作者
Junjie Tony Hua, Musaddeque Ahmed, Haiyang Guo, Yuzhe Zhang, Sujun Chen, Fraser Soares, Jennifer Lu, Stanley Zhou, Miranda Wang, Hui Li, Nicholas B Larson, Shannon K McDonnell, Parasvi S Patel, Yi Liang, Cindy Q Yao, Theodorus van der Kwast, Mathieu Lupien, Felix Y Feng, Amina Zoubeidi, Ming-Sound Tsao, Stephen N Thibodeau, Paul C Boutros, Housheng Hansen He
发表日期
2018/7/26
期刊
Cell
卷号
174
期号
3
页码范围
564-575. e18
出版商
Elsevier
简介
The prostate cancer (PCa) risk-associated SNP rs11672691 is positively associated with aggressive disease at diagnosis. We showed that rs11672691 maps to the promoter of a short isoform of long noncoding RNA PCAT19 (PCAT19-short), which is in the third intron of the long isoform (PCAT19-long). The risk variant is associated with decreased and increased levels of PCAT19-short and PCAT19-long, respectively. Mechanistically, the risk SNP region is bifunctional with both promoter and enhancer activity. The risk variants of rs11672691 and its LD SNP rs887391 decrease binding of transcription factors NKX3.1 and YY1 to the promoter of PCAT19-short, resulting in weaker promoter but stronger enhancer activity that subsequently activates PCAT19-long. PCAT19-long interacts with HNRNPAB to activate a subset of cell-cycle genes associated with PCa progression, thereby promoting PCa tumor growth and …
引用总数
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