Comprehensive analysis of long non-coding RNAs in human breast cancer clinical subtypes

• Published in: Oncotarget Vol. 5; no. 20; pp. 9864 - 9876
• Main Authors: Su, Xiaoping, Malouf, Gabriel G., Chen, Yunxin, Zhang, Jianping, Yao, Hui, Valero, Vicente, Weinstein, John N., Spano, Jean-Philippe, Meric-Bernstam, Funda, Khayat, David, Esteva, Francisco J.
• Format: Journal Article
• Language: English
• Published: United States Impact Journals LLC 30.10.2014
• Subjects: Breast Neoplasms - classification; Breast Neoplasms - genetics; Breast Neoplasms - metabolism; Cell Transformation, Neoplastic - genetics; Female; Gene Expression; Humans; MCF-7 Cells; Receptor, ErbB-2 - biosynthesis; Research Paper; RNA, Long Noncoding - analysis; RNA, Long Noncoding - biosynthesis; RNA, Long Noncoding - classification; RNA, Long Noncoding - genetics; RNA, Messenger - genetics; RNA, Messenger - metabolism; Survival Rate
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/oncotarget.2454

Accumulating evidence highlights the potential role of long non-coding RNAs (lncRNAs) as biomarkers and therapeutic targets in solid tumors. However, the role of lncRNA expression in human breast cancer biology, prognosis and molecular classification remains unknown. Herein, we established the lncRNA profile of 658 infiltrating ductal carcinomas of the breast from The Cancer Genome Atlas project. We found lncRNA expression to correlate with the gene expression and chromatin landscape of human mammary epithelial cells (non-transformed) and the breast cancer cell line MCF-7. Unsupervised consensus clustering of lncRNA revealed four subgroups that displayed different prognoses. Gene set enrichment analysis for cis- and trans-acting lncRNAs showed enrichment for breast cancer signatures driven by master regulators of breast carcinogenesis. Interestingly, the lncRNA HOTAIR was significantly overexpressed in the HER2-enriched subgroup, while the lncRNA HOTAIRM1 was significantly overexpressed in the basal-like subgroup. Estrogen receptor (ESR1) expression was associated with distinct lncRNA networks in lncRNA clusters III and IV. Importantly, almost two thirds of the lncRNAs were marked by enhancer chromatin modifications (i.e., H3K27ac), suggesting that expressed lncRNA in breast cancer drives carcinogenesis through increased activity of neighboring genes. In summary, our study depicts the first lncRNA subtype classification in breast cancer and provides the framework for future studies to assess the interplay between lncRNAs and the breast cancer epigenome.