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探索缺氧诱导因子-1(HIF-1)在早期血管生成及放疗反应中的作用。

Exploring the role of HIF-1 in early angiogenesis and response to radiotherapy.

作者信息

Dewhirst Mark W, Cao Yiting, Li Chuan Yuan, Moeller Benjamin

机构信息

Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Radiother Oncol. 2007 Jun;83(3):249-55. doi: 10.1016/j.radonc.2007.05.016. Epub 2007 Jun 8.

DOI:10.1016/j.radonc.2007.05.016
PMID:17560674
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2694841/
Abstract

The objective of this review is to examine the role that HIF-1 plays in the initiation of angiogenesis and in radiotherapy response. Although these two phenomena may at first seem unrelated, there are parallelisms to be drawn associated with the importance of reactive oxygen species in controlling the transcriptional activity of HIF-1, independently of its main driving force, hypoxia. Knowledge of the mechanisms underlying the control of HIF-1 leads to rationale for its inhibition in a range of clinical scenarios.

摘要

本综述的目的是研究缺氧诱导因子-1(HIF-1)在血管生成起始及放疗反应中所起的作用。尽管这两种现象乍一看可能并无关联,但在活性氧物种在控制HIF-1转录活性方面的重要性上存在可类比之处,这与HIF-1的主要驱动因素缺氧无关。了解HIF-1调控的潜在机制为在一系列临床情况下抑制它提供了理论依据。

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Long-term administration of a small molecular weight catalytic metalloporphyrin antioxidant, AEOL 10150, protects lungs from radiation-induced injury.长期施用一种小分子催化金属卟啉抗氧化剂AEOL 10150可保护肺部免受辐射诱导的损伤。
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