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A classification method of gastric cancer subtype based on residual graph convolution network

Background: Clinical diagnosis and treatment of tumors are greatly complicated by their heterogeneity, and the subtype classification of cancer frequently plays a significant role in the subsequent treatment of tumors. Presently, the majority of studies rely far too heavily on gene expression data,...

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Autores principales: Liu, Can, Duan, Yuchen, Zhou, Qingqing, Wang, Yongkang, Gao, Yong, Kan, Hongxing, Hu, Jili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845413/
https://www.ncbi.nlm.nih.gov/pubmed/36685956
http://dx.doi.org/10.3389/fgene.2022.1090394
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author Liu, Can
Duan, Yuchen
Zhou, Qingqing
Wang, Yongkang
Gao, Yong
Kan, Hongxing
Hu, Jili
author_facet Liu, Can
Duan, Yuchen
Zhou, Qingqing
Wang, Yongkang
Gao, Yong
Kan, Hongxing
Hu, Jili
author_sort Liu, Can
collection PubMed
description Background: Clinical diagnosis and treatment of tumors are greatly complicated by their heterogeneity, and the subtype classification of cancer frequently plays a significant role in the subsequent treatment of tumors. Presently, the majority of studies rely far too heavily on gene expression data, omitting the enormous power of multi-omics fusion data and the potential for patient similarities. Method: In this study, we created a gastric cancer subtype classification model called RRGCN based on residual graph convolutional network (GCN) using multi-omics fusion data and patient similarity network. Given the multi-omics data’s high dimensionality, we built an artificial neural network Autoencoder (AE) to reduce the dimensionality of the data and extract hidden layer features. The model is then built using the feature data. In addition, we computed the correlation between patients using the Pearson correlation coefficient, and this relationship between patients forms the edge of the graph structure. Four graph convolutional network layers and two residual networks with skip connections make up RRGCN, which reduces the amount of information lost during transmission between layers and prevents model degradation. Results: The results show that RRGCN significantly outperforms other classification methods with an accuracy as high as 0.87 when compared to four other traditional machine learning methods and deep learning models. Conclusion: In terms of subtype classification, RRGCN excels in all areas and has the potential to offer fresh perspectives on disease mechanisms and disease progression. It has the potential to be used for a broader range of disorders and to aid in clinical diagnosis.
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spelling pubmed-98454132023-01-19 A classification method of gastric cancer subtype based on residual graph convolution network Liu, Can Duan, Yuchen Zhou, Qingqing Wang, Yongkang Gao, Yong Kan, Hongxing Hu, Jili Front Genet Genetics Background: Clinical diagnosis and treatment of tumors are greatly complicated by their heterogeneity, and the subtype classification of cancer frequently plays a significant role in the subsequent treatment of tumors. Presently, the majority of studies rely far too heavily on gene expression data, omitting the enormous power of multi-omics fusion data and the potential for patient similarities. Method: In this study, we created a gastric cancer subtype classification model called RRGCN based on residual graph convolutional network (GCN) using multi-omics fusion data and patient similarity network. Given the multi-omics data’s high dimensionality, we built an artificial neural network Autoencoder (AE) to reduce the dimensionality of the data and extract hidden layer features. The model is then built using the feature data. In addition, we computed the correlation between patients using the Pearson correlation coefficient, and this relationship between patients forms the edge of the graph structure. Four graph convolutional network layers and two residual networks with skip connections make up RRGCN, which reduces the amount of information lost during transmission between layers and prevents model degradation. Results: The results show that RRGCN significantly outperforms other classification methods with an accuracy as high as 0.87 when compared to four other traditional machine learning methods and deep learning models. Conclusion: In terms of subtype classification, RRGCN excels in all areas and has the potential to offer fresh perspectives on disease mechanisms and disease progression. It has the potential to be used for a broader range of disorders and to aid in clinical diagnosis. Frontiers Media S.A. 2023-01-04 /pmc/articles/PMC9845413/ /pubmed/36685956 http://dx.doi.org/10.3389/fgene.2022.1090394 Text en Copyright © 2023 Liu, Duan, Zhou, Wang, Gao, Kan and Hu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Liu, Can
Duan, Yuchen
Zhou, Qingqing
Wang, Yongkang
Gao, Yong
Kan, Hongxing
Hu, Jili
A classification method of gastric cancer subtype based on residual graph convolution network
title A classification method of gastric cancer subtype based on residual graph convolution network
title_full A classification method of gastric cancer subtype based on residual graph convolution network
title_fullStr A classification method of gastric cancer subtype based on residual graph convolution network
title_full_unstemmed A classification method of gastric cancer subtype based on residual graph convolution network
title_short A classification method of gastric cancer subtype based on residual graph convolution network
title_sort classification method of gastric cancer subtype based on residual graph convolution network
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845413/
https://www.ncbi.nlm.nih.gov/pubmed/36685956
http://dx.doi.org/10.3389/fgene.2022.1090394
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