Targeting hypoxia in cancer therapy

被引:2572
作者
Wilson, William R. [1 ]
Hay, Michael P. [1 ]
机构
[1] Univ Auckland, Auckland Canc Soc, Res Ctr, Auckland 1, New Zealand
关键词
UNFOLDED PROTEIN RESPONSE; CARBONIC-ANHYDRASE-IX; NITRIC-OXIDE SYNTHASE; SELECTIVE ANTITUMOR AGENTS; TUMOR HYPOXIA; METABOLIC-ACTIVATION; MITOMYCIN-C; BIOREDUCTIVE DRUGS; DNA-REPAIR; HOMOLOGOUS RECOMBINATION;
D O I
10.1038/nrc3064
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypoxia is a feature of most tumours, albeit with variable incidence and severity within a given patient population. It is a negative prognostic and predictive factor owing to its multiple contributions to chemoresistance, radioresistance, angiogenesis, vasculogenesis, invasiveness, metastasis, resistance to cell death, altered metabolism and genomic instability. Given its central role in tumour progression and resistance to therapy, tumour hypoxia might well be considered the best validated target that has yet to be exploited in oncology. However, despite an explosion of information on hypoxia, there are still major questions to be addressed if the long-standing goal of exploiting tumour hypoxia is to be realized. Here, we review the two main approaches, namely bioreductive prodrugs and inhibitors of molecular targets upon which hypoxic cell survival depends. We address the particular challenges and opportunities these overlapping strategies present, and discuss the central importance of emerging diagnostic tools for patient stratification in targeting hypoxia.
引用
收藏
页码:393 / 410
页数:18
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