Analysis of the androgen receptor-regulated lncRNA landscape identifies a role for ARLNC1 in prostate cancer progression

被引:188
作者
Zhang, Yajia [1 ,2 ,3 ,4 ]
Pitchiaya, Sethuramasundaram [1 ,2 ]
Cieslik, Marcin [1 ,2 ]
Niknafs, Yashar S. [1 ,5 ]
Tien, Jean C. -Y. [1 ,2 ]
Hosono, Yasuyuki [1 ]
Iyer, Matthew K. [1 ,4 ]
Yazdani, Sahr [1 ]
Subramaniam, Shruthi [1 ]
Shukla, Sudhanshu K. [1 ,21 ]
Jiang, Xia [1 ]
Wang, Lisha [1 ]
Liu, Tzu-Ying [6 ]
Uhl, Michael [7 ,8 ]
Gawronski, Alexander R. [9 ]
Qiao, Yuanyuan [1 ,2 ,10 ]
Xiao, Lanbo [1 ]
Dhanasekaran, Saravana M. [1 ,2 ]
Juckette, Kristin M. [1 ]
Kunju, Lakshmi P. [1 ,2 ,10 ]
Cao, Xuhong [1 ,11 ]
Patel, Utsav [12 ]
Batish, Mona [12 ,13 ]
Shukla, Girish C. [14 ]
Paulsen, Michelle T. [10 ,15 ]
Ljungman, Mats [10 ,15 ]
Jiang, Hui [6 ,10 ]
Mehra, Rohit [2 ,10 ,16 ]
Backofen, Rolf [7 ,8 ]
Sahinalp, Cenk S. [17 ,18 ]
Freier, Susan M. [19 ]
Watt, Andrew T. [19 ]
Guo, Shuling [19 ]
Wei, John T. [16 ]
Feng, Felix Y. [1 ,10 ,15 ,20 ,22 ,23 ,24 ]
Malik, Rohit [1 ,25 ]
Chinnaiyan, Arul M. [1 ,2 ,4 ,5 ,10 ,11 ,16 ]
机构
[1] Univ Michigan, Michigan Ctr Translat Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Mol & Cellular Pathol Program, Ann Arbor, MI 48109 USA
[4] Dept Computat Med & Bioinformat, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Cellular & Mol Biol, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
[7] Univ Freiburg, Dept Comp Sci, Freiburg, Germany
[8] Univ Freiburg, Ctr Biol Signaling Studies BIOSS, Freiburg, Germany
[9] Simon Fraser Univ, Sch Comp Sci, Burnaby, BC, Canada
[10] Univ Michigan, Rogel Canc Ctr, Ann Arbor, MI 48109 USA
[11] Univ Michigan, Howard Hughes Med Inst, Ann Arbor, MI 48109 USA
[12] Rutgers State Univ, New Jersey Med Sch, Newark, NJ USA
[13] Univ Delaware, Dept Med Lab Sci, Newark, DE USA
[14] Cleveland State Univ, Ctr Gene Regulat Hlth & Dis, Dept Biol Geol & Environm Sci, Cleveland, OH 44115 USA
[15] Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[16] Univ Michigan, Dept Urol, Ann Arbor, MI 48109 USA
[17] Indiana Univ, Sch Informat & Comp, Bloomington, IN USA
[18] Vancouver Prostate Ctr, Vancouver, BC, Canada
[19] Ionis Pharmaceut, Carlsbad, CA USA
[20] Univ Michigan, Breast Oncol Program, Ann Arbor, MI 48109 USA
[21] Indian Inst Technol Dharwad, Dept Biosci & Bioengn, Dharwad, Karnataka, India
[22] Univ Calif San Francisco, Dept Radiat Oncol, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA USA
[23] Univ Calif San Francisco, Dept Urol, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA USA
[24] Univ Calif San Francisco, Dept Med, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA USA
[25] Bristol Myers Squibb, Princeton, NJ USA
关键词
LONG NONCODING RNA; GENE-EXPRESSION DATA; MESSENGER-RNA; ANTISENSE OLIGONUCLEOTIDES; DEPRIVATION THERAPY; HUMAN TRANSCRIPTOME; ANTITUMOR-ACTIVITY; INCREASED SURVIVAL; ABIRATERONE; CASTRATION;
D O I
10.1038/s41588-018-0120-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The androgen receptor (AR) plays a critical role in the development of the normal prostate as well as prostate cancer. Using an integrative transcriptomic analysis of prostate cancer cell lines and tissues, we identified ARLNC1 (AR-regulated long noncoding RNA 1) as an important long noncoding RNA that is strongly associated with AR signaling in prostate cancer progression. Not only was ARLNC1 induced by the AR protein, but ARLNC1 stabilized the AR transcript via RNA-RNA interaction. ARLNC1 knockdown suppressed AR expression, global AR signaling and prostate cancer growth in vitro and in vivo. Taken together, these data support a role for ARLNC1 in maintaining a positive feedback loop that potentiates AR signaling during prostate cancer progression and identify ARLNC1 as a novel therapeutic target.
引用
收藏
页码:814 / +
页数:17
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