In silico DNA methylation analysis identifies potential prognostic biomarkers in type 2 papillary renal cell carcinoma

Abstract There are currently no effective treatments for advanced‐stage papillary renal cell carcinoma (PRCC). The goal of this study is to define potential DNA methylation‐based markers and treatment targets for advanced‐stage type 2 PRCC. Progressive DNA methylation changes and copy number variati...

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Main Authors: Man Yang, Ryan A. Hlady, Dan Zhou, Thai H. Ho, Keith D. Robertson
Format: Article
Language:English
Published: Wiley 2019-09-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.2402
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author Man Yang
Ryan A. Hlady
Dan Zhou
Thai H. Ho
Keith D. Robertson
author_facet Man Yang
Ryan A. Hlady
Dan Zhou
Thai H. Ho
Keith D. Robertson
author_sort Man Yang
collection DOAJ
description Abstract There are currently no effective treatments for advanced‐stage papillary renal cell carcinoma (PRCC). The goal of this study is to define potential DNA methylation‐based markers and treatment targets for advanced‐stage type 2 PRCC. Progressive DNA methylation changes and copy number variation (CNV) from localized to advanced‐stage type 2 PRCC are analyzed by using methylation data generated by TCGA's kidney renal papillary cell carcinoma (TCGA‐KIRP, 450k array) project. Survival analyses are performed for the identified biomarkers and genes with CNV. In addition, expression of the corresponding genes is investigated by RNA‐seq analysis. Progressive methylation changes in several CpGs from localized to advanced‐stage type 2 PRCC are observed. Four CpGs (cg00489401, cg27649239, cg20555674, and cg07196505) in particular are identified as markers for differentiating between localized and advanced‐stage type 2 PRCC. Copy number analysis reveals that copy gain of PTK7 mostly occurs in advanced‐stage type 2 PRCC. Both the four CpG methylation changes and PTK7 copy number gain are associated with patient survival. RNA‐seq analysis demonstrates that PTK7 copy gain leads to higher PTK7 expression relative to tumors without copy number gain. Moreover, PTK7 is significantly upregulated from localized to advanced‐stage type 2 PRCC and is linked to cancer cell invasion. In conclusion, DNA methylation markers that differentiate between localized and advanced‐stage type 2 PRCC may serve as useful markers for disease staging or outcome, while PTK7 copy gain represents a potential treatment target for advanced‐stage type 2 PRCC. Stepwise methylation changes and copy number gain also associate with disease stage in PRCC patients.
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spelling doaj.art-b15879f620204bc092cfdc8e3b6853162022-12-21T19:25:41ZengWileyCancer Medicine2045-76342019-09-018125760576810.1002/cam4.2402In silico DNA methylation analysis identifies potential prognostic biomarkers in type 2 papillary renal cell carcinomaMan Yang0Ryan A. Hlady1Dan Zhou2Thai H. Ho3Keith D. Robertson4Department of Molecular Pharmacology and Experimental Therapeutics Mayo Clinic Rochester MinnesotaDepartment of Molecular Pharmacology and Experimental Therapeutics Mayo Clinic Rochester MinnesotaDepartment of Molecular Pharmacology and Experimental Therapeutics Mayo Clinic Rochester MinnesotaDivision of Hematology and Medical Oncology Mayo Clinic Scottsdale ArizonaDepartment of Molecular Pharmacology and Experimental Therapeutics Mayo Clinic Rochester MinnesotaAbstract There are currently no effective treatments for advanced‐stage papillary renal cell carcinoma (PRCC). The goal of this study is to define potential DNA methylation‐based markers and treatment targets for advanced‐stage type 2 PRCC. Progressive DNA methylation changes and copy number variation (CNV) from localized to advanced‐stage type 2 PRCC are analyzed by using methylation data generated by TCGA's kidney renal papillary cell carcinoma (TCGA‐KIRP, 450k array) project. Survival analyses are performed for the identified biomarkers and genes with CNV. In addition, expression of the corresponding genes is investigated by RNA‐seq analysis. Progressive methylation changes in several CpGs from localized to advanced‐stage type 2 PRCC are observed. Four CpGs (cg00489401, cg27649239, cg20555674, and cg07196505) in particular are identified as markers for differentiating between localized and advanced‐stage type 2 PRCC. Copy number analysis reveals that copy gain of PTK7 mostly occurs in advanced‐stage type 2 PRCC. Both the four CpG methylation changes and PTK7 copy number gain are associated with patient survival. RNA‐seq analysis demonstrates that PTK7 copy gain leads to higher PTK7 expression relative to tumors without copy number gain. Moreover, PTK7 is significantly upregulated from localized to advanced‐stage type 2 PRCC and is linked to cancer cell invasion. In conclusion, DNA methylation markers that differentiate between localized and advanced‐stage type 2 PRCC may serve as useful markers for disease staging or outcome, while PTK7 copy gain represents a potential treatment target for advanced‐stage type 2 PRCC. Stepwise methylation changes and copy number gain also associate with disease stage in PRCC patients.https://doi.org/10.1002/cam4.2402biomarkersepigeneticsepigenomicsgene copy number
spellingShingle Man Yang
Ryan A. Hlady
Dan Zhou
Thai H. Ho
Keith D. Robertson
In silico DNA methylation analysis identifies potential prognostic biomarkers in type 2 papillary renal cell carcinoma
Cancer Medicine
biomarkers
epigenetics
epigenomics
gene copy number
title In silico DNA methylation analysis identifies potential prognostic biomarkers in type 2 papillary renal cell carcinoma
title_full In silico DNA methylation analysis identifies potential prognostic biomarkers in type 2 papillary renal cell carcinoma
title_fullStr In silico DNA methylation analysis identifies potential prognostic biomarkers in type 2 papillary renal cell carcinoma
title_full_unstemmed In silico DNA methylation analysis identifies potential prognostic biomarkers in type 2 papillary renal cell carcinoma
title_short In silico DNA methylation analysis identifies potential prognostic biomarkers in type 2 papillary renal cell carcinoma
title_sort in silico dna methylation analysis identifies potential prognostic biomarkers in type 2 papillary renal cell carcinoma
topic biomarkers
epigenetics
epigenomics
gene copy number
url https://doi.org/10.1002/cam4.2402
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