Hypoxia-Inducible Factor-1 (HIF-1)-Active Cells as a Target for Cancer Therapy

被引:11
|
作者
Kizaka-Kondoh, Shinae [1 ]
Kuchimaru, Takahiro [1 ]
Kadonosono, Tetsuya [1 ]
机构
[1] Tokyo Inst Technol, Grad Sch Biosci & Biotechnol, Dept Biomol Engn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
关键词
hypoxia-inducible factor (HIF); protein transduction domain; oxygen-dependent degradation; bioluminescence imaging; pancreatic cancer; PROLYL HYDROXYLATION; TUMOR XENOGRAFTS; HIF-ALPHA; PROTEIN; MOUSE; HYPOXIA-INDUCIBLE-FACTOR-1-ALPHA; ANGIOGENESIS; DESTRUCTION; HIF-1-ALPHA; EXPRESSION;
D O I
10.1254/jphs.10R20FM
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The microenvironment of solid tumors is characterized by low pO(2) that is well below physiological levels. Intratumoral hypoxia is a major factor contributing to cancer progression and is exacerbated as a result of oxygen consumption by rapidly proliferating tumor cells near blood vessels, poor lymphatic drainage resulting in high interstitial pressure, and irregular blood supply through immature tumor vasculature. Hypoxia-inducible factor-1 (HIF-1) is the main transcription factor that regulates cellular responses to hypoxia. Cellular changes induced by HIF-1 are extremely important targets for cancer therapy. Therefore, targeting strategies to counteract HIF-1-active cells are essential for cancer therapy. In this study, we introduce a novel strategy for targeting HIF-1-active cells.
引用
收藏
页码:440 / 445
页数:6
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