNA fragmentation DNA sequencing Electrophoresis Formaldehyde Genetic analysis NGS Paraffin Paraffins PCR Preservation Ribonucleic acid RNA stored FFPE tissue Tissues Tumors |
title | Evaluation of DNA and RNA quality from archival formalin‐fixed paraffin‐embedded tissue for next‐generation sequencing – Retrospective study in Japanese single institution |
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