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血管生成抑制剂:当前策略与未来前景。

Angiogenesis inhibitors: current strategies and future prospects.

作者信息

Cook Kristina M, Figg William D

机构信息

Molecular Pharmacology Section, Medical Oncology Branch and Affiliates, National Cancer Institute, National Institutes of Health, 10 Center Drive, 9000 Rockville Pike, Bethesda, MD 20892, USA.

出版信息

CA Cancer J Clin. 2010 Jul-Aug;60(4):222-43. doi: 10.3322/caac.20075. Epub 2010 Jun 16.

Abstract

Angiogenesis has become an attractive target for drug therapy because of its key role in tumor growth. An extensive array of compounds is currently in preclinical development, with many now entering the clinic and/or achieving approval from the US Food and Drug Administration. Several regulatory and signaling molecules governing angiogenesis are of interest, including growth factors (eg, vascular endothelial growth factor, platelet-derived growth factor, fibroblast growth factor, and epidermal growth factor), receptor tyrosine kinases, and transcription factors such as hypoxia inducible factor, as well as molecules involved in mitogen-activated protein kinase (MAPK) and phosphoinositide 3-kinase (PI3K) signaling. Pharmacologic agents have been identified that target these pathways, yet for some agents (notably thalidomide), an understanding of the specific mechanisms of antitumor action has proved elusive. The following review describes key molecular mechanisms and novel therapies that are on the horizon for antiangiogenic tumor therapy.

摘要

由于血管生成在肿瘤生长中起关键作用,它已成为药物治疗的一个有吸引力的靶点。目前有大量化合物正处于临床前开发阶段,许多化合物现已进入临床和/或获得美国食品药品监督管理局的批准。几种调控血管生成的调节分子和信号分子备受关注,包括生长因子(如血管内皮生长因子、血小板衍生生长因子、成纤维细胞生长因子和表皮生长因子)、受体酪氨酸激酶,以及诸如缺氧诱导因子等转录因子,还有参与丝裂原活化蛋白激酶(MAPK)和磷脂酰肌醇3激酶(PI3K)信号传导的分子。已经确定了针对这些途径的药物制剂,但对于一些药物(尤其是沙利度胺),其抗肿瘤作用的具体机制仍难以捉摸。以下综述描述了抗血管生成肿瘤治疗即将出现的关键分子机制和新疗法。

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