Ho Quoc T, Kuo Calvin J
Division of Hematology, Stanford University School of Medicine, 269 Campus Drive, Stanford, CA 94305, USA.
Int J Biochem Cell Biol. 2007;39(7-8):1349-57. doi: 10.1016/j.biocel.2007.04.010. Epub 2007 Apr 22.
While the development of anti-angiogenic therapy, as it pertains to cancer treatment, may still be in its infancy relative to well-established modalities such as chemotherapy, radiation, and surgery, major strides made in the past several decades have allowed translation of basic science discoveries in this field into clinical reality. The discovery of key molecular modulators of angiogenesis, notably vascular endothelial growth factor (VEGF), has catalyzed the development of numerous neutralizing therapeutic agents. The validity of VEGF inhibition as a therapeutic strategy has been well supported in randomized clinical trials, as well as U.S. Food and Drug Administration approval of the VEGF antagonists bevacizumab, sunitinib malate, sorafenib, pegaptinib and ranibizumab. Accordingly, this review will (1) briefly review the basic molecular biology of VEGF and (2) summarize recent progress in targeting the VEGF molecular pathway as therapy for angiogenic diseases such as cancer and age-related macular degeneration.
虽然与化疗、放疗和手术等成熟的治疗方式相比,抗血管生成疗法在癌症治疗方面的发展可能仍处于起步阶段,但在过去几十年中取得的重大进展已使该领域的基础科学发现转化为临床实际应用。血管生成关键分子调节剂的发现,尤其是血管内皮生长因子(VEGF),催化了众多中和治疗剂的开发。VEGF抑制作为一种治疗策略的有效性在随机临床试验中得到了充分支持,同时美国食品药品监督管理局也批准了VEGF拮抗剂贝伐单抗、苹果酸舒尼替尼、索拉非尼、培加替尼和雷珠单抗。因此,本综述将(1)简要回顾VEGF的基本分子生物学,(2)总结靶向VEGF分子途径作为癌症和年龄相关性黄斑变性等血管生成性疾病治疗方法的最新进展。