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

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. Fr...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017065/
https://www.ncbi.nlm.nih.gov/pubmed/31963294
http://dx.doi.org/10.3390/cancers12010222
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author 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
author_facet 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
author_sort Park, Jee Soo
collection PubMed
description 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.
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spelling pubmed-70170652020-02-28 Gene Expression Analysis of Aggressive Clinical T1 Stage Clear Cell Renal Cell Carcinoma for Identifying Potential Diagnostic and Prognostic Biomarkers 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 Cancers (Basel) Article 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. MDPI 2020-01-16 /pmc/articles/PMC7017065/ /pubmed/31963294 http://dx.doi.org/10.3390/cancers12010222 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
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
Gene Expression Analysis of Aggressive Clinical T1 Stage Clear Cell Renal Cell Carcinoma for Identifying Potential Diagnostic and Prognostic Biomarkers
title Gene Expression Analysis of Aggressive Clinical T1 Stage Clear Cell Renal Cell Carcinoma for Identifying Potential Diagnostic and Prognostic Biomarkers
title_full Gene Expression Analysis of Aggressive Clinical T1 Stage Clear Cell Renal Cell Carcinoma for Identifying Potential Diagnostic and Prognostic Biomarkers
title_fullStr Gene Expression Analysis of Aggressive Clinical T1 Stage Clear Cell Renal Cell Carcinoma for Identifying Potential Diagnostic and Prognostic Biomarkers
title_full_unstemmed Gene Expression Analysis of Aggressive Clinical T1 Stage Clear Cell Renal Cell Carcinoma for Identifying Potential Diagnostic and Prognostic Biomarkers
title_short Gene Expression Analysis of Aggressive Clinical T1 Stage Clear Cell Renal Cell Carcinoma for Identifying Potential Diagnostic and Prognostic Biomarkers
title_sort gene expression analysis of aggressive clinical t1 stage clear cell renal cell carcinoma for identifying potential diagnostic and prognostic biomarkers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017065/
https://www.ncbi.nlm.nih.gov/pubmed/31963294
http://dx.doi.org/10.3390/cancers12010222
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