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Deep Learning-Based Multi-Omics Integration Robustly Predicts Relapse in Prostate Cancer

OBJECTIVE: Post-operative biochemical relapse (BCR) continues to occur in a significant percentage of patients with localized prostate cancer (PCa). Current stratification methods are not adequate to identify high-risk patients. The present study exploits the ability of deep learning (DL) algorithms...

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Autores principales: Wei, Ziwei, Han, Dunsheng, Zhang, Cong, Wang, Shiyu, Liu, Jinke, Chao, Fan, Song, Zhenyu, Chen, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259796/
https://www.ncbi.nlm.nih.gov/pubmed/35814412
http://dx.doi.org/10.3389/fonc.2022.893424
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author Wei, Ziwei
Han, Dunsheng
Zhang, Cong
Wang, Shiyu
Liu, Jinke
Chao, Fan
Song, Zhenyu
Chen, Gang
author_facet Wei, Ziwei
Han, Dunsheng
Zhang, Cong
Wang, Shiyu
Liu, Jinke
Chao, Fan
Song, Zhenyu
Chen, Gang
author_sort Wei, Ziwei
collection PubMed
description OBJECTIVE: Post-operative biochemical relapse (BCR) continues to occur in a significant percentage of patients with localized prostate cancer (PCa). Current stratification methods are not adequate to identify high-risk patients. The present study exploits the ability of deep learning (DL) algorithms using the H2O package to combine multi-omics data to resolve this problem. METHODS: Five-omics data from 417 PCa patients from The Cancer Genome Atlas (TCGA) were used to construct the DL-based, relapse-sensitive model. Among them, 265 (63.5%) individuals experienced BCR. Five additional independent validation sets were applied to assess its predictive robustness. Bioinformatics analyses of two relapse-associated subgroups were then performed for identification of differentially expressed genes (DEGs), enriched pathway analysis, copy number analysis and immune cell infiltration analysis. RESULTS: The DL-based model, with a significant difference (P = 6e-9) between two subgroups and good concordance index (C-index = 0.767), were proven to be robust by external validation. 1530 DEGs including 678 up- and 852 down-regulated genes were identified in the high-risk subgroup S2 compared with the low-risk subgroup S1. Enrichment analyses found five hallmark gene sets were up-regulated while 13 were down-regulated. Then, we found that DNA damage repair pathways were significantly enriched in the S2 subgroup. CNV analysis showed that 30.18% of genes were significantly up-regulated and gene amplification on chromosomes 7 and 8 was significantly elevated in the S2 subgroup. Moreover, enrichment analysis revealed that some DEGs and pathways were associated with immunity. Three tumor-infiltrating immune cell (TIIC) groups with a higher proportion in the S2 subgroup (p = 1e-05, p = 8.7e-06, p = 0.00014) and one TIIC group with a higher proportion in the S1 subgroup (P = 1.3e-06) were identified. CONCLUSION: We developed a novel, robust classification for understanding PCa relapse. This study validated the effectiveness of deep learning technique in prognosis prediction, and the method may benefit patients and prevent relapse by improving early detection and advancing early intervention.
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spelling pubmed-92597962022-07-08 Deep Learning-Based Multi-Omics Integration Robustly Predicts Relapse in Prostate Cancer Wei, Ziwei Han, Dunsheng Zhang, Cong Wang, Shiyu Liu, Jinke Chao, Fan Song, Zhenyu Chen, Gang Front Oncol Oncology OBJECTIVE: Post-operative biochemical relapse (BCR) continues to occur in a significant percentage of patients with localized prostate cancer (PCa). Current stratification methods are not adequate to identify high-risk patients. The present study exploits the ability of deep learning (DL) algorithms using the H2O package to combine multi-omics data to resolve this problem. METHODS: Five-omics data from 417 PCa patients from The Cancer Genome Atlas (TCGA) were used to construct the DL-based, relapse-sensitive model. Among them, 265 (63.5%) individuals experienced BCR. Five additional independent validation sets were applied to assess its predictive robustness. Bioinformatics analyses of two relapse-associated subgroups were then performed for identification of differentially expressed genes (DEGs), enriched pathway analysis, copy number analysis and immune cell infiltration analysis. RESULTS: The DL-based model, with a significant difference (P = 6e-9) between two subgroups and good concordance index (C-index = 0.767), were proven to be robust by external validation. 1530 DEGs including 678 up- and 852 down-regulated genes were identified in the high-risk subgroup S2 compared with the low-risk subgroup S1. Enrichment analyses found five hallmark gene sets were up-regulated while 13 were down-regulated. Then, we found that DNA damage repair pathways were significantly enriched in the S2 subgroup. CNV analysis showed that 30.18% of genes were significantly up-regulated and gene amplification on chromosomes 7 and 8 was significantly elevated in the S2 subgroup. Moreover, enrichment analysis revealed that some DEGs and pathways were associated with immunity. Three tumor-infiltrating immune cell (TIIC) groups with a higher proportion in the S2 subgroup (p = 1e-05, p = 8.7e-06, p = 0.00014) and one TIIC group with a higher proportion in the S1 subgroup (P = 1.3e-06) were identified. CONCLUSION: We developed a novel, robust classification for understanding PCa relapse. This study validated the effectiveness of deep learning technique in prognosis prediction, and the method may benefit patients and prevent relapse by improving early detection and advancing early intervention. Frontiers Media S.A. 2022-06-23 /pmc/articles/PMC9259796/ /pubmed/35814412 http://dx.doi.org/10.3389/fonc.2022.893424 Text en Copyright © 2022 Wei, Han, Zhang, Wang, Liu, Chao, Song and Chen 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 Oncology
Wei, Ziwei
Han, Dunsheng
Zhang, Cong
Wang, Shiyu
Liu, Jinke
Chao, Fan
Song, Zhenyu
Chen, Gang
Deep Learning-Based Multi-Omics Integration Robustly Predicts Relapse in Prostate Cancer
title Deep Learning-Based Multi-Omics Integration Robustly Predicts Relapse in Prostate Cancer
title_full Deep Learning-Based Multi-Omics Integration Robustly Predicts Relapse in Prostate Cancer
title_fullStr Deep Learning-Based Multi-Omics Integration Robustly Predicts Relapse in Prostate Cancer
title_full_unstemmed Deep Learning-Based Multi-Omics Integration Robustly Predicts Relapse in Prostate Cancer
title_short Deep Learning-Based Multi-Omics Integration Robustly Predicts Relapse in Prostate Cancer
title_sort deep learning-based multi-omics integration robustly predicts relapse in prostate cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259796/
https://www.ncbi.nlm.nih.gov/pubmed/35814412
http://dx.doi.org/10.3389/fonc.2022.893424
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