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雄激素对前列腺癌中多药耐药相关蛋白4(MRP4/ABCC4)的调控

Androgen regulation of multidrug resistance-associated protein 4 (MRP4/ABCC4) in prostate cancer.

作者信息

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

机构信息

Centenary Institute of Cancer Medicine and Cell Biology, Newtown, NSW 2042, Australia.

出版信息

Prostate. 2008 Sep 15;68(13):1421-9. doi: 10.1002/pros.20809.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

DISCUSSION

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.

摘要

背景

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。

方法

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。

结果

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。

讨论

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。

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