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Gene Expression Analysis of Aggressive Clinical T1 Stage Clear Cell Renal Cell Carcinoma for Identifying Potential Diagnostic and Prognostic Biomarkers

Authors
 Park, Jee Soo  ;  Pierorazio, Phillip M.  ;  Lee, Ji Hyun  ;  Lee, Hyo Jung  ;  Lim, Young Soun  ;  Jang, Won Sik  ;  Kim, Jongchan  ;  Lee, Seung Hwan  ;  Rha, Koon Ho  ;  Cho, Nam Hoon  ;  Ham, Won Sik 
Citation
 CANCERS, Vol.12(1), 2020-01 
Article Number
 222 
Journal Title
CANCERS
ISSN
 2072-6694 
Issue Date
2020-01
Keywords
SYNCHRONOUS METASTASIS ; SURVIVAL ; BAP1 ; MUTATIONS ; STRINGTIE ; SETD2 ; HISAT ; TOOL
Keywords
clear cell renal cell carcinomas ; RNA sequencing ; gene expression analysis ; prognostic biomarkers
Abstract
The molecular characteristics of early-stage clear cell renal cell carcinomas (ccRCCs) measuring <= 7 cm associated with poor clinical outcomes remain poorly understood. Here, we sought to validate genes associated with ccRCC progression and identify candidate genes to predict ccRCC aggressiveness. From among 1069 nephrectomies performed on patients, RNA sequencing was performed for 12 ccRCC patients with aggressive characteristics and matched pairs of 12 ccRCC patients without aggressive characteristics. Using a prospective cohort (ClinicalTrials.gov Identifier: NCT03694912), the expression levels of nine genes (PBRM1, BAP1, SETD2, KDM5C, FOXC2, CLIP4, AQP1, DDX11, and BAIAP2L1) were measured by reverse-transcription polymerase chain reaction from frozen tissues, and their relation to Fuhrman grade was investigated in 70 patients with small ccRCC (<= 4 cm). In total, 251 genes were differentially expressed and presented fold changes with p-values < 0.05; moreover, 10 genes with the greatest upregulation or downregulation in aggressive ccRCC remained significant even after adjustment. We validated previously identified genes that were associated with ccRCC progression and identified new candidate genes that reflected the aggressiveness of ccRCC. Our study provides new insight into the tumor biology of ccRCC and will help stratify patients with early-stage ccRCC by molecular subtyping.
DOI
10.3390/cancers12010222
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Urology (비뇨의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Jong Chan(김종찬) ORCID logo https://orcid.org/0000-0002-0022-6689
Rha, Koon Ho(나군호) ORCID logo https://orcid.org/0000-0001-8588-7584
Lee, Seung Hwan(이승환) ORCID logo https://orcid.org/0000-0001-7358-8544
Jang, Won Sik(장원식) ORCID logo https://orcid.org/0000-0002-9082-0381
Cho, Nam Hoon(조남훈) ORCID logo https://orcid.org/0000-0002-0045-6441
Ham, Won Sik(함원식) ORCID logo https://orcid.org/0000-0003-2246-8838
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/175240
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