中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Discovery of Novel Macrocyclic Hedgehog Pathway Inhibitors Acting by Suppressing the Gli-Mediated Transcription

文献类型:期刊论文

作者Liu, Gang1,2,3; Huang, Wenjing4; Wang, Juan4; Liu, Xiaohua2,3; Yang, Jun4; Zhang, Yu4; Geng, Yong1,2,3; Tan, Wenfu4; Zhang, Ao1,2,3,5
刊名JOURNAL OF MEDICINAL CHEMISTRY
出版日期2017-10-12
卷号60期号:19页码:8218-8245
ISSN号0022-2623
DOI10.1021/acs.jmedchem.7b01185
文献子类Article
英文摘要[GRAPHICS] A systemic medicinal chemistry campaign was conducted based on a literature hit compound 5 bearing the 4,5-dihydro-2H-benzo[b][1,5]oxazocin-6(3H)-one core through cyclization of two side substituents of the bicyclic skeleton combined with N-atom walking or ring walking and the central ring expansion or extraction approaches, leading to several series of structurally unique tricyclic compounds. Among these, compound 29a was identified as the most potent against the Hedgehog (Hh) signaling pathway showing an IC50 value of 23 nM. Mechanism studies indicated that compound 29a inhibited the Hh signaling pathway by suppressing the expression of the transcriptional factors Gli rather than by interrupting the binding of Gli with DNA. We further observed that 29a was equally potent against both Smo wild type and the two major resistant mutants (Smo D473H and Smo W535L). It potently inhibited the proliferation of medulloblastoma cells and showed significant tumor growth inhibition in the ptch +/- ;p53-/- medulloblastoma allograft mice model. Though more studies are needed to clarify the precise interaction pattern of 29a with Gli, its promising in vitro and in vivo properties encourage further profiling as a new generation Hh signaling inhibitor to treat tumors primarily or secondarily resistant to current Smo inhibitors.
WOS关键词BASAL-CELL CARCINOMA ; CANCER ; MEDULLOBLASTOMA ; GROWTH ; ACTIVATION ; RESISTANCE ; VISMODEGIB ; ANTAGONISTS ; SONIDEGIB ; STRATEGY
资助项目Chinese NSF[81773565] ; Chinese NSF[81773767] ; Chinese NSF[81430080] ; National Program on Key Basic Research Project of China[2015CB910603-004] ; International Cooperative Program[GJHZ1622] ; Frontier Science of the Chinese Academy of Sciences[160621] ; Shanghai Commission of Science and Technology[16XD1404600] ; Shanghai Commission of Science and Technology[14431900400] ; CAS Key Laboratory of Receptor Research of SIMM[SIMM1606YKF-08] ; CAS Key Laboratory of Receptor Research of SIMM[SIMM1606YZZ-06]
WOS研究方向Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000413131400020
出版者AMER CHEMICAL SOC
源URL[http://119.78.100.183/handle/2S10ELR8/272454]  
专题药理学第一研究室
中科院受体结构与功能重点实验室
新药研究国家重点实验室
药物化学研究室
通讯作者Tan, Wenfu; Zhang, Ao
作者单位1.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
2.SIMM, CAS Key Lab Receptor Res, Shanghai 201203, Peoples R China;
3.SIMM, State Key Lab Drug Res, Shanghai 201203, Peoples R China;
4.Fudan Univ, Dept Pharmacol, Sch Pharm, Shanghai 201203, Peoples R China;
5.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China;
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GB/T 7714
Liu, Gang,Huang, Wenjing,Wang, Juan,et al. Discovery of Novel Macrocyclic Hedgehog Pathway Inhibitors Acting by Suppressing the Gli-Mediated Transcription[J]. JOURNAL OF MEDICINAL CHEMISTRY,2017,60(19):8218-8245.
APA Liu, Gang.,Huang, Wenjing.,Wang, Juan.,Liu, Xiaohua.,Yang, Jun.,...&Zhang, Ao.(2017).Discovery of Novel Macrocyclic Hedgehog Pathway Inhibitors Acting by Suppressing the Gli-Mediated Transcription.JOURNAL OF MEDICINAL CHEMISTRY,60(19),8218-8245.
MLA Liu, Gang,et al."Discovery of Novel Macrocyclic Hedgehog Pathway Inhibitors Acting by Suppressing the Gli-Mediated Transcription".JOURNAL OF MEDICINAL CHEMISTRY 60.19(2017):8218-8245.

入库方式: OAI收割

来源:上海药物研究所

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