Institute of Cellular and System Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.
Institute of Biotechnology, National Tsing Hua University, Hsinchu City 30013, Taiwan.
Cells. 2019 Mar 30;8(4):295. doi: 10.3390/cells8040295.
Patients receiving docetaxel developed a drug resistance within a few months. We generated docetaxel-resistant PC/DX25 and DU/DX50 CRPC cells from PC-3 and DU-145 PCa cells, respectively. We investigated the mechanism behind why PC/DX25 and DU/DX50 cells exhibited higher migration and invasion ability. Transwell assays were used to measure the migration and invasion of PCa cell. Fluorescence activated cell sorter (FACS) analysis was used to determine the population of cancer stem cell (CSC)-like cell. Micro-Western Array (MWA) was used to study the changes of the protein profile. FACS analysis revealed that PC/DX25 cells and DU/DX50 cells contain higher CD44+ population. MWA and Western blotting assay revealed that protein expression of CD44, YAP, CYR61, CTGF, phospho-ERK1/2 T202/Y204, ERK and vimentin was elevated in PC/DX25 cells. Knockdown of CD44 or YAP suppressed migration and invasion of PC/DX25 and DU/DX50 cells. Knockdown of CD44 decreased expression of YAP, CTGF and CYR61 but increased phosphorylation of S127 on YAP. CD44 knockdown also suppressed protein level of AKT, phospho-AKT T308, phospho-ERK1/2 T202/Y204 and vimentin. CD44 promotes migration and invasion of docetaxel-resistant PCa cells probably via induction of Hippo-Yap signaling pathway and CD44/YAP pathway may be a therapeutic target for docetaxel-resistant PCa.
接受多西紫杉醇治疗的患者在几个月内产生了耐药性。我们分别从 PC-3 和 DU-145 PCa 细胞中生成了多西紫杉醇耐药的 PC/DX25 和 DU/DX50 CRPC 细胞。我们研究了 PC/DX25 和 DU/DX50 细胞表现出更高迁移和侵袭能力的机制。Transwell 测定用于测量 PCa 细胞的迁移和侵袭。荧光激活细胞分选(FACS)分析用于确定癌症干细胞(CSC)样细胞的群体。微西方阵列(MWA)用于研究蛋白质谱的变化。FACS 分析显示 PC/DX25 细胞和 DU/DX50 细胞含有更高的 CD44+群体。MWA 和 Western blot 分析显示,CD44、YAP、CYR61、CTGF、磷酸化 ERK1/2 T202/Y204、ERK 和波形蛋白的蛋白表达在 PC/DX25 细胞中升高。CD44 或 YAP 的敲低抑制了 PC/DX25 和 DU/DX50 细胞的迁移和侵袭。CD44 敲低降低了 YAP、CTGF 和 CYR61 的表达,但增加了 YAP 上 S127 的磷酸化。CD44 敲低还抑制了 AKT、磷酸化 AKT T308、磷酸化 ERK1/2 T202/Y204 和波形蛋白的蛋白水平。CD44 可能通过诱导 Hippo-Yap 信号通路促进多西紫杉醇耐药 PCa 细胞的迁移和侵袭,CD44/YAP 通路可能是多西紫杉醇耐药 PCa 的治疗靶点。