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Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer
Clear cell renal cell carcinomas (ccRCC) show a broad range of clinical behavior, and prognostic biomarkers are needed to stratify patients for appropriate management. We sought to determine whether long intergenic non-coding RNAs (lincRNAs) might predict patient survival. Candidate prognostic lincR...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386637/ https://www.ncbi.nlm.nih.gov/pubmed/28423633 http://dx.doi.org/10.18632/oncotarget.15703 |
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author | Gong, Xue Siprashvili, Zurab Eminaga, Okyaz Shen, Zhewei Sato, Yusuke Kume, Haruki Homma, Yukio Ogawa, Seishi Khavari, Paul A. Pollack, Jonathan R. Brooks, James D. |
author_facet | Gong, Xue Siprashvili, Zurab Eminaga, Okyaz Shen, Zhewei Sato, Yusuke Kume, Haruki Homma, Yukio Ogawa, Seishi Khavari, Paul A. Pollack, Jonathan R. Brooks, James D. |
author_sort | Gong, Xue |
collection | PubMed |
description | Clear cell renal cell carcinomas (ccRCC) show a broad range of clinical behavior, and prognostic biomarkers are needed to stratify patients for appropriate management. We sought to determine whether long intergenic non-coding RNAs (lincRNAs) might predict patient survival. Candidate prognostic lincRNAs were identified by mining The Cancer Genome Atlas (TCGA) transcriptome (RNA-seq) data on 466 ccRCC cases (randomized into discovery and validation sets) annotated for ~21,000 lncRNAs. A previously uncharacterized lincRNA, SLINKY (Survival-predictive LINcRNA in KidneY cancer), was the top-ranked prognostic lincRNA, and validated in an independent University of Tokyo cohort (P=0.004). In multivariable analysis, SLINKY expression predicted overall survival independent of tumor stage and grade [TCGA HR=3.5 (CI, 2.2-5.7), P < 0.001; Tokyo HR=8.4 (CI, 1.8-40.2), P = 0.007], and by decision tree, ROC and decision curve analysis, added independent prognostic value. In ccRCC cell lines, SLINKY knockdown reduced cancer cell proliferation (with cell-cycle G(1) arrest) and induced transcriptome changes enriched for cell proliferation and survival processes. Notably, the genes affected by SLINKY knockdown in cell lines were themselves prognostic and correlated with SLINKY expression in the ccRCC patient samples. From a screen for binding partners, we identified direct binding of SLINKY to Heterogeneous Nuclear Ribonucleoprotein K (HNRNPK), whose knockdown recapitulated SLINKY knockdown phenotypes. Thus, SLINKY is a robust prognostic biomarker in ccRCC, where it functions possibly together with HNRNPK in cancer cell proliferation. |
format | Online Article Text |
id | pubmed-5386637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53866372017-04-26 Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer Gong, Xue Siprashvili, Zurab Eminaga, Okyaz Shen, Zhewei Sato, Yusuke Kume, Haruki Homma, Yukio Ogawa, Seishi Khavari, Paul A. Pollack, Jonathan R. Brooks, James D. Oncotarget Priority Research Paper Clear cell renal cell carcinomas (ccRCC) show a broad range of clinical behavior, and prognostic biomarkers are needed to stratify patients for appropriate management. We sought to determine whether long intergenic non-coding RNAs (lincRNAs) might predict patient survival. Candidate prognostic lincRNAs were identified by mining The Cancer Genome Atlas (TCGA) transcriptome (RNA-seq) data on 466 ccRCC cases (randomized into discovery and validation sets) annotated for ~21,000 lncRNAs. A previously uncharacterized lincRNA, SLINKY (Survival-predictive LINcRNA in KidneY cancer), was the top-ranked prognostic lincRNA, and validated in an independent University of Tokyo cohort (P=0.004). In multivariable analysis, SLINKY expression predicted overall survival independent of tumor stage and grade [TCGA HR=3.5 (CI, 2.2-5.7), P < 0.001; Tokyo HR=8.4 (CI, 1.8-40.2), P = 0.007], and by decision tree, ROC and decision curve analysis, added independent prognostic value. In ccRCC cell lines, SLINKY knockdown reduced cancer cell proliferation (with cell-cycle G(1) arrest) and induced transcriptome changes enriched for cell proliferation and survival processes. Notably, the genes affected by SLINKY knockdown in cell lines were themselves prognostic and correlated with SLINKY expression in the ccRCC patient samples. From a screen for binding partners, we identified direct binding of SLINKY to Heterogeneous Nuclear Ribonucleoprotein K (HNRNPK), whose knockdown recapitulated SLINKY knockdown phenotypes. Thus, SLINKY is a robust prognostic biomarker in ccRCC, where it functions possibly together with HNRNPK in cancer cell proliferation. Impact Journals LLC 2017-02-24 /pmc/articles/PMC5386637/ /pubmed/28423633 http://dx.doi.org/10.18632/oncotarget.15703 Text en Copyright: © 2017 Gong et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Priority Research Paper Gong, Xue Siprashvili, Zurab Eminaga, Okyaz Shen, Zhewei Sato, Yusuke Kume, Haruki Homma, Yukio Ogawa, Seishi Khavari, Paul A. Pollack, Jonathan R. Brooks, James D. Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer |
title | Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer |
title_full | Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer |
title_fullStr | Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer |
title_full_unstemmed | Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer |
title_short | Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer |
title_sort | novel lincrna slinky is a prognostic biomarker in kidney cancer |
topic | Priority Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386637/ https://www.ncbi.nlm.nih.gov/pubmed/28423633 http://dx.doi.org/10.18632/oncotarget.15703 |
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