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Roadmap to Local Tumour Growth: Insights from Cervical Cancer

Wide tumour excision is currently the standard approach to surgical treatment of solid cancers including carcinomas of the lower genital tract. This strategy is based on the premise that tumours exhibit isotropic growth potential. We reviewed and analysed local tumour spreading patterns in 518 patie...

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Autores principales: Kubitschke, Hans, Wolf, Benjamin, Morawetz, Erik, Horn, Lars-Christian, Aktas, Bahriye, Behn, Ulrich, Höckel, Michael, Käs, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6726627/
https://www.ncbi.nlm.nih.gov/pubmed/31484955
http://dx.doi.org/10.1038/s41598-019-49182-1
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author Kubitschke, Hans
Wolf, Benjamin
Morawetz, Erik
Horn, Lars-Christian
Aktas, Bahriye
Behn, Ulrich
Höckel, Michael
Käs, Josef
author_facet Kubitschke, Hans
Wolf, Benjamin
Morawetz, Erik
Horn, Lars-Christian
Aktas, Bahriye
Behn, Ulrich
Höckel, Michael
Käs, Josef
author_sort Kubitschke, Hans
collection PubMed
description Wide tumour excision is currently the standard approach to surgical treatment of solid cancers including carcinomas of the lower genital tract. This strategy is based on the premise that tumours exhibit isotropic growth potential. We reviewed and analysed local tumour spreading patterns in 518 patients with cancer of the uterine cervix who underwent surgical tumour resection. Based on data obtained from pathological examination of the surgical specimen, we applied computational modelling techniques to simulate local tumour spread in order to identify parameters influencing preferred infiltration patterns and used area-proportional Euler diagrams to detect and confirm ordered patterns of tumour spread. Some anatomical structures, e.g. tissues of the urinary bladder, were significantly more likely to be infiltrated than other structures, e.g. the ureter and the rectum. Computational models assuming isotropic growth could not explain these infiltration patterns. Introducing ontogenetic distance of a tissue relative to the uterine cervix as a parameter led to accurate predictions of the clinically observed infiltration likelihoods. The clinical data indicates that successive infiltration likelihoods of ontogenetically distant tissues are nearly perfect subsets of ontogenetically closer tissues. The prevailing assumption of isotropic tumour extension has significant shortcomings in the case of cervical cancer. Rather, cervical cancer spread seems to follow ontogenetically defined trajectories.
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spelling pubmed-67266272019-09-18 Roadmap to Local Tumour Growth: Insights from Cervical Cancer Kubitschke, Hans Wolf, Benjamin Morawetz, Erik Horn, Lars-Christian Aktas, Bahriye Behn, Ulrich Höckel, Michael Käs, Josef Sci Rep Article Wide tumour excision is currently the standard approach to surgical treatment of solid cancers including carcinomas of the lower genital tract. This strategy is based on the premise that tumours exhibit isotropic growth potential. We reviewed and analysed local tumour spreading patterns in 518 patients with cancer of the uterine cervix who underwent surgical tumour resection. Based on data obtained from pathological examination of the surgical specimen, we applied computational modelling techniques to simulate local tumour spread in order to identify parameters influencing preferred infiltration patterns and used area-proportional Euler diagrams to detect and confirm ordered patterns of tumour spread. Some anatomical structures, e.g. tissues of the urinary bladder, were significantly more likely to be infiltrated than other structures, e.g. the ureter and the rectum. Computational models assuming isotropic growth could not explain these infiltration patterns. Introducing ontogenetic distance of a tissue relative to the uterine cervix as a parameter led to accurate predictions of the clinically observed infiltration likelihoods. The clinical data indicates that successive infiltration likelihoods of ontogenetically distant tissues are nearly perfect subsets of ontogenetically closer tissues. The prevailing assumption of isotropic tumour extension has significant shortcomings in the case of cervical cancer. Rather, cervical cancer spread seems to follow ontogenetically defined trajectories. Nature Publishing Group UK 2019-09-04 /pmc/articles/PMC6726627/ /pubmed/31484955 http://dx.doi.org/10.1038/s41598-019-49182-1 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
Kubitschke, Hans
Wolf, Benjamin
Morawetz, Erik
Horn, Lars-Christian
Aktas, Bahriye
Behn, Ulrich
Höckel, Michael
Käs, Josef
Roadmap to Local Tumour Growth: Insights from Cervical Cancer
title Roadmap to Local Tumour Growth: Insights from Cervical Cancer
title_full Roadmap to Local Tumour Growth: Insights from Cervical Cancer
title_fullStr Roadmap to Local Tumour Growth: Insights from Cervical Cancer
title_full_unstemmed Roadmap to Local Tumour Growth: Insights from Cervical Cancer
title_short Roadmap to Local Tumour Growth: Insights from Cervical Cancer
title_sort roadmap to local tumour growth: insights from cervical cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6726627/
https://www.ncbi.nlm.nih.gov/pubmed/31484955
http://dx.doi.org/10.1038/s41598-019-49182-1
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