Quassinoid Inhibition of AP-1 Function Does Not Correlate with Cytotoxicity or Protein Synthesis Inhibition

被引:24
作者
Beutler, John A. [1 ]
Kang, Moon-Il [2 ]
Robert, Francis [3 ]
Clement, Jason A. [1 ]
Pelletier, Jerry [3 ]
Colburn, Nancy H. [2 ]
McKee, Tawnya C. [1 ]
Goncharova, Ekaterina [1 ,4 ]
McMahon, James B. [1 ]
Henrich, Curtis J. [1 ,5 ]
机构
[1] Natl Canc Inst, Mol Targets Dev Program, Frederick, MD 21702 USA
[2] Natl Canc Inst, Lab Canc Prevent, Ctr Canc Res, Frederick, MD 21702 USA
[3] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[4] Data Management Serv Inc, Frederick, MD 21702 USA
[5] SAIC Frederick Inc, Basic Res Program, NCI Frederick, Frederick, MD 21702 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2009年 / 72卷 / 03期
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; ANTI-CANCER AGENTS; CONSTITUENTS; BRUCEANTIN; SIMAROUBACEAE; ACTIVATION; PROMOTION; TARGETS; MODE;
D O I
10.1021/np800732n
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Several quassinoids were identified in a high-throughput screening assay as inhibitors of the transcription factor AP-1. Further biological characterization revealed that while their effect was not specific to AP-1, protein synthesis inhibition and cell growth assays were inconsistent with a mechanism of simple protein synthesis inhibition. Numerous plant extracts from the plant family Simaroubaceae were also identified in the same screen; bioassay-guided fractionation of one extract (Ailanthus triphylla) yielded two known quassinoids, ailanthinone (3) and glaucarubinone (4), which were also identified in the pure compound screening procedure.
引用
收藏
页码:503 / 506
页数:4
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