Shin Dong-Won, Kwon Yeo-Jung, Ye Dong-Jin, Baek Hyoung-Seok, Lee Joo-Eun, Chun Young-Jin
College of Pharmacy, Chung-Ang University, Seoul 06974, Republic of Korea.
Biomol Ther (Seoul). 2017 Mar 1;25(2):177-185. doi: 10.4062/biomolther.2016.223.
Auranofin has been developed as antirheumatic drugs, which is currently under clinical development for the treatment of chronic lymphocytic leukemia. Previous report showed that auranofin induced apoptosis by enhancement of annexin A5 expression in PC-3 cells. To understand the role of annexin A5 in auranofin-mediated apoptosis, we performed microarray data analysis to study annexin A5-controlled gene expression in annexin A5 knockdown PC-3 cells. Of differentially expressed genes, plasminogen activator inhibitor (PAI)-2 was increased by annexin A5 siRNA confirmed by qRT-PCR and western blot. Treatment with auranofin decreased PAI-2 and increased annexin A5 expression as well as promoting apoptosis. Furthermore, auranofin-induced apoptosis was recovered by annexin A5 siRNA but it was promoted by PAI-2 siRNA. Interestingly, knockdown of annexin A5 rescued PAI-2 expression suppressed by auranofin. Taken together, our study suggests that induction of annexin A5 by auranofin may enhance apoptosis through suppression of PAI-2 expression in PC-3 cells.
金诺芬已被开发用作抗风湿药物,目前正处于治疗慢性淋巴细胞白血病的临床开发阶段。先前的报告显示,金诺芬通过增强PC-3细胞中膜联蛋白A5的表达诱导细胞凋亡。为了了解膜联蛋白A5在金诺芬介导的细胞凋亡中的作用,我们进行了微阵列数据分析,以研究膜联蛋白A5敲低的PC-3细胞中膜联蛋白A5控制的基因表达。在差异表达的基因中,通过qRT-PCR和蛋白质印迹证实,膜联蛋白A5 siRNA可使纤溶酶原激活物抑制剂(PAI)-2增加。用金诺芬处理可降低PAI-2并增加膜联蛋白A5的表达以及促进细胞凋亡。此外,膜联蛋白A5 siRNA可恢复金诺芬诱导的细胞凋亡,但PAI-2 siRNA可促进细胞凋亡。有趣的是,膜联蛋白A5的敲低挽救了被金诺芬抑制的PAI-2表达。综上所述,我们的研究表明,金诺芬诱导的膜联蛋白A5可能通过抑制PC-3细胞中的PAI-2表达来增强细胞凋亡。