Identification and Characterization of PCAHIT, a Novel Long Non-Coding RNA Associated with Poor Outcomes in Prostate Cancer
Hui LiiD, Noah Spector YoungeriD, Bhavna Malik, Hyun Jin Shin, Chao ZhangiD, Yashar S. Niknafs, Shuang ZhaoiD, Kari Wilder-RomansiD, Sethuramasundaram PitchiayaiD, Jasmine Anderson, Sumin HaniD, Travis J. Barnard, Paul LloydiD, Meng ZhangiD, Lisa N. ChesneriD, Marsha Calvert, Emily A. EgusaiD, Jonathan ChouiD, Rajdeep DasiD, Vishal Kothari, Tanu Shenoy, Morgan E. DiolaitiiD, Rohit MalikiD, John R. PrensneriD, Alma L. BurlingameiD, , Haolong LiiD
Abstract
Background: Despite extensive investigation, the factors promoting aggressive prostate cancer are poorly understood. In particular, despite a few prominent examples, the role of long non-coding RNAs (lncRNAs) is largely unknown. Methods: We performed a comprehensive analysis of whole-genome transcriptome data to identify differential expression across 1,567 patients with prostate cancer, then correlated differential expression with risk of metastatic recurrence. We characterized the lncRNA most associated with metastasis in vitro and in vivo to investigate the mechanism by which it promotes aggressive prostate cancer. Results: We have identified a novel lncRNA, Prostate Cancer Associated hnRNPK Interacting Transcript (PCAHIT), which is strongly associated with metastasis and poor overall survival in men with prostate cancer. We find that overexpression/knockdown of PCAHIT in pre-clinical models of prostate cancer modulates proliferation rates and markers of an aggressive phenotype through regulation of steroid biosynthesis and expression of the MHC class I complex, driving increased growth in androgen-depleted conditions and decreased susceptibility to T cell-mediated cytotoxicity. We further find that the heterogeneous nuclear ribonucleoprotein hnRNPK directly binds PCAHIT and is indispensable for its activity. Conclusions: Overall, our findings indicate that PCAHIT is a driver of aggressive prostate cancer phenotypes and poor clinical outcomes through suppression of the immune response and increased androgen-independent cancer growth. PCAHIT is a potential biomarker of aggressive disease.
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