Inhibiting Hedgehog: An Update on Pharmacological Compounds and Targeting Strategies

被引:25
作者
Galperin, Ilya [1 ]
Dempwolff, Lukas [2 ]
Diederich, Wibke E. [2 ,3 ]
Lauth, Matthias [1 ]
机构
[1] Philipps Univ Marburg, Ctr Tumor & Immune Biol ZTI, Hans Meerwein Str 3, D-35043 Marburg, Germany
[2] Philipps Univ Marburg, Ctr Tumor & Immune Biol ZTI, Sch Pharm, Hans Meerwein Str 3, D-35043 Marburg, Germany
[3] Philipps Univ Marburg, Core Facil Med Chem, Hans Meerwein Str 3, D-35043 Marburg, Germany
关键词
SMALL-MOLECULE INHIBITORS; GLI TRANSCRIPTION FACTORS; GROWTH-FACTOR-BETA; PATHWAY INHIBITOR; SIGNALING PATHWAY; CHOLESTEROL MODIFICATION; INDUCED APOPTOSIS; STRUCTURAL BASIS; DRUG-RESISTANCE; BINDING-SITES;
D O I
10.1021/acs.jmedchem.9b00188
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Important steps in embryonic development are governed by the Hedgehog (Hh) signaling pathway, an evolutionary conserved signal transduction cascade. However, Hh activity not only is crucial during embryo formation but also is involved in adult tissue repair and in several malignancies. Particularly due to its link to cancer, small molecule Hh pathway inhibitors have been developed and the first compounds have been approved for use in Hh-driven basal cell carcinoma. Almost all advanced Hh inhibitors target the critical signaling component Smoothened (SMO), but preclinical research has identified additional compounds that can block the Hh pathway along its entire signaling cascade, which, in light of emerging drug resistance occurring with SMO inhibitors, is of high importance. Herein we give an overview on currently known Hh pathway inhibitors, delineating their respective strengths and weaknesses and describing potential drug targeting strategies to interfere with Hh signaling in different cancer settings.
引用
收藏
页码:8392 / 8411
页数:20
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