肿瘤血管生成中缺氧诱导因子-1非依赖途径

Hypoxia inducible factor-1 independent pathways in tumor angiogenesis.

作者信息

Mizukami Yusuke, Kohgo Yutaka, Chung Daniel C

机构信息

Division of Gastroenterology and Hematology/Oncology, Department of Medicine, Asahikawa Medical College, Asahikawa, Hokkaido, Japan.

出版信息

Clin Cancer Res. 2007 Oct 1;13(19):5670-4. doi: 10.1158/1078-0432.CCR-07-0111.

Abstract

Among the factors that can stimulate angiogenesis, vascular endothelial growth factor has emerged as one of the most important, and inhibition of vascular endothelial growth factor has recently shown efficacy in the treatment of advanced colorectal cancer. Hypoxia develops within solid tumors and is one of the most potent stimuli of vascular endothelial growth factor expression. This effect is mediated primarily by hypoxia inducible factor-1 (HIF-1), often considered a master regulator of angiogenesis in hypoxia. Consequently, inhibition of HIF-1 has been proposed as a strategy to block tumor angiogenesis therapeutically. However, accumulating evidence indicates that HIF-independent pathways can also control angiogenesis. This review highlights some of the key signaling pathways independent of HIF-1 that can stimulate angiogenesis in hypoxia. Understanding the full spectrum of molecular pathways that control tumor angiogenesis is critical for the optimal design of targeted therapies.

摘要

在能够刺激血管生成的诸多因素中,血管内皮生长因子已成为最重要的因素之一,并且抑制血管内皮生长因子最近已在晚期结直肠癌的治疗中显示出疗效。实体瘤内部会出现缺氧情况,这是血管内皮生长因子表达的最有力刺激因素之一。这种效应主要由缺氧诱导因子-1(HIF-1)介导,HIF-1通常被认为是缺氧状态下血管生成的主要调节因子。因此,抑制HIF-1已被提议作为一种治疗性阻断肿瘤血管生成的策略。然而,越来越多的证据表明,不依赖HIF-1的途径也能够控制血管生成。本综述重点介绍了一些不依赖HIF-1的关键信号通路,这些通路在缺氧情况下能够刺激血管生成。了解控制肿瘤血管生成的全部分子途径对于靶向治疗的优化设计至关重要。

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