Department of Clinical Oncology, Leiden University Medical Centre, Leiden, The Netherlands.
Cancer Biol Ther. 2013 May;14(5):401-10. doi: 10.4161/cbt.23759. Epub 2013 Feb 1.
The N-myc downstream regulated gene 1 (NDRG1) has been identified as a metastasis-suppressor gene in prostate cancer (PCa). Compounds targeting PCa cells deficient in NDRG1 could potentially decrease invasion/metastasis of PCa. A cell based screening strategy was employed to identify small molecules that selectively target NDRG1 deficient PCa cells. DU-145 PCa cells rendered deficient in NDRG1 expression by a lentiviral shRNA-mediated knockdown strategy were used in the primary screen. Compounds filtered from the primary screen were further validated through proliferation and clonogenic survival assays in parental and NDRG1 knockdown PCa cells. Screening of 3360 compounds revealed irinotecan and cetrimonium bromide (CTAB) as compounds that exhibited synthetic lethality against NDRG1 deficient PCa cells. A three-dimensional (3-D) invasion assay was utilized to test the ability of CTAB to inhibit invasion of DU-145 cells. CTAB was found to remarkably decrease invasion of DU-145 cells in collagen matrix. Our results suggest that CTAB and irinotecan could be further explored for their potential clinical benefit in patients with NDRG1 deficient PCa.
N- 神经嵴衍生基因 1(NDRG1)已被鉴定为前列腺癌(PCa)中的转移抑制基因。针对 NDRG1 缺乏的前列腺癌细胞的化合物可能潜在地降低 PCa 的侵袭/转移。采用基于细胞的筛选策略来鉴定选择性靶向 NDRG1 缺乏的前列腺癌细胞的小分子。使用慢病毒 shRNA 介导的敲低策略使 DU-145 PCa 细胞中 NDRG1 表达缺失,用于初级筛选。从初级筛选中筛选出的化合物通过在亲本和 NDRG1 敲低的 PCa 细胞中进行增殖和集落存活测定进一步验证。对 3360 种化合物进行筛选,发现伊立替康和十六烷基三甲基溴化铵(CTAB)是对 NDRG1 缺乏的前列腺癌细胞具有合成致死作用的化合物。利用三维(3-D)侵袭测定来测试 CTAB 抑制 DU-145 细胞侵袭的能力。发现 CTAB 可显著降低 DU-145 细胞在胶原基质中的侵袭。我们的结果表明,CTAB 和伊立替康可进一步探索其在 NDRG1 缺乏的 PCa 患者中的潜在临床益处。