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Quantitative assessment of the relationship between RASSF1A gene promoter methylation and bladder cancer (PRISMA)

BACKGROUND: Methylation of the Ras-association domain family 1 isoform A (RASSF1A) gene promoter region is thought to participate in the initiation and development of many different cancers. However, in bladder cancer the role of RASSF1A methylation was unclear. To evaluate the relationship between...

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Autores principales: Zhan, Leyun, Zhang, Bingyi, Tan, Yaojun, Yang, Chengliang, Huang, Chenhong, Wu, Qiongya, Zhang, Yulin, Chen, Xiaobo, Zhou, Mi, Shu, Aihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319510/
https://www.ncbi.nlm.nih.gov/pubmed/28207521
http://dx.doi.org/10.1097/MD.0000000000006097
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author Zhan, Leyun
Zhang, Bingyi
Tan, Yaojun
Yang, Chengliang
Huang, Chenhong
Wu, Qiongya
Zhang, Yulin
Chen, Xiaobo
Zhou, Mi
Shu, Aihua
author_facet Zhan, Leyun
Zhang, Bingyi
Tan, Yaojun
Yang, Chengliang
Huang, Chenhong
Wu, Qiongya
Zhang, Yulin
Chen, Xiaobo
Zhou, Mi
Shu, Aihua
author_sort Zhan, Leyun
collection PubMed
description BACKGROUND: Methylation of the Ras-association domain family 1 isoform A (RASSF1A) gene promoter region is thought to participate in the initiation and development of many different cancers. However, in bladder cancer the role of RASSF1A methylation was unclear. To evaluate the relationship between RASSF1A methylation and bladder cancer, a quantitative assessment of an independent meta-analysis was performed. In addition, a DNA methylation microarray database from the cancer genome atlas (TCGA) project was used to validate the results of the meta-analysis. METHODS: We searched published articles from computerized databases, and DNA methylation data were extracted from TCGA project. All data were analyzed by R software. RESULTS: The results of the meta-analysis indicated that the frequency of RASSF1A gene methylation in bladder cancer patients is significantly higher than in healthy controls. The hazard ratio (HR) was 2.24 (95% CI = [1.45; 3.48], P = 0.0003) for overall survival (OS), and the RASSF1A gene promoter methylation status was strongly associated with the TNM stage and differentiation grade of the tumor. The similar results were also found by the data from TCGA project. CONCLUSION: There was a significant relationship between the methylation of the RASSF1A gene promoter and bladder cancer. Therefore, RASSF1A gene promoter methylation will be a potential biomarker for the clinical diagnosis of bladder cancer.
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spelling pubmed-53195102017-03-02 Quantitative assessment of the relationship between RASSF1A gene promoter methylation and bladder cancer (PRISMA) Zhan, Leyun Zhang, Bingyi Tan, Yaojun Yang, Chengliang Huang, Chenhong Wu, Qiongya Zhang, Yulin Chen, Xiaobo Zhou, Mi Shu, Aihua Medicine (Baltimore) 5700 BACKGROUND: Methylation of the Ras-association domain family 1 isoform A (RASSF1A) gene promoter region is thought to participate in the initiation and development of many different cancers. However, in bladder cancer the role of RASSF1A methylation was unclear. To evaluate the relationship between RASSF1A methylation and bladder cancer, a quantitative assessment of an independent meta-analysis was performed. In addition, a DNA methylation microarray database from the cancer genome atlas (TCGA) project was used to validate the results of the meta-analysis. METHODS: We searched published articles from computerized databases, and DNA methylation data were extracted from TCGA project. All data were analyzed by R software. RESULTS: The results of the meta-analysis indicated that the frequency of RASSF1A gene methylation in bladder cancer patients is significantly higher than in healthy controls. The hazard ratio (HR) was 2.24 (95% CI = [1.45; 3.48], P = 0.0003) for overall survival (OS), and the RASSF1A gene promoter methylation status was strongly associated with the TNM stage and differentiation grade of the tumor. The similar results were also found by the data from TCGA project. CONCLUSION: There was a significant relationship between the methylation of the RASSF1A gene promoter and bladder cancer. Therefore, RASSF1A gene promoter methylation will be a potential biomarker for the clinical diagnosis of bladder cancer. Wolters Kluwer Health 2017-02-17 /pmc/articles/PMC5319510/ /pubmed/28207521 http://dx.doi.org/10.1097/MD.0000000000006097 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle 5700
Zhan, Leyun
Zhang, Bingyi
Tan, Yaojun
Yang, Chengliang
Huang, Chenhong
Wu, Qiongya
Zhang, Yulin
Chen, Xiaobo
Zhou, Mi
Shu, Aihua
Quantitative assessment of the relationship between RASSF1A gene promoter methylation and bladder cancer (PRISMA)
title Quantitative assessment of the relationship between RASSF1A gene promoter methylation and bladder cancer (PRISMA)
title_full Quantitative assessment of the relationship between RASSF1A gene promoter methylation and bladder cancer (PRISMA)
title_fullStr Quantitative assessment of the relationship between RASSF1A gene promoter methylation and bladder cancer (PRISMA)
title_full_unstemmed Quantitative assessment of the relationship between RASSF1A gene promoter methylation and bladder cancer (PRISMA)
title_short Quantitative assessment of the relationship between RASSF1A gene promoter methylation and bladder cancer (PRISMA)
title_sort quantitative assessment of the relationship between rassf1a gene promoter methylation and bladder cancer (prisma)
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319510/
https://www.ncbi.nlm.nih.gov/pubmed/28207521
http://dx.doi.org/10.1097/MD.0000000000006097
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