Loss of Wave1 gene defines a subtype of lethal prostate cancer

被引:11
作者
Sowalsky, Adam G. [1 ,5 ]
Sager, Rebecca [2 ]
Schaefer, Rachel J. [1 ]
Bratslavsky, Gennady [3 ]
Pandolfi, Pier Paolo [1 ,4 ,5 ]
Balk, Steven P. [1 ,5 ]
Kotula, Leszek [2 ,3 ]
机构
[1] Harvard Univ, Sch Med, Dept Med, Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[2] SUNY Upstate Med Univ, Dept Biochem & Mol Biol, Syracuse, NY 13210 USA
[3] SUNY Upstate Med Univ, Dept Urol, Syracuse, NY 13210 USA
[4] Harvard Univ, Sch Med, Dept Pathol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Canc Res Inst, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
WAVE; prostate cancer; genomics; androgen receptor; castration resistance; TUMOR-SUPPRESSOR; RUFFLE FORMATION; PI-3; KINASE; N-WASP; PTEN; ANDROGEN; COMPLEX; EXPRESSION; ABI1; BINDING;
D O I
10.18632/oncotarget.3564
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genetic alterations involving TMPRSS2-ERG alterations and deletion of key tumor suppressor genes are associated with development and progression of prostate cancer (PCa). However, less defined are early events that may contribute to the development of high-risk metastatic prostate cancer. Bioinformatic analysis of existing tumor genomic data from PCa patients revealed that WAVE complex gene alterations are associated with a greater likelihood of prostate cancer recurrence. Further analysis of primary vs. castration resistant prostate cancer indicate that disruption of WAVE complex gene expression, and particularly WAVE1 gene (WASF1) loss, is also associated with castration resistance, where WASF1 is frequently co-deleted with PTEN and resists androgen deprivation therapy (ADT). Hence, we propose that WASF1 status defines a subtype of ADT-resistant patients. Better understanding of the effects of WAVE pathway disruption will lead to development of better diagnostic and treatment modalities.
引用
收藏
页码:12383 / 12391
页数:9
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