| Literature DB >> 29944905 |
Yi-Ting Chang1, Tzu-Ping Lin2, Jui-Ting Tang1, Mel Campbell3, Yun-Li Luo1, Shih-Yen Lu4, Chia-Pei Yang1, Ting-Yu Cheng1, Ching-Hsin Chang5, Tze-Tze Liu6, Chi-Hung Lin7, Hsing-Jein Kung8, Chin-Chen Pan9, Pei-Ching Chang10.
Abstract
Long non-coding RNAs (lncRNAs) are emerging as novel diagnostic markers of prostate cancer (PCa) and new determinants of castration-resistant PCa (CRPC), an aggressive and metastatic form of PCa. In addition to androgen receptor (AR) signaling, neuroendocrine differentiation (NED) is associated with CRPC. Recent reports demonstrate that the downregulation of repressor element-1 silencing transcription factor (REST) protein is a key step in NED of PCa cells. Here, we report HOTAIR as a novel REST-repressed lncRNA that is upregulated in NED PCa cells and in CRPC. HOTAIR overexpression is sufficient to induce, whereas knockdown of HOTAIR suppressed NED of PCa cells. Gene ontology (GO) analysis of differentially expressed genes under HOTAIR overexpression and in CRPC versus benign prostatic hyperplasia (BPH) suggests that HOTAIR may participate in PCa progression. Taken together, our results provide the first evidence of lncRNA HOTAIR as a driver for NED of PCa cells.Entities:
Keywords: Castration-resistant prostate cancer; HOTAIR; Long non-coding RNAs; Neuroendocrine differentiation; REST
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Year: 2018 PMID: 29944905 DOI: 10.1016/j.canlet.2018.06.029
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679