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Are we there yet? A machine learning architecture to predict organotropic metastases

BACKGROUND & AIMS: Cancer metastasis into distant organs is an evolutionarily selective process. A better understanding of the driving forces endowing proliferative plasticity of tumor seeds in distant soils is required to develop and adapt better treatment systems for this lethal stage of the d...

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Autores principales: Skaro, Michael, Hill, Marcus, Zhou, Yi, Quinn, Shannon, Davis, Melissa B., Sboner, Andrea, Murph, Mandi, Arnold, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611885/
https://www.ncbi.nlm.nih.gov/pubmed/34819069
http://dx.doi.org/10.1186/s12920-021-01122-7
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author Skaro, Michael
Hill, Marcus
Zhou, Yi
Quinn, Shannon
Davis, Melissa B.
Sboner, Andrea
Murph, Mandi
Arnold, Jonathan
author_facet Skaro, Michael
Hill, Marcus
Zhou, Yi
Quinn, Shannon
Davis, Melissa B.
Sboner, Andrea
Murph, Mandi
Arnold, Jonathan
author_sort Skaro, Michael
collection PubMed
description BACKGROUND & AIMS: Cancer metastasis into distant organs is an evolutionarily selective process. A better understanding of the driving forces endowing proliferative plasticity of tumor seeds in distant soils is required to develop and adapt better treatment systems for this lethal stage of the disease. To this end, we aimed to utilize transcript expression profiling features to predict the site-specific metastases of primary tumors and second, to identify the determinants of tissue specific progression. METHODS: We used statistical machine learning for transcript feature selection to optimize classification and built tree-based classifiers to predict tissue specific sites of metastatic progression. RESULTS: We developed a novel machine learning architecture that analyzes 33 types of RNA transcriptome profiles from The Cancer Genome Atlas (TCGA) database. Our classifier identifies the tumor type, derives synthetic instances of primary tumors metastasizing to distant organs and classifies the site-specific metastases in 16 types of cancers metastasizing to 12 locations. CONCLUSIONS: We have demonstrated that site specific metastatic progression is predictable using transcriptomic profiling data from primary tumors and that the overrepresented biological processes in tumors metastasizing to congruent distant loci are highly overlapping. These results indicate site-specific progression was organotropic and core features of biological signaling pathways are identifiable that may describe proliferative plasticity in distant soils. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-021-01122-7.
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spelling pubmed-86118852021-11-29 Are we there yet? A machine learning architecture to predict organotropic metastases Skaro, Michael Hill, Marcus Zhou, Yi Quinn, Shannon Davis, Melissa B. Sboner, Andrea Murph, Mandi Arnold, Jonathan BMC Med Genomics Technical Advance BACKGROUND & AIMS: Cancer metastasis into distant organs is an evolutionarily selective process. A better understanding of the driving forces endowing proliferative plasticity of tumor seeds in distant soils is required to develop and adapt better treatment systems for this lethal stage of the disease. To this end, we aimed to utilize transcript expression profiling features to predict the site-specific metastases of primary tumors and second, to identify the determinants of tissue specific progression. METHODS: We used statistical machine learning for transcript feature selection to optimize classification and built tree-based classifiers to predict tissue specific sites of metastatic progression. RESULTS: We developed a novel machine learning architecture that analyzes 33 types of RNA transcriptome profiles from The Cancer Genome Atlas (TCGA) database. Our classifier identifies the tumor type, derives synthetic instances of primary tumors metastasizing to distant organs and classifies the site-specific metastases in 16 types of cancers metastasizing to 12 locations. CONCLUSIONS: We have demonstrated that site specific metastatic progression is predictable using transcriptomic profiling data from primary tumors and that the overrepresented biological processes in tumors metastasizing to congruent distant loci are highly overlapping. These results indicate site-specific progression was organotropic and core features of biological signaling pathways are identifiable that may describe proliferative plasticity in distant soils. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-021-01122-7. BioMed Central 2021-11-24 /pmc/articles/PMC8611885/ /pubmed/34819069 http://dx.doi.org/10.1186/s12920-021-01122-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Technical Advance
Skaro, Michael
Hill, Marcus
Zhou, Yi
Quinn, Shannon
Davis, Melissa B.
Sboner, Andrea
Murph, Mandi
Arnold, Jonathan
Are we there yet? A machine learning architecture to predict organotropic metastases
title Are we there yet? A machine learning architecture to predict organotropic metastases
title_full Are we there yet? A machine learning architecture to predict organotropic metastases
title_fullStr Are we there yet? A machine learning architecture to predict organotropic metastases
title_full_unstemmed Are we there yet? A machine learning architecture to predict organotropic metastases
title_short Are we there yet? A machine learning architecture to predict organotropic metastases
title_sort are we there yet? a machine learning architecture to predict organotropic metastases
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611885/
https://www.ncbi.nlm.nih.gov/pubmed/34819069
http://dx.doi.org/10.1186/s12920-021-01122-7
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