Robustness of RNA sequencing on older formalin-fixed paraffin-embedded tissue from high-grade ovarian serous adenocarcinomas.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 16 10 2018
accepted: 12 04 2019
entrez: 7 5 2019
pubmed: 7 5 2019
medline: 14 1 2020
Statut: epublish

Résumé

Formalin-fixed paraffin-embedded (FFPE) tissues are among the most widely available clinical specimens. Their potential utility as a source of RNA for transcriptome studies would greatly enhance population-based cancer studies. Although preliminary studies suggest FFPE tissue may be used for RNA sequencing, the effect of storage time on these specimens needs to be determined. We conducted this study to determine whether RNA in archived FFPE high-grade ovarian serous adenocarcinomas from Surveillance, Epidemiology and End Results (SEER) registries was present in sufficient quantity and quality for RNA-Seq analysis. FFPE tissues, stored from 7 to 32 years, were obtained from three SEER sites. RNA was extracted, quantified, quality assessed, and subjected to RNA-Seq (a whole transcriptome sequencing technology). FFPE specimens stored for longer periods of time had poorer RNA sample quality as indicated by negative correlations between specimen storage time and fragment distribution values (DV). In addition, sample contamination was a common issue among the RNA, with 41 of 67 samples having 5% to 48% bacterial contamination. However, regardless of specimen storage time and bacterial contamination, 60% of the samples yielded data that enabled gene expression quantification, identifying more than 10,000 genes, with the correlations among most biological replicates above 0.7. This study demonstrates that FFPE high-grade ovarian serous adenocarcinomas specimens stored in repositories for up to 32 years and under varying storage conditions are a promising source of RNA for RNA-Seq. We also describe certain caveats to be considered when designing RNA-Seq studies using archived FFPE tissues.

Identifiants

pubmed: 31059554
doi: 10.1371/journal.pone.0216050
pii: PONE-D-18-29989
pmc: PMC6502345
doi:

Substances chimiques

RNA, Neoplasm 0
Formaldehyde 1HG84L3525

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0216050

Déclaration de conflit d'intérêts

The Leidos Biomedical Research, Inc affiliation does not alter the authors' adherence to all PLOS ONE policies on sharing data and materials.

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Auteurs

Yongmei Zhao (Y)

NCI CCR Sequencing Facility, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.
Advanced Biomedical and Computational Sciences, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.

Monika Mehta (M)

NCI CCR Sequencing Facility, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.

Ashley Walton (A)

NCI CCR Sequencing Facility, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.
Advanced Biomedical and Computational Sciences, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.

Keyur Talsania (K)

NCI CCR Sequencing Facility, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.
Advanced Biomedical and Computational Sciences, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.

Yelena Levin (Y)

NCI CCR Sequencing Facility, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.

Jyoti Shetty (J)

NCI CCR Sequencing Facility, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.

Elizabeth M Gillanders (EM)

Division of Cancer Control and Population Sciences (DCCPS), National Cancer Institute, Rockville, MD, United States of America.

Bao Tran (B)

NCI CCR Sequencing Facility, Frederick National Laboratory for Cancer Research, Frederick, MD, United States of America.

Danielle Mercatante Carrick (DM)

Division of Cancer Control and Population Sciences (DCCPS), National Cancer Institute, Rockville, MD, United States of America.

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Classifications MeSH