Arsenic Sulfide Promotes Apoptosis in Retinoid Acid Resistant Human Acute Promyelocytic Leukemic NB4-R1 Cells through Downregulation of SET Protein

作者：Tian, Yuwang; Liu, Yanfeng; He, Pengcheng^*; Liu, Feng; Zhou, Naicen; Cheng, Xiaoyan; Shi, Lili; Zhu, Huachao; Zhao, Jing; Wang, Yuan; Zhang, Mei

来源：PLos One, 2014, 9(1): e83184.

DOI：10.1371/journal.pone.0083184

• PHOSPHATASE 2A
• REALGAR NANOPARTICLES
• TRIOXIDE
• INHIBITOR
• EXPRESSION
• MANAGEMENT
• FUSION
• GROWTH
• PP2A
• ATRA

Tetra-arsenic tetra-sulfide (As4S4) is an arsenic compound with anti-tumor activity, especially in acute promyelocytic leukemia (APL) that are resistant to retinoic acid (RA). Although recent studies revealed that the therapeutic action of As4S4 is closely associated with the induction of cellular apoptosis, the exact molecular mechanism of action of As4S4 in RA-resistant APL remains to be clarified. In this study, we found that As4S4-induced apoptosis was accompanied by reduced mRNA and protein expression of SET gene in RA-resistant NB4-R1 cells. Moreover, RNAi knockdown of SET gene further promoted As4S4-induced apoptosis, while SET over-expression inhibited it, suggesting that As4S4 induces apoptosis through the reduction of SET protein in NB4-R1 cells. We also demonstrated that the knockdown of SET gene resulted in the upregulation of protein phosphatase 2 (PP2A) expression and the downregulation of promyelocytic leukemia and retinoic acid receptor alpha fusion gene (PML-RAR alpha) expression, which were enhanced by As4S4 treatments. By contrast, over-expression of SET gene resulted in PP2A downregulation and PML-RAR alpha upregulation, which were abolished by As4S4 pretreatment. Since PP2A is a pro-apoptotic factor and PMLRAR alpha is an anti-apoptotic factor, our results suggest that As4S4-induced apoptosis in NB4-R1 cells is through the downregulation of SET protein expression, which in turn increases PP2A and reduces PML-RAR alpha expressions to lead to cell apoptosis.

• 出版日期2014-1-13
• 单位西安交通大学