Palmitoyl acyltransferase ZDHHC7 inhibits androgen receptor and suppresses prostate cancer

被引:8
|
作者
Lin, Zhuoyuan [1 ,2 ]
Agarwal, Shivani [1 ]
Tan, Song [1 ]
Shi, Hongshun [1 ]
Lu, Xiaodong [1 ]
Tao, Zhipeng [3 ]
Dong, Xuesen [4 ]
Wu, Xu [3 ]
Zhao, Jonathan C. [1 ]
Yu, Jindan [1 ,5 ,6 ]
机构
[1] Northwestern Univ, Dept Med, Div Hematol Oncol, Feinberg Sch Med, Chicago, IL 60611 USA
[2] Guangzhou Med Univ, Dept Urol, Affiliated Hosp 2, Guangzhou, Peoples R China
[3] Harvard Med Sch, Massachusetts Gen Hosp, Cutaneous Biol Res Ctr, Charlestown, MA USA
[4] Univ British Columbia, Vancouver Prostate Ctr, Dept Urol Sci, 2660 Oak St, Vancouver V6H 3Z6, BC, Canada
[5] Emory Univ, Winship Canc Inst, Sch Med, Atlanta, GA 30307 USA
[6] Emory Univ, Dept Urol, Sch Med, Atlanta, GA 30307 USA
关键词
POLYCOMB; CASTRATION; RESISTANCE;
D O I
10.1038/s41388-023-02718-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The hormonal transcription factor androgen receptor (AR) is a master regulator of prostate cancer (PCa). Protein palmitoylation, which attaches a palmitate fatty acid to a substrate protein, is mediated by a class of 23 ZDHHC (Zinc-Finger DHHC motif)-family palmitoyltransferases. Although palmitoylation has been shown to modify many proteins and regulate diverse cellular processes, little is known about ZDHHC genes in cancer. Here we examined ZDHHC family gene expression in human tissue panels and identified ZDHHC7 as a PCa-relevant member. RNA-seq analyses of PCa cells with ZDHHC7 de-regulation revealed global alterations in androgen response and cell cycle pathways. Mechanistically, ZDHHC7 inhibits AR gene transcription and therefore reduces AR protein levels and abolishes AR signaling in PCa cells. Accordingly, ZDHHC7 depletion increased the oncogenic properties of PCa cells, whereas restoring ZDHHC7 is sufficient to suppress PCa cell proliferation and invasion in vitro and mitigate xenograft tumor growth in vivo. Lastly, we demonstrated that ZDHHC7 is downregulated in human PCa compared to benign-adjacent tissues, and its loss is associated with worse clinical outcomes. In summary, our study reveals a global role of ZDHHC7 in inhibiting androgen response and suppressing PCa progression and identifies ZDHHC7 loss as a biomarker for aggressive PCa and a target for therapeutic intervention.
引用
收藏
页码:2126 / 2138
页数:13
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