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Small Nucleolar RNA Score: An Assay to Detect Formalin-Overfixed Tissue
Although there are millions of formalin-fixed paraffin-embedded (FFPE) tissue blocks potentially available for scientific research, many are of questionable quality, partly due to unknown fixation conditions. We analyzed FFPE tissue biospecimens as part of the NCI Biospecimen Preanalytical Variables...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308291/ https://www.ncbi.nlm.nih.gov/pubmed/30234371 http://dx.doi.org/10.1089/bio.2018.0042 |
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author | Ammerlaan, Wim Trouet, Johanna Sachs, Michael C. Guan, Ping Carithers, Latarsha Lambert, Pauline Frasquilho, Sonia Antunes, Laurent Kofanova, Olga Rohrer, Daniel Valley, Dana R. Blanski, Alex Jewell, Scott Moore, Helen Betsou, Fay |
author_facet | Ammerlaan, Wim Trouet, Johanna Sachs, Michael C. Guan, Ping Carithers, Latarsha Lambert, Pauline Frasquilho, Sonia Antunes, Laurent Kofanova, Olga Rohrer, Daniel Valley, Dana R. Blanski, Alex Jewell, Scott Moore, Helen Betsou, Fay |
author_sort | Ammerlaan, Wim |
collection | PubMed |
description | Although there are millions of formalin-fixed paraffin-embedded (FFPE) tissue blocks potentially available for scientific research, many are of questionable quality, partly due to unknown fixation conditions. We analyzed FFPE tissue biospecimens as part of the NCI Biospecimen Preanalytical Variables (BPV) program to identify microRNA (miRNA) markers for fixation time. miRNA was extracted from kidney and ovary tumor FFPE blocks (19 patients, cold ischemia ≤2 hours) with 6, 12, 24, and 72 hours fixation times, then analyzed using the WaferGen SmartChip platform (miRNA chip with 1036 miRNA targets). For fixation time, principal component analysis of miRNA chip expression data separated 72 hours fixed samples from 6 to 24 hours fixed samples. A set of small nuclear RNA (snRNA) targets was identified that best determines fixation time and was validated using a second independent cohort of seven different tissue types. A customized assay was then developed, based on a set of 24 miRNA and snRNA targets, and a simple “snoRNA score” defined. This score detects FFPE tissue samples with fixation for 72 hours or more, with 79% sensitivity and 80% specificity. It can therefore be used to assess the fitness-for-purpose of FFPE samples for DNA or RNA-based research or clinical assays, which are known to be of limited robustness to formalin overfixation. |
format | Online Article Text |
id | pubmed-6308291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-63082912018-12-28 Small Nucleolar RNA Score: An Assay to Detect Formalin-Overfixed Tissue Ammerlaan, Wim Trouet, Johanna Sachs, Michael C. Guan, Ping Carithers, Latarsha Lambert, Pauline Frasquilho, Sonia Antunes, Laurent Kofanova, Olga Rohrer, Daniel Valley, Dana R. Blanski, Alex Jewell, Scott Moore, Helen Betsou, Fay Biopreserv Biobank Original Articles Although there are millions of formalin-fixed paraffin-embedded (FFPE) tissue blocks potentially available for scientific research, many are of questionable quality, partly due to unknown fixation conditions. We analyzed FFPE tissue biospecimens as part of the NCI Biospecimen Preanalytical Variables (BPV) program to identify microRNA (miRNA) markers for fixation time. miRNA was extracted from kidney and ovary tumor FFPE blocks (19 patients, cold ischemia ≤2 hours) with 6, 12, 24, and 72 hours fixation times, then analyzed using the WaferGen SmartChip platform (miRNA chip with 1036 miRNA targets). For fixation time, principal component analysis of miRNA chip expression data separated 72 hours fixed samples from 6 to 24 hours fixed samples. A set of small nuclear RNA (snRNA) targets was identified that best determines fixation time and was validated using a second independent cohort of seven different tissue types. A customized assay was then developed, based on a set of 24 miRNA and snRNA targets, and a simple “snoRNA score” defined. This score detects FFPE tissue samples with fixation for 72 hours or more, with 79% sensitivity and 80% specificity. It can therefore be used to assess the fitness-for-purpose of FFPE samples for DNA or RNA-based research or clinical assays, which are known to be of limited robustness to formalin overfixation. Mary Ann Liebert, Inc., publishers 2018-12-01 2018-12-17 /pmc/articles/PMC6308291/ /pubmed/30234371 http://dx.doi.org/10.1089/bio.2018.0042 Text en © Wim Ammerlaan et al., 2018; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited. |
spellingShingle | Original Articles Ammerlaan, Wim Trouet, Johanna Sachs, Michael C. Guan, Ping Carithers, Latarsha Lambert, Pauline Frasquilho, Sonia Antunes, Laurent Kofanova, Olga Rohrer, Daniel Valley, Dana R. Blanski, Alex Jewell, Scott Moore, Helen Betsou, Fay Small Nucleolar RNA Score: An Assay to Detect Formalin-Overfixed Tissue |
title | Small Nucleolar RNA Score: An Assay to Detect Formalin-Overfixed Tissue |
title_full | Small Nucleolar RNA Score: An Assay to Detect Formalin-Overfixed Tissue |
title_fullStr | Small Nucleolar RNA Score: An Assay to Detect Formalin-Overfixed Tissue |
title_full_unstemmed | Small Nucleolar RNA Score: An Assay to Detect Formalin-Overfixed Tissue |
title_short | Small Nucleolar RNA Score: An Assay to Detect Formalin-Overfixed Tissue |
title_sort | small nucleolar rna score: an assay to detect formalin-overfixed tissue |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308291/ https://www.ncbi.nlm.nih.gov/pubmed/30234371 http://dx.doi.org/10.1089/bio.2018.0042 |
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