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The lncRNAs PCGEM1 and PRNCR1 are not implicated in castration resistant prostate cancer
Long noncoding RNAs (lncRNAs) are increasingly implicated in cancer biology, contributing to essential cancer cell functions such as proliferation, invasion, and metastasis. In prostate cancer, several lncRNAs have been nominated as critical actors in disease pathogenesis. Among these, expression of...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039221/ https://www.ncbi.nlm.nih.gov/pubmed/24727738 |
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author | Prensner, John R. Sahu, Anirban Iyer, Matthew K. Malik, Rohit Chandler, Benjamin Asangani, Irfan A. Poliakov, Anton Vergara, Ismael A. Alshalalfa, Mohammed Jenkins, Robert B. Davicioni, Elai Feng, Felix Y. Chinnaiyan, Arul M. |
author_facet | Prensner, John R. Sahu, Anirban Iyer, Matthew K. Malik, Rohit Chandler, Benjamin Asangani, Irfan A. Poliakov, Anton Vergara, Ismael A. Alshalalfa, Mohammed Jenkins, Robert B. Davicioni, Elai Feng, Felix Y. Chinnaiyan, Arul M. |
author_sort | Prensner, John R. |
collection | PubMed |
description | Long noncoding RNAs (lncRNAs) are increasingly implicated in cancer biology, contributing to essential cancer cell functions such as proliferation, invasion, and metastasis. In prostate cancer, several lncRNAs have been nominated as critical actors in disease pathogenesis. Among these, expression of PCGEM1 and PRNCR1 has been identified as a possible component in disease progression through the coordination of androgen receptor (AR) signaling (Yang et al., Nature 2013, see ref. [1]). However, concerns regarding the robustness of these findings have been suggested. Here, we sought to evaluate whether PCGEM1 and PRNCR1 are associated with prostate cancer. Through a comprehensive analysis of RNA-sequencing data (RNA-seq), we find evidence that PCGEM1 but not PRNCR1 is associated with prostate cancer. We employ a large cohort of >230 high-risk prostate cancer patients with long-term outcomes data to show that, in contrast to prior reports, neither gene is associated with poor patient outcomes. We further observe no evidence that PCGEM1 nor PRNCR1 interact with AR, and neither gene is a component of AR signaling. Thus, we conclusively demonstrate that PCGEM1 and PRNCR1 are not prognostic lncRNAs in prostate cancer and we refute suggestions that these lncRNAs interact in AR signaling. |
format | Online Article Text |
id | pubmed-4039221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-40392212014-06-04 The lncRNAs PCGEM1 and PRNCR1 are not implicated in castration resistant prostate cancer Prensner, John R. Sahu, Anirban Iyer, Matthew K. Malik, Rohit Chandler, Benjamin Asangani, Irfan A. Poliakov, Anton Vergara, Ismael A. Alshalalfa, Mohammed Jenkins, Robert B. Davicioni, Elai Feng, Felix Y. Chinnaiyan, Arul M. Oncotarget Research Perspective Long noncoding RNAs (lncRNAs) are increasingly implicated in cancer biology, contributing to essential cancer cell functions such as proliferation, invasion, and metastasis. In prostate cancer, several lncRNAs have been nominated as critical actors in disease pathogenesis. Among these, expression of PCGEM1 and PRNCR1 has been identified as a possible component in disease progression through the coordination of androgen receptor (AR) signaling (Yang et al., Nature 2013, see ref. [1]). However, concerns regarding the robustness of these findings have been suggested. Here, we sought to evaluate whether PCGEM1 and PRNCR1 are associated with prostate cancer. Through a comprehensive analysis of RNA-sequencing data (RNA-seq), we find evidence that PCGEM1 but not PRNCR1 is associated with prostate cancer. We employ a large cohort of >230 high-risk prostate cancer patients with long-term outcomes data to show that, in contrast to prior reports, neither gene is associated with poor patient outcomes. We further observe no evidence that PCGEM1 nor PRNCR1 interact with AR, and neither gene is a component of AR signaling. Thus, we conclusively demonstrate that PCGEM1 and PRNCR1 are not prognostic lncRNAs in prostate cancer and we refute suggestions that these lncRNAs interact in AR signaling. Impact Journals LLC 2014-03-23 /pmc/articles/PMC4039221/ /pubmed/24727738 Text en Copyright: © 2014 Prensner et al. http://creativecommons.org/licenses/by/2.5/ 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 | Research Perspective Prensner, John R. Sahu, Anirban Iyer, Matthew K. Malik, Rohit Chandler, Benjamin Asangani, Irfan A. Poliakov, Anton Vergara, Ismael A. Alshalalfa, Mohammed Jenkins, Robert B. Davicioni, Elai Feng, Felix Y. Chinnaiyan, Arul M. The lncRNAs PCGEM1 and PRNCR1 are not implicated in castration resistant prostate cancer |
title | The lncRNAs PCGEM1 and PRNCR1 are not implicated in castration resistant prostate cancer |
title_full | The lncRNAs PCGEM1 and PRNCR1 are not implicated in castration resistant prostate cancer |
title_fullStr | The lncRNAs PCGEM1 and PRNCR1 are not implicated in castration resistant prostate cancer |
title_full_unstemmed | The lncRNAs PCGEM1 and PRNCR1 are not implicated in castration resistant prostate cancer |
title_short | The lncRNAs PCGEM1 and PRNCR1 are not implicated in castration resistant prostate cancer |
title_sort | lncrnas pcgem1 and prncr1 are not implicated in castration resistant prostate cancer |
topic | Research Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039221/ https://www.ncbi.nlm.nih.gov/pubmed/24727738 |
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