Post-transcriptional Gene Regulation by MicroRNA-194 Promotes Neuroendocrine Transdifferentiation in Prostate Cancer

被引:40
作者
Fernandes, Rayzel C. [1 ,2 ]
Toubia, John [3 ,4 ]
Townley, Scott [1 ,2 ]
Hanson, Adrienne R. [1 ,2 ]
Dredge, B. Kate [4 ,5 ]
Pillman, Katherine A. [4 ,5 ]
Bert, Andrew G. [4 ,5 ]
Winter, Jean M. [1 ,2 ]
Iggo, Richard [1 ,2 ,6 ]
Das, Rajdeep [1 ,2 ,7 ]
Obinata, Daisuke [8 ,9 ]
Sandhu, Shahneen [10 ,11 ]
Risbridger, Gail P. [9 ,10 ,11 ]
Taylor, Renea A. [10 ,12 ]
Lawrence, Mitchell G. [9 ,10 ]
Butler, Lisa M. [13 ,14 ]
Zoubeidi, Amina [15 ]
Gregory, Philip A. [4 ,5 ,14 ]
Tilley, Wayne D. [1 ,2 ]
Hickey, Theresa E. [1 ,2 ]
Goodall, Gregory J. [4 ,5 ,16 ]
Selth, Luke A. [1 ,2 ,17 ]
机构
[1] Univ Adelaide, Dame Roma Mitchell Canc Res Labs, Adelaide Med Sch, Adelaide, SA 5005, Australia
[2] Univ Adelaide, Freemasons Fdn Ctr Mens Hlth, Adelaide Med Sch, Adelaide, SA 5005, Australia
[3] Ctr Canc Biol, Alliance SA Pathol, ACRF Canc Genom Facil, Frome Rd, Adelaide, SA 5005, Australia
[4] Univ South Australia, Frome Rd, Adelaide, SA 5005, Australia
[5] Ctr Canc Biol, Alliance SA Pathol, Adelaide, SA 5005, Australia
[6] Inst Bergonie Unicanc, INSERM U1218, Bordeaux, France
[7] Northwestern Univ, Transplant Immunol Lab, Comprehens Transplant Ctr, Feinberg Sch Med, Chicago, IL 60611 USA
[8] Nihon Univ, Dept Urol, Sch Med, Tokyo 1738610, Japan
[9] Monash Univ, Dept Anat & Dev Biol, Monash Partners Comprehens Canc Consortium, Monash Biomed Discovery Inst,Prostate Canc Res Gr, Clayton, Vic 3168, Australia
[10] Univ Melbourne, Peter MacCallum Canc Ctr, Canc Res Div, Canc Res Program, Melbourne, Vic 3000, Australia
[11] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic 3000, Australia
[12] Monash Univ, Monash Biomed Discovery Inst, Dept Physiol, Prostate Canc Res Grp,Monash Partners Comprehens, Clayton, Vic 3168, Australia
[13] South Australian Hlth & Med Res Inst, Adelaide, SA 5000, Australia
[14] Univ Adelaide, Fac Hlth & Med Sci, Adelaide, SA 5005, Australia
[15] Univ British Columbia, Vancouver Prostate Ctr, Vancouver, BC V6H 3Z6, Canada
[16] Univ Adelaide, Sch Biol Sci, Adelaide, SA 5005, Australia
[17] Flinders Univ S Australia, Flinders Hlth & Med Res Inst, Bedford Pk, SA 5042, Australia
基金
英国医学研究理事会;
关键词
TRANSCRIPTION FACTORS; MAMMALIAN MICRORNAS; LINEAGE PLASTICITY; RECEPTOR; DIFFERENTIATION; ACTIVATION; REVEALS; BINDING; FOXA1; IDENTIFICATION;
D O I
10.1016/j.celrep.2020.108585
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Potent therapeutic inhibition of the androgen receptor (AR) in prostate adenocarcinoma can lead to the emergence of neuroendocrine prostate cancer (NEPC), a phenomenon associated with enhanced cell plasticity. Here, we show that microRNA-194 (miR-194) is a regulator of epithelial-neuroendocrine transdifferentiation. In clinical prostate cancer samples, miR-194 expression and activity were elevated in NEPC and inversely correlated with AR signaling. miR-194 facilitated the emergence of neuroendocrine features in prostate cancer cells, a process mediated by its ability to directly target a suite of genes involved in cell plasticity. One such target was FOXA1, which encodes a transcription factor with a vital role in maintaining the prostate epithelial lineage. Importantly, a miR-194 inhibitor blocked epithelial-neuroendocrine transdifferentiation and inhibited the growth of cell lines and patient-derived organoids possessing neuroendocrine features. Overall, our study reveals a post-transcriptional mechanism regulating the plasticity of prostate cancer cells and provides a rationale for targeting miR-194 in NEPC.
引用
收藏
页数:23
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