Clinical Research Institute, The Second Affiliated Hospital, University of South China, Hengyang 421001, China.
College of Nursing, Hunan Polytechnic of Environment and Biology, Hengyang 421005, China.
Biomed Res Int. 2017;2017:4101653. doi: 10.1155/2017/4101653. Epub 2017 Jun 6.
Salinomycin is an antibiotic isolated from that selectively kills cancer stem cells (CSCs). However, the antitumor mechanism of salinomycin is unclear. This study investigated the chemotherapeutic efficacy of salinomycin in human prostate cancer PC-3 cells. We found that cytotoxicity of salinomycin to PC-3 cells was stronger than to nonmalignant prostate cell RWPE-1, and exposure to salinomycin induced G2/M phage arrest and apoptosis of PC-3 cells. A mechanistic study found salinomycin suppressed Wnt/-catenin pathway to induce apoptosis of PC-3 cells. An in vivo experiment confirmed that salinomycin suppressed tumorigenesis in a NOD/SCID mice xenograft model generated from implanted PC-3 cells by inhibiting the Wnt/-catenin pathway, since the total -catenin protein level was reduced and the downstream target c-Myc level was significantly downregulated. We also showed that salinomycin, but not paclitaxel, triggered more apoptosis in aldehyde dehydrogenase- (ALDH-) positive PC-3 cells, which were considered as the prostate cancer stem cells, suggesting that salinomycin may be a promising chemotherapeutic to target CSCs. In conclusion, this study suggests that salinomycin reduces resistance and relapse of prostate tumor by killing cancer cells as well as CSCs.
沙利霉素是一种从 中分离出来的抗生素,它能选择性地杀死癌症干细胞 (CSCs)。然而,沙利霉素的抗肿瘤机制尚不清楚。本研究探讨了沙利霉素对人前列腺癌 PC-3 细胞的化疗疗效。我们发现沙利霉素对 PC-3 细胞的细胞毒性强于非恶性前列腺细胞 RWPE-1,并且暴露于沙利霉素诱导了 PC-3 细胞的 G2/M 期阻滞和凋亡。一项机制研究发现,沙利霉素通过抑制 Wnt/-catenin 通路诱导 PC-3 细胞凋亡。体内实验证实,沙利霉素通过抑制 Wnt/-catenin 通路抑制了植入 PC-3 细胞的 NOD/SCID 小鼠异种移植模型中的肿瘤发生,因为总 -catenin 蛋白水平降低,下游靶标 c-Myc 水平显著下调。我们还表明,沙利霉素而非紫杉醇可引发更多的醛脱氢酶- (ALDH-)阳性 PC-3 细胞凋亡,这些细胞被认为是前列腺癌干细胞,表明沙利霉素可能是一种有前途的针对 CSCs 的化疗药物。总之,本研究表明,沙利霉素通过杀死癌细胞和 CSCs 降低了前列腺肿瘤的耐药性和复发率。