Bioreductive prodrugs as cancer therapeutics: targeting tumor hypoxia

被引:132
作者
Guise, Christopher P. [1 ]
Mowday, Alexandra M. [1 ]
Ashoorzadeh, Amir [1 ]
Yuan, Ran [2 ]
Lin, Wan-Hua [2 ]
Wu, Dong-Hai [2 ]
Smaill, Jeff B. [1 ]
Patterson, Adam V. [1 ]
Ding, Ke [2 ]
机构
[1] Univ Auckland, Sch Med Sci, Auckland Canc Soc Res Ctr, Auckland 1142, New Zealand
[2] Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, Key Lab Regenerat Biol, Guangzhou 510530, Guangdong, Peoples R China
关键词
Bioreductive; prodrug; tumor hypoxia; clinical trial; oxidoreductase; CELL LUNG-CANCER; RADIATION ONCOLOGY GROUP; DT-DIAPHORASE ACTIVITY; DNA CROSS-LINKING; C P450 REDUCTASE; PHASE-III TRIAL; ACTIVATED PRODRUG; MITOMYCIN-C; SOLID TUMORS; RELATIVE IMPORTANCE;
D O I
10.5732/cjc.012.10285
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypoxia, a state of low oxygen, is a common feature of solid tumors and is associated with disease progression as well as resistance to radiotherapy and certain chemotherapeutic drugs. Hypoxic regions in tumors, therefore, represent attractive targets for cancer therapy. To date, five distinct classes of bioreactive prodrugs have been developed to target hypoxic cells in solid tumors. These hypoxia-activated prodrugs, including nitro compounds, N-oxides, quinones, and metal complexes, generally share a common mechanism of activation whereby they are reduced by intracellular oxidoreductases in an oxygen-sensitive manner to form cytotoxins. Several examples including PR-104, TH-302, and EO9 are currently undergoing phase II and phase III clinical evaluation. In this review, we discuss the nature of tumor hypoxia as a therapeutic target, focusing on the development of bioreductive prodrugs. We also describe the current knowledge of how each prodrug class is activated and detail the clinical progress of leading examples.
引用
收藏
页码:80 / 86
页数:7
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