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Polymeric nanoparticle-encapsulated hedgehog pathway inhibitor HPI-1 (NanoHHI) inhibits systemic metastases in an orthotopic model of human hepatocellular carcinoma.聚合物纳米颗粒包裹的 hedgehog 通路抑制剂 HPI-1(NanoHHI)抑制了人肝癌原位模型中的系统性转移。
Clin Cancer Res. 2012 Mar 1;18(5):1291-302. doi: 10.1158/1078-0432.CCR-11-0950. Epub 2011 Aug 25.
2
Hedgehog signaling and pancreatic tumor development.刺猬信号通路与胰腺肿瘤的发生发展。
Adv Cancer Res. 2011;110:1-17. doi: 10.1016/B978-0-12-386469-7.00001-3.
3
The miR-143/145 cluster is a novel transcriptional target of Jagged-1/Notch signaling in vascular smooth muscle cells.miR-143/145 簇是血管平滑肌细胞中 Jagged-1/Notch 信号的一个新的转录靶标。
J Biol Chem. 2011 Aug 12;286(32):28312-21. doi: 10.1074/jbc.M111.221945. Epub 2011 Jun 17.
4
Role of Jagged1 in arterial lesions after vascular injury.Jagged1 在血管损伤后动脉病变中的作用。
Arterioscler Thromb Vasc Biol. 2011 Sep;31(9):2000-6. doi: 10.1161/ATVBAHA.111.225144. Epub 2011 Jun 16.
5
Notch signaling as a therapeutic target for breast cancer treatment? Notch 信号通路作为乳腺癌治疗的治疗靶点?
Breast Cancer Res. 2011 May 31;13(3):210. doi: 10.1186/bcr2875.
6
Current status of therapeutic targeting of developmental signalling pathways in oncology.肿瘤治疗中发育信号通路的治疗靶向的现状。
Curr Pharm Biotechnol. 2012 Sep;13(11):2184-220. doi: 10.2174/138920112802502114.
7
Glycogen synthase kinase 3 beta positively regulates Notch signaling in vascular smooth muscle cells: role in cell proliferation and survival.糖原合酶激酶 3β正向调节血管平滑肌细胞中的 Notch 信号通路:在细胞增殖和存活中的作用。
Basic Res Cardiol. 2011 Sep;106(5):773-85. doi: 10.1007/s00395-011-0189-5. Epub 2011 May 10.
8
Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease.低功能态 Notch3 等位基因将 Notch 信号与缺血性脑小血管病联系起来。
Proc Natl Acad Sci U S A. 2011 May 24;108(21):E128-35. doi: 10.1073/pnas.1101964108. Epub 2011 May 9.
9
Companies race to develop first Hedgehog inhibitor cancer drug.各公司竞相研发首款刺猬信号通路抑制剂抗癌药物。
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Gamma-secretase inhibitor treatment promotes VEGF-A-driven blood vessel growth and vascular leakage but disrupts neovascular perfusion.γ-分泌酶抑制剂治疗促进 VEGF-A 驱动的血管生长和血管渗漏,但破坏新血管灌注。
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研究性 Notch 和 Hedgehog 抑制剂——心血管疾病的治疗方法。

Investigational Notch and Hedgehog inhibitors--therapies for cardiovascular disease.

机构信息

University of Rochester, Department of Surgery, 601 Elmwood Ave, Box SURG, Rochester, NY 14642, USA.

出版信息

Expert Opin Investig Drugs. 2011 Dec;20(12):1649-64. doi: 10.1517/13543784.2011.628658. Epub 2011 Oct 18.

DOI:10.1517/13543784.2011.628658
PMID:22007748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3234529/
Abstract

INTRODUCTION

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.

AREAS COVERED

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.

EXPERT OPINION

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.

摘要

简介

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。

涵盖领域

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。

专家意见

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。