Prodrug AST-003 Improves the Therapeutic Index of the Multi-Targeted Tyrosine Kinase Inhibitor Sunitinib

被引:6
|
作者
Huang, Qiang [1 ,2 ]
Zhou, Changhua [1 ,2 ]
Chen, Xiao [1 ]
Dong, Bing [1 ,2 ]
Chen, Siqi [1 ,2 ]
Zhang, Ning [3 ]
Liu, Yawei [4 ]
Li, Anrong [5 ]
Yao, Meicun [1 ]
Miao, Ji [1 ]
Li, Qing [1 ,2 ]
Wang, Zhong [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510275, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Ctr Cellular & Struct Biol, Guangzhou 510275, Guangdong, Peoples R China
[3] Peking Univ, Canc Hosp, Beijing Inst Canc Res, Beijing 100871, Peoples R China
[4] Gen Staff Dept PLA, Hlth Div, Guard Bur, Beijing, Peoples R China
[5] Ascenta Pharmaceut, Guangzhou, Guangdong, Peoples R China
来源
PLOS ONE | 2015年 / 10卷 / 10期
关键词
SIGNALING PATHWAYS; IN-VIVO; ANGIOGENESIS; APOPTOSIS;
D O I
10.1371/journal.pone.0141395
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Patients have responded well to the multi-targeted tyrosine kinase inhibitor (TKI) Sunitinib in the clinic. But the severe toxic side effects associated with Sunitinib limit its therapeutic index. To improve the therapeutic index of Sunitinib, a prodrug strategy was employed to modify Sunitinib. The inactive prodrug AST-003 can be converted to Sunitinib in vitro and in vivo. Compared with Sunitinib, AST-003 has unique biochemical, cellular and pharmacokinetic properties with improved tolerability in mice and yield higher efficacy in tumor xenograft models. This prodrug strategy may constitute a novel paradigm to improve the therapeutic index of Sunitinib and other TKI or anti-angiogenesis drugs in general.
引用
收藏
页数:14
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