Ho Lye Lin, Kench James G, Handelsman David J, Scheffer George L, Stricker Phillip D, Grygiel John G, Sutherland Robert L, Henshall Susan M, Allen John D, Horvath Lisa G
Centenary Institute of Cancer Medicine and Cell Biology, Newtown, NSW 2042, Australia.
Prostate. 2008 Sep 15;68(13):1421-9. doi: 10.1002/pros.20809.
MRP4/ABCC4 is an ATP-binding cassette transporter expressed in normal prostate. This study aimed to define the pattern of MRP4/ABCC4 expression in normal and malignant prostate tissue and the relationship of MRP4/ABCC4 expression and function in response to androgen signaling.
Eighty-four radical prostatectomy specimens from patients with localized prostate cancer (PC) (22 neoadjuvant androgen ablation, AA, 62 no AA), 42 non-cancer and 16 advanced PCs were assessed for MRP4/ABCC4 mRNA/protein expression. The effect of DHT and bicalutamide on LNCaP cells was assessed by immunoblotting. HEK293 cells (+/-MRP4/ABCC4) were assessed for the ability to efflux androgens and anti-androgens.
MRP4/ABCC4 mRNA/protein levels were higher in localized PC compared to non-cancer (P = 0.006). MRP4/ABCC4 levels were significantly decreased in PCs treated with AA compared to cancers exposed to normal testosterone levels (P < 0.0001). MRP4/ABCC4 expression in normal human tissues was limited to the prostate and the renal tubules. MRP4/ABCC4 protein levels increased in LNCaP cells after DHT which was partially blocked by bicalutamide. However, DHT did not alter the activation of the MRP4/ABCC4 promotor in luciferase reporter assays and testosterone, DHT, flutamide and hydroxy-flutamide were not substrates for MRP4/ABCC4.
Elevated MRP4/ABCC4 expression is found in malignant compared to benign prostate tissue while lower MRP4/ABCC4 expression is seen after AA. Furthermore, MRP4/ABCC4 is upregulated by androgen and downregulated by anti-androgen treatment in vitro potentially through an indirect mode of action. These data strongly suggest that MRP4/ABCC4 is an androgen-regulated gene important in the progression to PC and may be a potential drug target.
多药耐药相关蛋白4(MRP4/ABCC4)是一种在正常前列腺组织中表达的ATP结合盒转运蛋白。本研究旨在明确MRP4/ABCC4在正常及恶性前列腺组织中的表达模式,以及MRP4/ABCC4表达与功能在雄激素信号应答中的关系。
对84例局限性前列腺癌(PC)患者的根治性前列腺切除术标本(22例新辅助雄激素去势,AA,62例未行AA)、42例非癌组织标本及16例晚期PC标本进行MRP4/ABCC4 mRNA/蛋白表达评估。通过免疫印迹法评估双氢睾酮(DHT)和比卡鲁胺对LNCaP细胞的作用。对人胚肾293细胞(±MRP4/ABCC4)进行雄激素和抗雄激素外排能力评估。
与非癌组织相比,局限性PC中MRP4/ABCC4 mRNA/蛋白水平更高(P = 0.006)。与暴露于正常睾酮水平的癌症相比,接受AA治疗的PC中MRP4/ABCC4水平显著降低(P < 0.0001)。MRP4/ABCC4在正常人体组织中的表达仅限于前列腺和肾小管。DHT处理后LNCaP细胞中MRP4/ABCC4蛋白水平升高,比卡鲁胺可部分阻断这一升高。然而,在荧光素酶报告基因检测中,DHT并未改变MRP4/ABCC4启动子的激活,且睾酮、DHT、氟他胺和羟基氟他胺不是MRP4/ABCC4的底物。
与良性前列腺组织相比,恶性前列腺组织中MRP4/ABCC4表达升高,而AA后MRP4/ABCC4表达降低。此外,在体外,MRP4/ABCC4可能通过间接作用模式被雄激素上调,被抗雄激素治疗下调。这些数据强烈表明,MRP4/ABCC4是一种在PC进展中起重要作用的雄激素调节基因,可能是一个潜在的药物靶点。