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DNA Extracted from Cytologic Slides Is a Valuable Source for PCR-Based Molecular Tests

INTRODUCTION: DNA extracted from cytologic samples is occasionally used for various molecular tests. The aim of this study was to evaluate DNA extracted from differently prepared cytologic slides that can be used for PCR-based molecular tests. METHODS: For each 23 cases of papillary thyroid carcinom...

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Autores principales: Kwon, Hyo Sum, Shin, Dong Hoon, Kim, So Young, Hwang, Chung Su, Kim, Arhong, Lee, Hyun Jung, Na, JooYoung, Lee, Jung Hee, Kim, Jee Yeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872841/
https://www.ncbi.nlm.nih.gov/pubmed/36455541
http://dx.doi.org/10.1159/000526634
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author Kwon, Hyo Sum
Shin, Dong Hoon
Kim, So Young
Hwang, Chung Su
Kim, Arhong
Lee, Hyun Jung
Na, JooYoung
Lee, Jung Hee
Kim, Jee Yeon
author_facet Kwon, Hyo Sum
Shin, Dong Hoon
Kim, So Young
Hwang, Chung Su
Kim, Arhong
Lee, Hyun Jung
Na, JooYoung
Lee, Jung Hee
Kim, Jee Yeon
author_sort Kwon, Hyo Sum
collection PubMed
description INTRODUCTION: DNA extracted from cytologic samples is occasionally used for various molecular tests. The aim of this study was to evaluate DNA extracted from differently prepared cytologic slides that can be used for PCR-based molecular tests. METHODS: For each 23 cases of papillary thyroid carcinoma or colorectal adenocarcinoma tissues, six touch-imprinted cytological slides were prepared (group 1∼3), and remnant tissues were blocked for FFPE tissue (group 4). Cytologic slides were grouped by preparation methods: air-dried slides (group 1), fixed slides (group 2), and stained slides (group 3). Fixed slides were classified as 95% ethanol fixed (group 2A) and CytoRich Red Preservative solution fixed (group 2B). Stained slides were divided in 3 ways: Giemsa, Pap, and H&E stained (group 3A, 3B, and 3C, respectively). DNA extracted from each group was evaluated for concentration, 260/280 ratio, DNA Integrity Number (DIN) value, and mutation. RESULTS: DNA concentration was highest in group 1 and lowest in group 2B. DIN value was highest in group 2A and lowest in group 2B. A mutation of BRAF or KRAS genes was detected in 18 FFPE tissue samples. Matched DNA extracts from groups 1, 2A, and 3 produced results consistent with FFPE tissue results, while mutation testing was successful for only four samples of DNA from group 2B. CONCLUSION: The mutation tests worked well for most samples except CytoRich Red Preservative-fixed slides. This study indicates that stained and unstained cytologic slides are a suitable source of PCR-based molecular tests as long as they are fixed in ethanol or stored for a short time in an air-dried condition.
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spelling pubmed-98728412023-01-25 DNA Extracted from Cytologic Slides Is a Valuable Source for PCR-Based Molecular Tests Kwon, Hyo Sum Shin, Dong Hoon Kim, So Young Hwang, Chung Su Kim, Arhong Lee, Hyun Jung Na, JooYoung Lee, Jung Hee Kim, Jee Yeon Acta Cytol Techniques INTRODUCTION: DNA extracted from cytologic samples is occasionally used for various molecular tests. The aim of this study was to evaluate DNA extracted from differently prepared cytologic slides that can be used for PCR-based molecular tests. METHODS: For each 23 cases of papillary thyroid carcinoma or colorectal adenocarcinoma tissues, six touch-imprinted cytological slides were prepared (group 1∼3), and remnant tissues were blocked for FFPE tissue (group 4). Cytologic slides were grouped by preparation methods: air-dried slides (group 1), fixed slides (group 2), and stained slides (group 3). Fixed slides were classified as 95% ethanol fixed (group 2A) and CytoRich Red Preservative solution fixed (group 2B). Stained slides were divided in 3 ways: Giemsa, Pap, and H&E stained (group 3A, 3B, and 3C, respectively). DNA extracted from each group was evaluated for concentration, 260/280 ratio, DNA Integrity Number (DIN) value, and mutation. RESULTS: DNA concentration was highest in group 1 and lowest in group 2B. DIN value was highest in group 2A and lowest in group 2B. A mutation of BRAF or KRAS genes was detected in 18 FFPE tissue samples. Matched DNA extracts from groups 1, 2A, and 3 produced results consistent with FFPE tissue results, while mutation testing was successful for only four samples of DNA from group 2B. CONCLUSION: The mutation tests worked well for most samples except CytoRich Red Preservative-fixed slides. This study indicates that stained and unstained cytologic slides are a suitable source of PCR-based molecular tests as long as they are fixed in ethanol or stored for a short time in an air-dried condition. S. Karger AG 2023-01 2022-12-01 /pmc/articles/PMC9872841/ /pubmed/36455541 http://dx.doi.org/10.1159/000526634 Text en Copyright © 2022 by The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC). Usage and distribution for commercial purposes requires written permission.
spellingShingle Techniques
Kwon, Hyo Sum
Shin, Dong Hoon
Kim, So Young
Hwang, Chung Su
Kim, Arhong
Lee, Hyun Jung
Na, JooYoung
Lee, Jung Hee
Kim, Jee Yeon
DNA Extracted from Cytologic Slides Is a Valuable Source for PCR-Based Molecular Tests
title DNA Extracted from Cytologic Slides Is a Valuable Source for PCR-Based Molecular Tests
title_full DNA Extracted from Cytologic Slides Is a Valuable Source for PCR-Based Molecular Tests
title_fullStr DNA Extracted from Cytologic Slides Is a Valuable Source for PCR-Based Molecular Tests
title_full_unstemmed DNA Extracted from Cytologic Slides Is a Valuable Source for PCR-Based Molecular Tests
title_short DNA Extracted from Cytologic Slides Is a Valuable Source for PCR-Based Molecular Tests
title_sort dna extracted from cytologic slides is a valuable source for pcr-based molecular tests
topic Techniques
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872841/
https://www.ncbi.nlm.nih.gov/pubmed/36455541
http://dx.doi.org/10.1159/000526634
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