Novel harmine derivatives for tumor targeted therapy

被引:36
作者
Li, Siwen [1 ]
Wang, Aqin [1 ]
Gu, Fan [1 ]
Wang, Zhaohui [1 ]
Tian, Caiping [1 ]
Qian, Zhiyu [2 ]
Tang, Liping [3 ]
Gu, Yueqing [1 ]
机构
[1] China Pharmaceut Univ, Sch Life Sci & Technol, State Key Lab Nat Med, Dept Biomed Engn, Arlington, TX 76019 USA
[2] Nanjing Univ Aeronaut & Astronaut, Sch Automat, Dept Biomed Engn, Nanjing, Jiangsu, Peoples R China
[3] Univ Texas Arlington, Dept Bioengn, Arlington, TX 76019 USA
关键词
harmine; structural modification; 2DG; met; tumor targeting therapy; BETA-CARBOLINE DERIVATIVES; BIOLOGICAL EVALUATION; CYTOTOXIC ACTIVITIES; ANTITUMOR-ACTIVITY; CANCER CELLS; IN-VIVO; AGENTS; DNA;
D O I
10.18632/oncotarget.3276
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Harmine is a beta-carboline alkaloid found in medicinal plant PeganumHarmala, which has served as a folk anticancer medicine. However, clinical applications of harmine were limited by its low pharmacological effects and noticeable neurotoxicity. In this study, we modified harmine to increase the therapeutic efficacy and to decrease the systemic toxicity. Specifically, two tumor targeting harmine derivatives 2DG-Har-01 and MET-Har-02 were synthesized by modifying substituent in position-2, -7 and -9 of harmine ring with two different targeting group2-amino-2-deoxy-D-glucose (2DG) and Methionine (Met), respectively. Their therapeutic efficacy and toxicity were investigated both in vitro and in vivo. Results suggested that the two newharmine derivatives displayed much higher therapeutic effects than non-modified harmine. In particular, MET-Har-02 was more potent than 2DG-Har-01 with promising potential for targeted cancer therapy.
引用
收藏
页码:8988 / 9001
页数:14
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