Liao Debbie, Johnson Randall S
Department of Molecular Pathology, University of California San Diego, San Diego, CA, USA.
Cancer Metastasis Rev. 2007 Jun;26(2):281-90. doi: 10.1007/s10555-007-9066-y.
Angiogenesis is an important mediator of tumor progression. As tumors expand, diffusion distances from the existing vascular supply increases resulting in hypoxia. Sustained expansion of a tumor mass requires new blood vessel formation to provide rapidly proliferating tumor cells with an adequate supply of oxygen and metabolites. The key regulator of hypoxia-induced angiogenesis is the transcription factor hypoxia inducible factor (HIF)-1. Multiple HIF-1 target genes have been shown to modulate angiogenesis by promoting the mitogenic and migratory activities of endothelial cells. Because of this, hypoxia-induced angiogenesis has become an attractive target for cancer therapy, however the mechanisms involved during this process and how best to target it for cancer therapy are still under investigation. This review will cover the current understanding of hypoxia-induced tumor angiogenesis and discuss the caveats of hypoxia-targeted antiangiogenic therapy for the treatment of cancer.
血管生成是肿瘤进展的重要介导因素。随着肿瘤的扩大,来自现有血管供应的扩散距离增加,导致缺氧。肿瘤块的持续扩大需要新血管形成,以为快速增殖的肿瘤细胞提供充足的氧气和代谢物供应。缺氧诱导血管生成的关键调节因子是转录因子缺氧诱导因子(HIF)-1。多个HIF-1靶基因已被证明可通过促进内皮细胞的促有丝分裂和迁移活性来调节血管生成。因此,缺氧诱导的血管生成已成为癌症治疗的一个有吸引力的靶点,然而,这一过程中涉及的机制以及如何最好地将其作为癌症治疗靶点仍在研究中。本综述将涵盖目前对缺氧诱导肿瘤血管生成的理解,并讨论缺氧靶向抗血管生成治疗癌症的注意事项。