Hh signaling inhibitors from Vitex negundo; naturally occurring inhibitors of the GLI1-DNA complex

被引:30
作者
Arai, Midori A. [1 ]
Fujimatsu, Teruhisa [1 ]
Uchida, Kyoko [1 ]
Sadhu, Samir K. [2 ]
Ahmed, Firoj [3 ]
Ishibashi, Masami [1 ]
机构
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Chuo Ku, Chiba 2608675, Japan
[2] Khulna Univ, Pharm Discipline, Sch Life Sci, Khulna 9208, Bangladesh
[3] Jagannath Univ, Dept Pharm, Dhaka 1100, Bangladesh
基金
日本学术振兴会;
关键词
SMALL-MOLECULE INHIBITORS; HEDGEHOG PATHWAY; MEDIATED TRANSCRIPTION; BINDING-SITE; CANCER; DITERPENES; TRANSDUCTION; CYCLOPAMINE; EXPRESSION; GLYCOSIDE;
D O I
10.1039/c3mb25567k
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The hedgehog (Hh) signaling pathway has crucial roles in embryonic development, cell maintenance and proliferation, and is also known to contribute to cancer cell growth. New naturally occurring Hh inhibitors (1, 7 and 9) were isolated from Vitex negundo using our previously constructed cell-based assay. Bioactivity guided isolation provided 9 natural compounds including a new diterpene, nishindanol (9). Compounds 7 and 9 showed cytotoxicity against cancer cell lines in which Hh signaling was aberrantly activated. Vitetrifolin D (7; GLI1 transcriptional inhibition IC50 = 20.2 mu M) showed inhibition of Hh related protein (PTCH and BCL2) production. Interestingly, the constructed electrophoresis mobility shift assay revealed that vitetrifolin D (7) disrupted GLI1 binding on its DNA binding domain. epi-Sclareol (8; inactive), possessing a similar structure to 7, did not show inhibition of GLI1-DNA complex formation. This is the first example of naturally occurring inhibitors of GLI1-DNA complex formation.
引用
收藏
页码:1012 / 1018
页数:7
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