Expression, regulation and function of the ISGylation system in prostate cancer

被引:51
作者
Kiessling, A. [1 ]
Hogrefe, C. [1 ]
Erb, S. [1 ]
Bobach, C. [2 ]
Fuessel, S. [3 ]
Wessjohann, L. [2 ]
Seliger, B. [1 ]
机构
[1] Univ Halle Wittenberg, Inst Med Immunol, Fac Med, D-06112 Halle, Germany
[2] Leibniz Inst Plant Biochem, Dept Bioorgan Chem, Halle, Germany
[3] Tech Univ Dresden, Dept Urol, Med Fac Carl Gustav Carus, Dresden, Germany
关键词
ISG15; prostate cancer; androgen receptor; androgen-regulated genes; UBIQUITIN-LIKE PROTEIN; ANDROGEN RECEPTOR EXPRESSION; RESPONSIVE FINGER PROTEIN; RAT VENTRAL PROSTATE; HUMAN BREAST-CANCER; ISG15; E3; LIGASE; NEGATIVE REGULATION; EPITHELIAL-CELLS; GENE-EXPRESSION; LUNG-CANCER;
D O I
10.1038/onc.2009.115
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 androgen receptor (AR) plays a crucial role in the modulation of prostate cell proliferation and is involved in the development and progression of prostate cancer (PCa). An understanding of the complex regulation of AR provides novel treatment options for PCa. Here, we show (i) that the ubiquitin-like modifier, interferon-stimulated gene 15 (ISG15), and most enzymes involved in ISG15 conjugation were upregulated in tumor samples versus in non-malignant tissues of PCa patients and (ii) that the expression of these components significantly differed between tumors in patients treated with and without androgen ablation. Using PCa cell lines as in vitro models, the specific androgen-mediated, AR-dependent regulation of the ISGylation components was confirmed. In addition, the ISGylation system controls AR mRNA and protein expressions, as overexpression of Ube1L as a limiting ISGylation factor in the AR(+) androgen-sensitive PCa cell line, LNCaP, results in significant AR upregulation, accompanied by an increased proliferation even under androgen deprivation. Accordingly, Ube1L knockdown decreased the AR expression. Thus, this study describes for the. first time the modulation of AR expression by ISGylation components, which affects the proliferation of PCa cells, thereby providing evidence for a novel function of the ISGylation system in malignant transformation. Oncogene (2009) 28, 2606-2620; doi: 10.1038/onc.2009.115; published online 11 May 2009
引用
收藏
页码:2606 / 2620
页数:15
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