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Comparing nodal versus bony metastatic spread using tumour phylogenies

The role of lymph node metastases in distant prostate cancer dissemination and lethality is ill defined. Patients with metastases restricted to lymph nodes have a better prognosis than those with distant metastatic spread, suggesting the possibility of distinct aetiologies. To explore this, we trace...

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Autores principales: Mangiola, Stefano, Hong, Matthew K. H., Cmero, Marek, Kurganovs, Natalie, Ryan, Andrew, Costello, Anthony J., Corcoran, Niall M., Macintyre, Geoff, Hovens, Christopher M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031992/
https://www.ncbi.nlm.nih.gov/pubmed/27653089
http://dx.doi.org/10.1038/srep33918
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author Mangiola, Stefano
Hong, Matthew K. H.
Cmero, Marek
Kurganovs, Natalie
Ryan, Andrew
Costello, Anthony J.
Corcoran, Niall M.
Macintyre, Geoff
Hovens, Christopher M.
author_facet Mangiola, Stefano
Hong, Matthew K. H.
Cmero, Marek
Kurganovs, Natalie
Ryan, Andrew
Costello, Anthony J.
Corcoran, Niall M.
Macintyre, Geoff
Hovens, Christopher M.
author_sort Mangiola, Stefano
collection PubMed
description The role of lymph node metastases in distant prostate cancer dissemination and lethality is ill defined. Patients with metastases restricted to lymph nodes have a better prognosis than those with distant metastatic spread, suggesting the possibility of distinct aetiologies. To explore this, we traced patterns of cancer dissemination using tumour phylogenies inferred from genome-wide copy-number profiling of 48 samples across 3 patients with lymph node metastatic disease and 3 patients with osseous metastatic disease. Our results show that metastatic cells in regional lymph nodes originate from evolutionary advanced extraprostatic tumour cells rather than less advanced central tumour cell populations. In contrast, osseous metastases do not exhibit such a constrained developmental lineage, arising from either intra or extraprostatic tumour cell populations, at early and late stages in the evolution of the primary. Collectively, this comparison suggests that lymph node metastases may not be an intermediate developmental step for distant osseous metastases, but rather represent a distinct metastatic lineage.
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spelling pubmed-50319922016-09-29 Comparing nodal versus bony metastatic spread using tumour phylogenies Mangiola, Stefano Hong, Matthew K. H. Cmero, Marek Kurganovs, Natalie Ryan, Andrew Costello, Anthony J. Corcoran, Niall M. Macintyre, Geoff Hovens, Christopher M. Sci Rep Article The role of lymph node metastases in distant prostate cancer dissemination and lethality is ill defined. Patients with metastases restricted to lymph nodes have a better prognosis than those with distant metastatic spread, suggesting the possibility of distinct aetiologies. To explore this, we traced patterns of cancer dissemination using tumour phylogenies inferred from genome-wide copy-number profiling of 48 samples across 3 patients with lymph node metastatic disease and 3 patients with osseous metastatic disease. Our results show that metastatic cells in regional lymph nodes originate from evolutionary advanced extraprostatic tumour cells rather than less advanced central tumour cell populations. In contrast, osseous metastases do not exhibit such a constrained developmental lineage, arising from either intra or extraprostatic tumour cell populations, at early and late stages in the evolution of the primary. Collectively, this comparison suggests that lymph node metastases may not be an intermediate developmental step for distant osseous metastases, but rather represent a distinct metastatic lineage. Nature Publishing Group 2016-09-22 /pmc/articles/PMC5031992/ /pubmed/27653089 http://dx.doi.org/10.1038/srep33918 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Mangiola, Stefano
Hong, Matthew K. H.
Cmero, Marek
Kurganovs, Natalie
Ryan, Andrew
Costello, Anthony J.
Corcoran, Niall M.
Macintyre, Geoff
Hovens, Christopher M.
Comparing nodal versus bony metastatic spread using tumour phylogenies
title Comparing nodal versus bony metastatic spread using tumour phylogenies
title_full Comparing nodal versus bony metastatic spread using tumour phylogenies
title_fullStr Comparing nodal versus bony metastatic spread using tumour phylogenies
title_full_unstemmed Comparing nodal versus bony metastatic spread using tumour phylogenies
title_short Comparing nodal versus bony metastatic spread using tumour phylogenies
title_sort comparing nodal versus bony metastatic spread using tumour phylogenies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031992/
https://www.ncbi.nlm.nih.gov/pubmed/27653089
http://dx.doi.org/10.1038/srep33918
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