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3D Shape Modeling for Cell Nuclear Morphological Analysis and Classification
Quantitative analysis of morphological changes in a cell nucleus is important for the understanding of nuclear architecture and its relationship with pathological conditions such as cancer. However, dimensionality of imaging data, together with a great variability of nuclear shapes, presents challen...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135819/ https://www.ncbi.nlm.nih.gov/pubmed/30209281 http://dx.doi.org/10.1038/s41598-018-31924-2 |
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author | Kalinin, Alexandr A. Allyn-Feuer, Ari Ade, Alex Fon, Gordon-Victor Meixner, Walter Dilworth, David Husain, Syed S. de Wet, Jeffrey R. Higgins, Gerald A. Zheng, Gen Creekmore, Amy Wiley, John W. Verdone, James E. Veltri, Robert W. Pienta, Kenneth J. Coffey, Donald S. Athey, Brian D. Dinov, Ivo D. |
author_facet | Kalinin, Alexandr A. Allyn-Feuer, Ari Ade, Alex Fon, Gordon-Victor Meixner, Walter Dilworth, David Husain, Syed S. de Wet, Jeffrey R. Higgins, Gerald A. Zheng, Gen Creekmore, Amy Wiley, John W. Verdone, James E. Veltri, Robert W. Pienta, Kenneth J. Coffey, Donald S. Athey, Brian D. Dinov, Ivo D. |
author_sort | Kalinin, Alexandr A. |
collection | PubMed |
description | Quantitative analysis of morphological changes in a cell nucleus is important for the understanding of nuclear architecture and its relationship with pathological conditions such as cancer. However, dimensionality of imaging data, together with a great variability of nuclear shapes, presents challenges for 3D morphological analysis. Thus, there is a compelling need for robust 3D nuclear morphometric techniques to carry out population-wide analysis. We propose a new approach that combines modeling, analysis, and interpretation of morphometric characteristics of cell nuclei and nucleoli in 3D. We used robust surface reconstruction that allows accurate approximation of 3D object boundary. Then, we computed geometric morphological measures characterizing the form of cell nuclei and nucleoli. Using these features, we compared over 450 nuclei with about 1,000 nucleoli of epithelial and mesenchymal prostate cancer cells, as well as 1,000 nuclei with over 2,000 nucleoli from serum-starved and proliferating fibroblast cells. Classification of sets of 9 and 15 cells achieved accuracy of 95.4% and 98%, respectively, for prostate cancer cells, and 95% and 98% for fibroblast cells. To our knowledge, this is the first attempt to combine these methods for 3D nuclear shape modeling and morphometry into a highly parallel pipeline workflow for morphometric analysis of thousands of nuclei and nucleoli in 3D. |
format | Online Article Text |
id | pubmed-6135819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61358192018-09-15 3D Shape Modeling for Cell Nuclear Morphological Analysis and Classification Kalinin, Alexandr A. Allyn-Feuer, Ari Ade, Alex Fon, Gordon-Victor Meixner, Walter Dilworth, David Husain, Syed S. de Wet, Jeffrey R. Higgins, Gerald A. Zheng, Gen Creekmore, Amy Wiley, John W. Verdone, James E. Veltri, Robert W. Pienta, Kenneth J. Coffey, Donald S. Athey, Brian D. Dinov, Ivo D. Sci Rep Article Quantitative analysis of morphological changes in a cell nucleus is important for the understanding of nuclear architecture and its relationship with pathological conditions such as cancer. However, dimensionality of imaging data, together with a great variability of nuclear shapes, presents challenges for 3D morphological analysis. Thus, there is a compelling need for robust 3D nuclear morphometric techniques to carry out population-wide analysis. We propose a new approach that combines modeling, analysis, and interpretation of morphometric characteristics of cell nuclei and nucleoli in 3D. We used robust surface reconstruction that allows accurate approximation of 3D object boundary. Then, we computed geometric morphological measures characterizing the form of cell nuclei and nucleoli. Using these features, we compared over 450 nuclei with about 1,000 nucleoli of epithelial and mesenchymal prostate cancer cells, as well as 1,000 nuclei with over 2,000 nucleoli from serum-starved and proliferating fibroblast cells. Classification of sets of 9 and 15 cells achieved accuracy of 95.4% and 98%, respectively, for prostate cancer cells, and 95% and 98% for fibroblast cells. To our knowledge, this is the first attempt to combine these methods for 3D nuclear shape modeling and morphometry into a highly parallel pipeline workflow for morphometric analysis of thousands of nuclei and nucleoli in 3D. Nature Publishing Group UK 2018-09-12 /pmc/articles/PMC6135819/ /pubmed/30209281 http://dx.doi.org/10.1038/s41598-018-31924-2 Text en © The Author(s) 2018 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 Kalinin, Alexandr A. Allyn-Feuer, Ari Ade, Alex Fon, Gordon-Victor Meixner, Walter Dilworth, David Husain, Syed S. de Wet, Jeffrey R. Higgins, Gerald A. Zheng, Gen Creekmore, Amy Wiley, John W. Verdone, James E. Veltri, Robert W. Pienta, Kenneth J. Coffey, Donald S. Athey, Brian D. Dinov, Ivo D. 3D Shape Modeling for Cell Nuclear Morphological Analysis and Classification |
title | 3D Shape Modeling for Cell Nuclear Morphological Analysis and Classification |
title_full | 3D Shape Modeling for Cell Nuclear Morphological Analysis and Classification |
title_fullStr | 3D Shape Modeling for Cell Nuclear Morphological Analysis and Classification |
title_full_unstemmed | 3D Shape Modeling for Cell Nuclear Morphological Analysis and Classification |
title_short | 3D Shape Modeling for Cell Nuclear Morphological Analysis and Classification |
title_sort | 3d shape modeling for cell nuclear morphological analysis and classification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135819/ https://www.ncbi.nlm.nih.gov/pubmed/30209281 http://dx.doi.org/10.1038/s41598-018-31924-2 |
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