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Long non-coding RNA profiling links subgroup classification of endometrioid endometrial carcinomas with trithorax and polycomb complex aberrations

BACKGROUND: Integrative analysis of endometrioid endometrial carcinoma (EEC) using multiple platforms has distinguished four molecular subgroups. However, the landscape of expressed long non-coding RNAs (lncRNA) and their role in charting EEC subgroups and determining clinical aggressiveness remain...

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Autores principales: Jiang, Yunyun, Malouf, Gabriel G., Zhang, Jianping, Zheng, Xiaofeng, Chen, Yunxin, Thompson, Erika J., Weinstein, John N., Yuan, Ying, Spano, Jean-Philippe, Broaddus, Russell, Tannir, Nizar M., Khayat, David, Lu, Karen H., Su, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741866/
https://www.ncbi.nlm.nih.gov/pubmed/26431491
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author Jiang, Yunyun
Malouf, Gabriel G.
Zhang, Jianping
Zheng, Xiaofeng
Chen, Yunxin
Thompson, Erika J.
Weinstein, John N.
Yuan, Ying
Spano, Jean-Philippe
Broaddus, Russell
Tannir, Nizar M.
Khayat, David
Lu, Karen H.
Su, Xiaoping
author_facet Jiang, Yunyun
Malouf, Gabriel G.
Zhang, Jianping
Zheng, Xiaofeng
Chen, Yunxin
Thompson, Erika J.
Weinstein, John N.
Yuan, Ying
Spano, Jean-Philippe
Broaddus, Russell
Tannir, Nizar M.
Khayat, David
Lu, Karen H.
Su, Xiaoping
author_sort Jiang, Yunyun
collection PubMed
description BACKGROUND: Integrative analysis of endometrioid endometrial carcinoma (EEC) using multiple platforms has distinguished four molecular subgroups. However, the landscape of expressed long non-coding RNAs (lncRNA) and their role in charting EEC subgroups and determining clinical aggressiveness remain largely unknown. MATERIALS AND METHODS: We performed integrative analysis of lncRNAs in EEC using The Cancer Genome Atlas (TCGA) molecular RNAseq profiles of 191 primary tumors for which genomic data were also available. We established lncRNA subgroup classification, correlated it with chromatin modifying gene expression, and described correlations between our lncRNA classification and clinico-genomic tumor features. RESULTS: Using stringent criteria, we identified 1,931 expressed lncRNAs and predicted potential drivers through integrative analysis. Unsupervised clustering of lncRNA expression revealed three robust categories: basal-like, luminal-like and CTNNB1-enriched subgroups. Basal-like subgroup was enriched for aggressive tumors with higher pathological grade (p < 0.0001), TNM stage (p = 0.01), and somatic mutations in trithorax-group genes (MLL, MLL2 and MLL3); and it overexpressed polycomb genes EZH2 and CBX2. In contrast to the luminal-like subgroup, progesterone (PGR) and estrogen receptor (ESR1) genes were highly down-regulated in the EEC basal-like subgroup. Consistent with its enrichment for CTNNB1 mutations (69%), lncRNA profile of the CTNNB1-enriched EEC subgroup was highly similar to that of the CTNNB1-enriched liver cancer subgroup. CONCLUSIONS: Our results reveal the utility of systematic characterization of clinically annotated EEC in three clinically relevant subgroups. They also highlight the convergence of aberrations in polycomb- and trithorax-group genes in aggressive basal EEC subtypes, providing a rationale for further investigation of epigenetic therapy in this setting.
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spelling pubmed-47418662016-03-23 Long non-coding RNA profiling links subgroup classification of endometrioid endometrial carcinomas with trithorax and polycomb complex aberrations Jiang, Yunyun Malouf, Gabriel G. Zhang, Jianping Zheng, Xiaofeng Chen, Yunxin Thompson, Erika J. Weinstein, John N. Yuan, Ying Spano, Jean-Philippe Broaddus, Russell Tannir, Nizar M. Khayat, David Lu, Karen H. Su, Xiaoping Oncotarget Research Paper BACKGROUND: Integrative analysis of endometrioid endometrial carcinoma (EEC) using multiple platforms has distinguished four molecular subgroups. However, the landscape of expressed long non-coding RNAs (lncRNA) and their role in charting EEC subgroups and determining clinical aggressiveness remain largely unknown. MATERIALS AND METHODS: We performed integrative analysis of lncRNAs in EEC using The Cancer Genome Atlas (TCGA) molecular RNAseq profiles of 191 primary tumors for which genomic data were also available. We established lncRNA subgroup classification, correlated it with chromatin modifying gene expression, and described correlations between our lncRNA classification and clinico-genomic tumor features. RESULTS: Using stringent criteria, we identified 1,931 expressed lncRNAs and predicted potential drivers through integrative analysis. Unsupervised clustering of lncRNA expression revealed three robust categories: basal-like, luminal-like and CTNNB1-enriched subgroups. Basal-like subgroup was enriched for aggressive tumors with higher pathological grade (p < 0.0001), TNM stage (p = 0.01), and somatic mutations in trithorax-group genes (MLL, MLL2 and MLL3); and it overexpressed polycomb genes EZH2 and CBX2. In contrast to the luminal-like subgroup, progesterone (PGR) and estrogen receptor (ESR1) genes were highly down-regulated in the EEC basal-like subgroup. Consistent with its enrichment for CTNNB1 mutations (69%), lncRNA profile of the CTNNB1-enriched EEC subgroup was highly similar to that of the CTNNB1-enriched liver cancer subgroup. CONCLUSIONS: Our results reveal the utility of systematic characterization of clinically annotated EEC in three clinically relevant subgroups. They also highlight the convergence of aberrations in polycomb- and trithorax-group genes in aggressive basal EEC subtypes, providing a rationale for further investigation of epigenetic therapy in this setting. Impact Journals LLC 2015-09-26 /pmc/articles/PMC4741866/ /pubmed/26431491 Text en Copyright: © 2015 Jiang 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 Paper
Jiang, Yunyun
Malouf, Gabriel G.
Zhang, Jianping
Zheng, Xiaofeng
Chen, Yunxin
Thompson, Erika J.
Weinstein, John N.
Yuan, Ying
Spano, Jean-Philippe
Broaddus, Russell
Tannir, Nizar M.
Khayat, David
Lu, Karen H.
Su, Xiaoping
Long non-coding RNA profiling links subgroup classification of endometrioid endometrial carcinomas with trithorax and polycomb complex aberrations
title Long non-coding RNA profiling links subgroup classification of endometrioid endometrial carcinomas with trithorax and polycomb complex aberrations
title_full Long non-coding RNA profiling links subgroup classification of endometrioid endometrial carcinomas with trithorax and polycomb complex aberrations
title_fullStr Long non-coding RNA profiling links subgroup classification of endometrioid endometrial carcinomas with trithorax and polycomb complex aberrations
title_full_unstemmed Long non-coding RNA profiling links subgroup classification of endometrioid endometrial carcinomas with trithorax and polycomb complex aberrations
title_short Long non-coding RNA profiling links subgroup classification of endometrioid endometrial carcinomas with trithorax and polycomb complex aberrations
title_sort long non-coding rna profiling links subgroup classification of endometrioid endometrial carcinomas with trithorax and polycomb complex aberrations
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741866/
https://www.ncbi.nlm.nih.gov/pubmed/26431491
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