Hypoxia-Directed Drug Strategies to Target the Tumor Microenvironment

被引:18
作者
Hay, Michael P. [1 ]
Hicks, Kevin O. [1 ]
Wang, Jingli [1 ]
机构
[1] Univ Auckland, Auckland Canc Soc Res Ctr, Auckland 1142, New Zealand
来源
TUMOR MICROENVIRONMENT AND CELLULAR STRESS: SIGNALING, METABOLISM, IMAGING, AND THERAPEUTIC TARGETS | 2014年 / 772卷
关键词
Hypoxia; Drug discovery; Nitroimidazole; Radiosensitizer; Hypoxia-activated prodrug; Biomarker; Tirapazamine; SN30000; HIF-1; alpha; Glucose transport; PHASE-III TRIAL; SELECTIVE ANTITUMOR AGENTS; DEPENDENT PROTEIN-KINASE; SQUAMOUS-CELL CARCINOMA; BIOREDUCTIVE PRODRUG PR-104A; TIRAPAZAMINE PLUS CISPLATIN; INDUCIBLE FACTOR-1-ALPHA PROTEIN; HOMOLOGOUS RECOMBINATION REPAIR; LOCOREGIONALLY ADVANCED HEAD; LOCALLY ADVANCED HEAD;
D O I
10.1007/978-1-4614-5915-6_6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypoxia is an important component of the tumor microenvironment and has been the target of drug discovery efforts for almost half a century. These efforts have evolved from offsetting the impact of hypoxia on radiotherapy with oxygen-mimetic radiosensitizers to using hypoxia as a means to selectively target tumors. The more recent description of hypoxia-inducible factors and their role in the hypoxia response network has revealed a host of new drug targets to selectively target tumors. We are developing hypoxia-directed drugs in each of the following areas: novel radiosensitizers for hypofractionated radiotherapy, a second-generation benzotriazine di-N-oxide hypoxia-activated prodrug, and a hypoxia-inducible factor-1-dependent cytotoxin that targets glucose transport. These projects are discussed in the context of hypoxia-directed drug discovery.
引用
收藏
页码:111 / 145
页数:35
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