DNA methylation-based classification and identification of bladder cancer prognosis-associated subgroups

Abstract Background Bladder cancer (BCA) is the most common urinary tumor, but its pathogenesis is unclear, and the associated treatment strategy has rarely been updated. In recent years, a deeper understanding of tumor epigenetics has been gained, providing new opportunities for cancer detection an...

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Main Authors: Zijian Tian, Lingfeng Meng, Xingbo Long, Tongxiang Diao, Maolin Hu, Miao Wang, Ming Liu, Jianye Wang
Format: Article
Language:English
Published: BMC 2020-06-01
Series:Cancer Cell International
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12935-020-01345-1
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author Zijian Tian
Lingfeng Meng
Xingbo Long
Tongxiang Diao
Maolin Hu
Miao Wang
Ming Liu
Jianye Wang
author_facet Zijian Tian
Lingfeng Meng
Xingbo Long
Tongxiang Diao
Maolin Hu
Miao Wang
Ming Liu
Jianye Wang
author_sort Zijian Tian
collection DOAJ
description Abstract Background Bladder cancer (BCA) is the most common urinary tumor, but its pathogenesis is unclear, and the associated treatment strategy has rarely been updated. In recent years, a deeper understanding of tumor epigenetics has been gained, providing new opportunities for cancer detection and treatment. Methods We identified prognostic methylation sites based on DNA methylation profiles of BCA in the TCGA database and constructed a specific prognostic subgroup. Results Based on the consistent clustering of 402 CpGs, we identified seven subgroups that had a significant association with survival. The difference in DNA methylation levels was related to T stage, N stage, M stage, grade, sex, age, stage and prognosis. Finally, the prediction model was constructed using a Cox regression model and verified using the test dataset; the prognosis was consistent with that of the training set. Conclusions The classification based on DNA methylation is closely related to the clinicopathological characteristics of BCA and determines the prognostic value of each epigenetic subtype. Therefore, our findings provide a basis for the development of DNA methylation subtype-specific therapeutic strategies for human bladder cancer.
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spelling doaj.art-85fc283777d1435e9d25b0fec072bc732022-12-21T23:57:14ZengBMCCancer Cell International1475-28672020-06-0120111110.1186/s12935-020-01345-1DNA methylation-based classification and identification of bladder cancer prognosis-associated subgroupsZijian Tian0Lingfeng Meng1Xingbo Long2Tongxiang Diao3Maolin Hu4Miao Wang5Ming Liu6Jianye Wang7Department of Urology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical SciencesDepartment of Urology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical SciencesDepartment of Urology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical SciencesDepartment of Urology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical SciencesDepartment of Urology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical SciencesDepartment of Urology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical SciencesDepartment of Urology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical SciencesDepartment of Urology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical SciencesAbstract Background Bladder cancer (BCA) is the most common urinary tumor, but its pathogenesis is unclear, and the associated treatment strategy has rarely been updated. In recent years, a deeper understanding of tumor epigenetics has been gained, providing new opportunities for cancer detection and treatment. Methods We identified prognostic methylation sites based on DNA methylation profiles of BCA in the TCGA database and constructed a specific prognostic subgroup. Results Based on the consistent clustering of 402 CpGs, we identified seven subgroups that had a significant association with survival. The difference in DNA methylation levels was related to T stage, N stage, M stage, grade, sex, age, stage and prognosis. Finally, the prediction model was constructed using a Cox regression model and verified using the test dataset; the prognosis was consistent with that of the training set. Conclusions The classification based on DNA methylation is closely related to the clinicopathological characteristics of BCA and determines the prognostic value of each epigenetic subtype. Therefore, our findings provide a basis for the development of DNA methylation subtype-specific therapeutic strategies for human bladder cancer.http://link.springer.com/article/10.1186/s12935-020-01345-1DNA MethylationUrinary bladder neoplasmsEpigeneticsCluster analysis
spellingShingle Zijian Tian
Lingfeng Meng
Xingbo Long
Tongxiang Diao
Maolin Hu
Miao Wang
Ming Liu
Jianye Wang
DNA methylation-based classification and identification of bladder cancer prognosis-associated subgroups
Cancer Cell International
DNA Methylation
Urinary bladder neoplasms
Epigenetics
Cluster analysis
title DNA methylation-based classification and identification of bladder cancer prognosis-associated subgroups
title_full DNA methylation-based classification and identification of bladder cancer prognosis-associated subgroups
title_fullStr DNA methylation-based classification and identification of bladder cancer prognosis-associated subgroups
title_full_unstemmed DNA methylation-based classification and identification of bladder cancer prognosis-associated subgroups
title_short DNA methylation-based classification and identification of bladder cancer prognosis-associated subgroups
title_sort dna methylation based classification and identification of bladder cancer prognosis associated subgroups
topic DNA Methylation
Urinary bladder neoplasms
Epigenetics
Cluster analysis
url http://link.springer.com/article/10.1186/s12935-020-01345-1
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