A role for GATA-2 in transition to an aggressive phenotype in prostate cancer through modulation of key androgen-regulated genes

被引:70
作者
Boehm, M. [1 ]
Locke, W. J. [1 ]
Sutherland, R. L. [1 ]
Kench, J. G. [1 ,2 ]
Henshall, S. M. [1 ]
机构
[1] Garvan Inst Med Res, Canc Res Program, Sydney, NSW 2010, Australia
[2] Royal Prince Alfred Hosp, Dept Anat Pathol, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
AR; GATA-2; prostate cancer; progression; LIPID MOBILIZING FACTOR; TRANSCRIPTION FACTORS; RECEPTOR; EXPRESSION; CELLS; ADIPOCYTES; EVOLUTION; PATHWAY; MODEL;
D O I
10.1038/onc.2009.243
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
GATA-2, a member of the GATA family of transcription factors, is involved in androgen receptor (AR) signaling, however, little is known regarding its role in prostate cancer. Here, we report that GATA-2 is expressed in a substantial proportion of prostate cancers and that high expression of GATA-2 is associated with biochemical recurrence and distant metastatic progression in a validation set of 203 cancers. In vitro data show that GATA-2 is directly recruited to the promoter region of the AR upon androgen stimulation of LNCaP prostate cancer cells with 5 alpha-dihydroxytestosterone (DHT) for 24 h. Ectopic GATA-2 expression causes the induction of AR transcript levels under androgen-depleted conditions (P<0.05). The expression of the AR target gene, AZGP1, is induced upon androgen stimulation and this effect is repressed by GATA-2. In contrast, GATA-2 significantly increases transcript levels of KLK2, which increases further in a time-dependent manner on DHT treatment and in the presence of GATA-2. These results indicate that upregulation of GATA-2 may contribute to the progression to aggressive prostate cancer through modulation of expression of AR and key androgen-regulated genes, one of which, AZGP1, is associated with the progression to metastatic disease. Oncogene (2009) 28, 3847-3856; doi:10.1038/onc.2009.243; published online 17 August 2009
引用
收藏
页码:3847 / 3856
页数:10
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