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Whole-transcriptome sequencing identified gene expression signatures associated with aggressive clear cell renal cell carcinoma
Clear cell renal cell carcinoma (ccRCC) is the most prevalent subtype of kidney cancer, yet molecular biomarkers have not been used for the prognosis of ccRCC to aide clinical decision making. This study aimed to identify genes associated with ccRCC aggressiveness and overall survival (OS). Samples...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305109/ https://www.ncbi.nlm.nih.gov/pubmed/30603059 http://dx.doi.org/10.18632/genesandcancer.183 |
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author | Batai, Ken Imler, Elliot Pangilinan, Jayce Bell, Robert Lwin, Aye Price, Elinora Milinic, Tijana Arora, Amit Ellis, Nathan A. Bracamonte, Erika Seligmann, Bruce Lee, Benjamin R. |
author_facet | Batai, Ken Imler, Elliot Pangilinan, Jayce Bell, Robert Lwin, Aye Price, Elinora Milinic, Tijana Arora, Amit Ellis, Nathan A. Bracamonte, Erika Seligmann, Bruce Lee, Benjamin R. |
author_sort | Batai, Ken |
collection | PubMed |
description | Clear cell renal cell carcinoma (ccRCC) is the most prevalent subtype of kidney cancer, yet molecular biomarkers have not been used for the prognosis of ccRCC to aide clinical decision making. This study aimed to identify genes associated with ccRCC aggressiveness and overall survival (OS). Samples of ccRCC tumor tissue were obtained from 33 patients who underwent nephrectomy. Gene expression was determined using whole-transcriptome sequencing. The Cancer Genome Atlas Kidney Renal Clear Cell Carcinoma (TCGA-KIRC) RNA-seq data was used to test association with OS. 290 genes were differentially expressed between tumors with high and low stage, size, grade, and necrosis (SSIGN) score (≥7 vs. ≤3) with P(ADJ)<0.05. Four genes, G6PD, APLP1, GCNT3, and PLPP2, were also over-expressed in advanced stage (III and IV) and high grade (3 and 4) ccRCC and tumor with necrosis (P(ADJ)<0.05). Investigation stratifying by stage found that APLP1 and PLPP2 overexpression were significantly associated with poorer OS in the early stage (Quartile 1 vs. Quartile 4, HR = 3.87, 95% CI:1.25-11.97, P = 0.02 and HR = 4.77, 95% CI:1.37-16.57, P = 0.04 respectively). These genes are potential biomarkers of ccRCC aggressiveness and prognosis that direct clinical and surgical management. |
format | Online Article Text |
id | pubmed-6305109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-63051092019-01-02 Whole-transcriptome sequencing identified gene expression signatures associated with aggressive clear cell renal cell carcinoma Batai, Ken Imler, Elliot Pangilinan, Jayce Bell, Robert Lwin, Aye Price, Elinora Milinic, Tijana Arora, Amit Ellis, Nathan A. Bracamonte, Erika Seligmann, Bruce Lee, Benjamin R. Genes Cancer Research Paper Clear cell renal cell carcinoma (ccRCC) is the most prevalent subtype of kidney cancer, yet molecular biomarkers have not been used for the prognosis of ccRCC to aide clinical decision making. This study aimed to identify genes associated with ccRCC aggressiveness and overall survival (OS). Samples of ccRCC tumor tissue were obtained from 33 patients who underwent nephrectomy. Gene expression was determined using whole-transcriptome sequencing. The Cancer Genome Atlas Kidney Renal Clear Cell Carcinoma (TCGA-KIRC) RNA-seq data was used to test association with OS. 290 genes were differentially expressed between tumors with high and low stage, size, grade, and necrosis (SSIGN) score (≥7 vs. ≤3) with P(ADJ)<0.05. Four genes, G6PD, APLP1, GCNT3, and PLPP2, were also over-expressed in advanced stage (III and IV) and high grade (3 and 4) ccRCC and tumor with necrosis (P(ADJ)<0.05). Investigation stratifying by stage found that APLP1 and PLPP2 overexpression were significantly associated with poorer OS in the early stage (Quartile 1 vs. Quartile 4, HR = 3.87, 95% CI:1.25-11.97, P = 0.02 and HR = 4.77, 95% CI:1.37-16.57, P = 0.04 respectively). These genes are potential biomarkers of ccRCC aggressiveness and prognosis that direct clinical and surgical management. Impact Journals LLC 2018-05 /pmc/articles/PMC6305109/ /pubmed/30603059 http://dx.doi.org/10.18632/genesandcancer.183 Text en Copyright: © 2018 Batai et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Batai, Ken Imler, Elliot Pangilinan, Jayce Bell, Robert Lwin, Aye Price, Elinora Milinic, Tijana Arora, Amit Ellis, Nathan A. Bracamonte, Erika Seligmann, Bruce Lee, Benjamin R. Whole-transcriptome sequencing identified gene expression signatures associated with aggressive clear cell renal cell carcinoma |
title | Whole-transcriptome sequencing identified gene expression signatures associated with aggressive clear cell renal cell carcinoma |
title_full | Whole-transcriptome sequencing identified gene expression signatures associated with aggressive clear cell renal cell carcinoma |
title_fullStr | Whole-transcriptome sequencing identified gene expression signatures associated with aggressive clear cell renal cell carcinoma |
title_full_unstemmed | Whole-transcriptome sequencing identified gene expression signatures associated with aggressive clear cell renal cell carcinoma |
title_short | Whole-transcriptome sequencing identified gene expression signatures associated with aggressive clear cell renal cell carcinoma |
title_sort | whole-transcriptome sequencing identified gene expression signatures associated with aggressive clear cell renal cell carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305109/ https://www.ncbi.nlm.nih.gov/pubmed/30603059 http://dx.doi.org/10.18632/genesandcancer.183 |
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