| Literature DB >> 27096814 |
Francesco Crea1,2, Erik Venalainen1, Xinpei Ci1,3, Hongwei Cheng1,3, Larissa Pikor4, Abhijit Parolia1, Hui Xue1, Nur Ridzwan Nur Saidy1, Dong Lin1,3, Wan Lam4, Colin Collins3, Yuzhuo Wang1,3.
Abstract
Neuroendocrine prostate cancer (NEPC) is the most lethal prostatic neoplasm. NEPC is thought to originate from the transdifferentiation of AR-positive adenocarcinoma cells. We have previously shown that an epigenetic/noncoding interactome (ENI) orchestrates cancer cells' plasticity, thereby allowing the emergence of metastatic, drug-resistant neoplasms. The primary objective of this manuscript is to discuss evidence indicating that some components of the ENI (Polycomb genes, miRNAs) play a key role in NEPC initiation and progression. Long noncoding RNAs represent vast and largely unexplored component of the ENI. Their role in NEPC has not been investigated. We show preliminary evidence indicating that a lncRNA (MIAT) is selectively upregulated in NEPCs and might interact with Polycomb genes. Our results indicate that long noncoding RNAs can be exploited as new biomarkers and therapeutic targets for NEPC.Entities:
Keywords: MIAT; Polycomb; epigenetic/noncoding interactome; long noncoding RNAs; neuroendocrine prostate cancer; transdifferentiation
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Year: 2016 PMID: 27096814 DOI: 10.2217/epi.16.6
Source DB: PubMed Journal: Epigenomics ISSN: 1750-192X Impact factor: 4.778