急性早幼粒细胞白血病
细胞凋亡
髓系白血病
癌症研究
药理学
白血病
生物
伯氨喹
维甲酸
维甲酸
细胞培养
免疫学
生物化学
疟疾
氯喹
遗传学
作者
Lan Ma,Lianjuan Chen,Haoying Li,Lu Ge,Siheng Wang,Zhida Zhang,He Huang,Liuzhi Shi,Tong Li,Haihua Gu,Jianxin Lyu,Licai He
标识
DOI:10.1002/jlb.3a0120-061rr
摘要
As a subtype of acute myeloid leukemia (AML), acute promyelocytic leukemia (APL) is characterized by a chromosomal translocation, most of which result in the production of a PML-RAR alpha fusion protein. Although the overall survival rate of APL patients has improved dramatically due to all-trans retinoic acid (ATRA) treatment, ATRA-resistance remains a clinical challenge in the management of APL. Therefore, alternative agents should be considered for ATRA-resistant APL patients. Here, we report that antimalaria drug primaquine phosphate (PRQ) exhibits an anti-leukemia effect on both ATRA-sensitive cell line NB4 and ATRA-resistant APL cell lines, NB4-LR2, NB4-LR1, and NB4-MR2. Moreover, PRQ significantly inhibited primary colony formation of untreated or relapsed APL patients. Further study showed that PRQ could induce the apoptosis of APL cells by inhibiting NF-κB signaling pathway. The in vivo study showed that PRQ significantly inhibited NB4-LR2 xenograft tumors growth. These results suggest that PRQ is a potential therapeutic agent for ATRA-resistant APL patients.
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