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Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer
The prostate gland mainly contains basal and luminal cells constructed as a pseudostratified epithelium. Annotation of prostate epithelial transcriptomes provides a foundation for discoveries that can impact disease understanding and treatment. Here we describe a genome-wide transcriptome analysis o...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773505/ https://www.ncbi.nlm.nih.gov/pubmed/26924072 http://dx.doi.org/10.1038/ncomms10798 |
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author | Zhang, Dingxiao Park, Daechan Zhong, Yi Lu, Yue Rycaj, Kiera Gong, Shuai Chen, Xin Liu, Xin Chao, Hsueh-Ping Whitney, Pamela Calhoun-Davis, Tammy Takata, Yoko Shen, Jianjun Iyer, Vishwanath R. Tang, Dean G. |
author_facet | Zhang, Dingxiao Park, Daechan Zhong, Yi Lu, Yue Rycaj, Kiera Gong, Shuai Chen, Xin Liu, Xin Chao, Hsueh-Ping Whitney, Pamela Calhoun-Davis, Tammy Takata, Yoko Shen, Jianjun Iyer, Vishwanath R. Tang, Dean G. |
author_sort | Zhang, Dingxiao |
collection | PubMed |
description | The prostate gland mainly contains basal and luminal cells constructed as a pseudostratified epithelium. Annotation of prostate epithelial transcriptomes provides a foundation for discoveries that can impact disease understanding and treatment. Here we describe a genome-wide transcriptome analysis of human benign prostatic basal and luminal epithelial populations using deep RNA sequencing. Through molecular and biological characterizations, we show that the differential gene-expression profiles account for their distinct functional properties. Strikingly, basal cells preferentially express gene categories associated with stem cells, neurogenesis and ribosomal RNA (rRNA) biogenesis. Consistent with this profile, basal cells functionally exhibit intrinsic stem-like and neurogenic properties with enhanced rRNA transcription activity. Of clinical relevance, the basal cell gene-expression profile is enriched in advanced, anaplastic, castration-resistant and metastatic prostate cancers. Therefore, we link the cell-type-specific gene signatures to aggressive subtypes of prostate cancer and identify gene signatures associated with adverse clinical features. |
format | Online Article Text |
id | pubmed-4773505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47735052016-03-04 Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer Zhang, Dingxiao Park, Daechan Zhong, Yi Lu, Yue Rycaj, Kiera Gong, Shuai Chen, Xin Liu, Xin Chao, Hsueh-Ping Whitney, Pamela Calhoun-Davis, Tammy Takata, Yoko Shen, Jianjun Iyer, Vishwanath R. Tang, Dean G. Nat Commun Article The prostate gland mainly contains basal and luminal cells constructed as a pseudostratified epithelium. Annotation of prostate epithelial transcriptomes provides a foundation for discoveries that can impact disease understanding and treatment. Here we describe a genome-wide transcriptome analysis of human benign prostatic basal and luminal epithelial populations using deep RNA sequencing. Through molecular and biological characterizations, we show that the differential gene-expression profiles account for their distinct functional properties. Strikingly, basal cells preferentially express gene categories associated with stem cells, neurogenesis and ribosomal RNA (rRNA) biogenesis. Consistent with this profile, basal cells functionally exhibit intrinsic stem-like and neurogenic properties with enhanced rRNA transcription activity. Of clinical relevance, the basal cell gene-expression profile is enriched in advanced, anaplastic, castration-resistant and metastatic prostate cancers. Therefore, we link the cell-type-specific gene signatures to aggressive subtypes of prostate cancer and identify gene signatures associated with adverse clinical features. Nature Publishing Group 2016-02-29 /pmc/articles/PMC4773505/ /pubmed/26924072 http://dx.doi.org/10.1038/ncomms10798 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhang, Dingxiao Park, Daechan Zhong, Yi Lu, Yue Rycaj, Kiera Gong, Shuai Chen, Xin Liu, Xin Chao, Hsueh-Ping Whitney, Pamela Calhoun-Davis, Tammy Takata, Yoko Shen, Jianjun Iyer, Vishwanath R. Tang, Dean G. Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
title | Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
title_full | Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
title_fullStr | Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
title_full_unstemmed | Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
title_short | Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
title_sort | stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773505/ https://www.ncbi.nlm.nih.gov/pubmed/26924072 http://dx.doi.org/10.1038/ncomms10798 |
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