血管生成
HIF1A型
癌症研究
缺氧(环境)
缺氧诱导因子1
转录因子
体内
血管内皮生长因子
缺氧诱导因子
调节器
癌细胞
癌症
生物
药品
肿瘤缺氧
药理学
基因
医学
内科学
化学
血管内皮生长因子受体
生物化学
遗传学
有机化学
放射治疗
氧气
作者
Garth Powis,Lynn Kirkpatrick
出处
期刊:Molecular Cancer Therapeutics
[American Association for Cancer Research]
日期:2004-05-01
卷期号:3 (5): 647-654
被引量:271
标识
DOI:10.1158/1535-7163.647.3.5
摘要
The hypoxia inducible factor 1 (HIF-1) is a heterodimeric transcription factor that is an important regulator of the growing tumor's response to hypoxia. HIF-1 activity in tumors depends on the availability of the HIF-1alpha subunit, the levels of which increase under hypoxic conditions and through the activation of oncogenes and/or inactivation of tumor suppressor genes. HIF-1 activates genes that allow the cancer cell to survive and grow in the hostile hypoxic tumor environment. Increased tumor HIF-1alpha has been correlated with increased angiogenesis, aggressive tumor growth, and poor patient prognosis, leading to the current interest in HIF-1alpha as a cancer drug target. A number of anticancer agents have been reported to decrease HIF-1alpha or HIF-1 transactivating activity in cells in culture. However, more relevant to the agents' antitumor activity is whether HIF-1 is inhibited in tumors in vivo. This has been demonstrated for only a few of the reported HIF-1 inhibitors. Some of the agents are moving toward clinical trial where it will be important to demonstrate that the agents inhibit HIF-1alpha in patient tumors or, failing this, the downstream consequences of HIF-1 inhibition such as decreased vascular endothelial growth factor formation, and relate this inhibition to antitumor activity. Only in this way will it be possible to determine if HIF-1alpha is a valid cancer drug target in humans.
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