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A model for the impact of FFPE section thickness on gene copy number measurement by FISH
Fluorescent in situ hybridization (FISH) assays to detect gene amplification such as HER2 or MET in tumors are used for prognosis evaluation and selection of targeted therapies. Although FISH guidelines recommended 4~6 μm FFPE sections, many laboratories use 2~3 μm sections, which is a common practi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525178/ https://www.ncbi.nlm.nih.gov/pubmed/31101839 http://dx.doi.org/10.1038/s41598-019-44015-7 |
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author | Yu, Jiyan Wang, Qi Xue, Pu Zheng, Li Mo, Juanfen Chen, Liangye Yin, Manxiang Huang, Yueyan Bao, Yi Ding, Feng |
author_facet | Yu, Jiyan Wang, Qi Xue, Pu Zheng, Li Mo, Juanfen Chen, Liangye Yin, Manxiang Huang, Yueyan Bao, Yi Ding, Feng |
author_sort | Yu, Jiyan |
collection | PubMed |
description | Fluorescent in situ hybridization (FISH) assays to detect gene amplification such as HER2 or MET in tumors are used for prognosis evaluation and selection of targeted therapies. Although FISH guidelines recommended 4~6 μm FFPE sections, many laboratories use 2~3 μm sections, which is a common practice for H&E staining and immunohistochemistry. A former study concluded that section thickness did not affect FISH results. We found, however, that thinner FFPE sections may lead to false negative results for gene amplification. A mathematic model was constructed and cell-line based controls with known gene copy number were prepared, and the model had a reasonable fit with the experimental data. The model revealed that even when counting the apparently full-sized nuclear images, many of them have partial volumes, which leads to under-estimation of gene copy number. Therefore, improperly thinner sections are prone to give false negative results, and thicker sections give a better approximation to the true value. The discrepancy between this and the former study was discussed. In summary, the model applies generally to FISH/ISH detection of gene copy number, and section thickness is an important parameter to control for precision medicine research, assay development, clinical trials and daily practice in pathology laboratory. |
format | Online Article Text |
id | pubmed-6525178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65251782019-05-29 A model for the impact of FFPE section thickness on gene copy number measurement by FISH Yu, Jiyan Wang, Qi Xue, Pu Zheng, Li Mo, Juanfen Chen, Liangye Yin, Manxiang Huang, Yueyan Bao, Yi Ding, Feng Sci Rep Article Fluorescent in situ hybridization (FISH) assays to detect gene amplification such as HER2 or MET in tumors are used for prognosis evaluation and selection of targeted therapies. Although FISH guidelines recommended 4~6 μm FFPE sections, many laboratories use 2~3 μm sections, which is a common practice for H&E staining and immunohistochemistry. A former study concluded that section thickness did not affect FISH results. We found, however, that thinner FFPE sections may lead to false negative results for gene amplification. A mathematic model was constructed and cell-line based controls with known gene copy number were prepared, and the model had a reasonable fit with the experimental data. The model revealed that even when counting the apparently full-sized nuclear images, many of them have partial volumes, which leads to under-estimation of gene copy number. Therefore, improperly thinner sections are prone to give false negative results, and thicker sections give a better approximation to the true value. The discrepancy between this and the former study was discussed. In summary, the model applies generally to FISH/ISH detection of gene copy number, and section thickness is an important parameter to control for precision medicine research, assay development, clinical trials and daily practice in pathology laboratory. Nature Publishing Group UK 2019-05-17 /pmc/articles/PMC6525178/ /pubmed/31101839 http://dx.doi.org/10.1038/s41598-019-44015-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yu, Jiyan Wang, Qi Xue, Pu Zheng, Li Mo, Juanfen Chen, Liangye Yin, Manxiang Huang, Yueyan Bao, Yi Ding, Feng A model for the impact of FFPE section thickness on gene copy number measurement by FISH |
title | A model for the impact of FFPE section thickness on gene copy number measurement by FISH |
title_full | A model for the impact of FFPE section thickness on gene copy number measurement by FISH |
title_fullStr | A model for the impact of FFPE section thickness on gene copy number measurement by FISH |
title_full_unstemmed | A model for the impact of FFPE section thickness on gene copy number measurement by FISH |
title_short | A model for the impact of FFPE section thickness on gene copy number measurement by FISH |
title_sort | model for the impact of ffpe section thickness on gene copy number measurement by fish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525178/ https://www.ncbi.nlm.nih.gov/pubmed/31101839 http://dx.doi.org/10.1038/s41598-019-44015-7 |
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