University of Rochester, Department of Surgery, 601 Elmwood Ave, Box SURG, Rochester, NY 14642, USA.
Expert Opin Investig Drugs. 2011 Dec;20(12):1649-64. doi: 10.1517/13543784.2011.628658. Epub 2011 Oct 18.
During the past decade, a variety of Notch and Hedgehog pathway inhibitors have been developed for the treatment of several cancers. An emerging paradigm suggests that these same gene regulatory networks are often recapitulated in the context of cardiovascular disease and may now offer an attractive target for therapeutic intervention.
This article briefly reviews the profile of Notch and Hedgehog inhibitors that have reached the preclinic and clinic for cancer treatment and discusses the clinical issues surrounding targeted use of these inhibitors in the treatment of vascular disorders.
Preclinical and clinical data using pan-Notch inhibitors (γ-secretase inhibitors) and selective antibodies to preferentially target notch receptors and ligands have proven successful but concerns remain over normal organ homeostasis and significant pathology in multiple organs. By contrast, the Hedgehog-based drug pipeline is rich with more than a dozen Smoothened (SMO) inhibitors at various stages of development. Overall, refined strategies will be necessary to harness these pathways safely as a powerful tool to disrupt angiogenesis and vascular proliferative phenomena without causing prohibitive side effects already seen with cancer models and patients.
在过去的十年中,已经开发出了多种 Notch 和 Hedgehog 通路抑制剂,用于治疗多种癌症。一个新出现的范例表明,这些相同的基因调控网络在心血管疾病的背景下经常被重现,并且现在可能为治疗干预提供了一个有吸引力的目标。
本文简要回顾了已达到癌症治疗前临床和临床阶段的 Notch 和 Hedgehog 抑制剂的概况,并讨论了围绕这些抑制剂在血管疾病治疗中的靶向应用的临床问题。
使用泛 Notch 抑制剂(γ-分泌酶抑制剂)和选择性抗体来优先靶向 notch 受体和配体的临床前和临床数据已被证明是成功的,但人们仍然担心正常器官稳态和多个器官的显著病理学。相比之下,Hedgehog 为基础的药物管道富含十几种 Smoothened(SMO)抑制剂,处于不同的开发阶段。总体而言,需要制定更精细的策略,以安全地利用这些途径作为一种强大的工具,来破坏血管生成和血管增殖现象,而不会产生已经在癌症模型和患者中看到的禁止性副作用。