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Prediction of tumor location in prostate cancer tissue using a machine learning system on gene expression data
BACKGROUND: Finding the tumor location in the prostate is an essential pathological step for prostate cancer diagnosis and treatment. The location of the tumor – the laterality – can be unilateral (the tumor is affecting one side of the prostate), or bilateral on both sides. Nevertheless, the tumor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068980/ https://www.ncbi.nlm.nih.gov/pubmed/32164523 http://dx.doi.org/10.1186/s12859-020-3345-9 |
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author | Hamzeh, Osama Alkhateeb, Abedalrhman Zheng, Julia Kandalam, Srinath Rueda, Luis |
author_facet | Hamzeh, Osama Alkhateeb, Abedalrhman Zheng, Julia Kandalam, Srinath Rueda, Luis |
author_sort | Hamzeh, Osama |
collection | PubMed |
description | BACKGROUND: Finding the tumor location in the prostate is an essential pathological step for prostate cancer diagnosis and treatment. The location of the tumor – the laterality – can be unilateral (the tumor is affecting one side of the prostate), or bilateral on both sides. Nevertheless, the tumor can be overestimated or underestimated by standard screening methods. In this work, a combination of efficient machine learning methods for feature selection and classification are proposed to analyze gene activity and select them as relevant biomarkers for different laterality samples. RESULTS: A data set that consists of 450 samples was used in this study. The samples were divided into three laterality classes (left, right, bilateral). The aim of this work is to understand the genomic activity in each class and find relevant genes as indicators for each class with nearly 99% accuracy. The system identified groups of differentially expressed genes (RTN1, HLA-DMB, MRI1) that are able to differentiate samples among the three classes. CONCLUSION: The proposed method was able to detect sets of genes that can identify different laterality classes. The resulting genes are found to be strongly correlated with disease progression. HLA-DMB and EIF4G2, which are detected in the set of genes can detect the left laterality, were reported earlier to be in the same pathway called Allograft rejection SuperPath. |
format | Online Article Text |
id | pubmed-7068980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70689802020-03-18 Prediction of tumor location in prostate cancer tissue using a machine learning system on gene expression data Hamzeh, Osama Alkhateeb, Abedalrhman Zheng, Julia Kandalam, Srinath Rueda, Luis BMC Bioinformatics Research BACKGROUND: Finding the tumor location in the prostate is an essential pathological step for prostate cancer diagnosis and treatment. The location of the tumor – the laterality – can be unilateral (the tumor is affecting one side of the prostate), or bilateral on both sides. Nevertheless, the tumor can be overestimated or underestimated by standard screening methods. In this work, a combination of efficient machine learning methods for feature selection and classification are proposed to analyze gene activity and select them as relevant biomarkers for different laterality samples. RESULTS: A data set that consists of 450 samples was used in this study. The samples were divided into three laterality classes (left, right, bilateral). The aim of this work is to understand the genomic activity in each class and find relevant genes as indicators for each class with nearly 99% accuracy. The system identified groups of differentially expressed genes (RTN1, HLA-DMB, MRI1) that are able to differentiate samples among the three classes. CONCLUSION: The proposed method was able to detect sets of genes that can identify different laterality classes. The resulting genes are found to be strongly correlated with disease progression. HLA-DMB and EIF4G2, which are detected in the set of genes can detect the left laterality, were reported earlier to be in the same pathway called Allograft rejection SuperPath. BioMed Central 2020-03-11 /pmc/articles/PMC7068980/ /pubmed/32164523 http://dx.doi.org/10.1186/s12859-020-3345-9 Text en © The Author(s) 2020 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hamzeh, Osama Alkhateeb, Abedalrhman Zheng, Julia Kandalam, Srinath Rueda, Luis Prediction of tumor location in prostate cancer tissue using a machine learning system on gene expression data |
title | Prediction of tumor location in prostate cancer tissue using a machine learning system on gene expression data |
title_full | Prediction of tumor location in prostate cancer tissue using a machine learning system on gene expression data |
title_fullStr | Prediction of tumor location in prostate cancer tissue using a machine learning system on gene expression data |
title_full_unstemmed | Prediction of tumor location in prostate cancer tissue using a machine learning system on gene expression data |
title_short | Prediction of tumor location in prostate cancer tissue using a machine learning system on gene expression data |
title_sort | prediction of tumor location in prostate cancer tissue using a machine learning system on gene expression data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068980/ https://www.ncbi.nlm.nih.gov/pubmed/32164523 http://dx.doi.org/10.1186/s12859-020-3345-9 |
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