Ko Y H, Ha Y R, Kim J W, Kang S G, Jang H A, Kang S H, Park H S, Cheon J
Department of Urology, Korea University School of Medicine, Seoul, Republic of Korea.
J Int Med Res. 2011;39(3):729-39. doi: 10.1177/147323001103900304.
This study investigated the mechanism of action of a gonadotropin-releasing hormone (GnRH) agonist, leuprolide, on proliferation of the hormone-refractory prostate cancer cell line DU145, transfected with short hairpin RNA (shRNA), to reduce expression of the GNRHR1 gene (which encodes the GnRH type 1 receptor). DU145 cell proliferation in the presence of leuprolide (10(-9) and 10(-7) M) or control medium was measured before and after GnRHR1 knockdown. Reverse transcription-polymerase chain reaction and Western blot analysis were used to measure the degree of GNRHR1 silencing. DU145 cells treated with leuprolide (10(-9) and 10(-7) M) showed significant growth inhibition compared with control-treated DU145 cells. Transfection with GNRHR1 -shRNA significantly decreased GNRHR1 expression at 48 h. DU145 cells transfected with silencing GNRHR1 -shRNA showed normal growth patterns; however, there was no significant inhibition of proliferation of DU145 cells transfected with GNRHR1 -shRNA compared with cells transfected with control-shRNA in response to leuprolide. These data demonstrated that the antiproliferative effect of leuprolide was mediated by the GnRHR1.
本研究调查了促性腺激素释放激素(GnRH)激动剂亮丙瑞林对转染短发夹RNA(shRNA)以降低GNRHR1基因(编码GnRH 1型受体)表达的激素难治性前列腺癌细胞系DU145增殖的作用机制。在GnRHR1基因敲低前后,测量了亮丙瑞林(10^(-9)和10^(-7) M)或对照培养基存在下DU145细胞的增殖情况。采用逆转录-聚合酶链反应和蛋白质免疫印迹分析来测定GNRHR1沉默的程度。与对照处理的DU145细胞相比,用亮丙瑞林(10^(-9)和10^(-7) M)处理的DU145细胞显示出显著的生长抑制。用GNRHR1 -shRNA转染在48小时时显著降低了GNRHR1的表达。用沉默GNRHR1 -shRNA转染的DU145细胞显示出正常的生长模式;然而,与用对照shRNA转染的细胞相比,用GNRHR1 -shRNA转染的DU145细胞在对亮丙瑞林的反应中增殖没有受到显著抑制。这些数据表明,亮丙瑞林的抗增殖作用是由GnRHR1介导的。