SF002-96-1, a new drimane sesquiterpene lactone from an Aspergillus species, inhibits survivin expression

被引:22
作者
Felix, Silke [1 ]
Sandjo, Louis P. [2 ]
Opatz, Till [2 ]
Erkel, Gerhard [3 ]
机构
[1] Inst Biotechnol & Drug Res IBWF, D-67663 Kaiserslautern, Germany
[2] Johannes Gutenberg Univ Mainz, Inst Organ Chem, D-55128 Mainz, Germany
[3] Univ Kaiserslautern, Dept Mol Biotechnol & Syst Biol, D-67663 Kaiserslautern, Germany
关键词
apoptosis; inhibitor; natural products; secondary metabolite; structure elucidation; survivin; CHROMOSOMAL PASSENGER COMPLEX; BREAST-CANCER CELLS; NF-KAPPA-B; GENE-EXPRESSION; TARGETING SURVIVIN; APOPTOSIS; PATHWAY; ACTIVATION; NUCLEAR; MITOSIS;
D O I
10.3762/bjoc.9.323
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Survivin, a member of the IAP (inhibitor of apoptosis) gene family, is overexpressed in virtually all human cancers and is functionally involved in the inhibition of apoptosis, regulation of cell proliferation, metastasis and resistance to therapy. Because of its upregulation in malignancy, survivin has currently attracting considerable interest as a new target for anticancer therapy. In a screening of approximately 200 strains of imperfect fungi for the production of inhibitors of survivin promoter activity, a new drimane sesquiterpene lactone, SF002-96-1, was isolated from fermentations of an Aspergillus species. The compound inhibited survivin promoter activity in transiently transfected Colo 320 cells in a dose dependent manner with IC50 values of 3.42 mu M (1.3 mu g/mL). Moreover, it also reduced mRNA levels and protein synthesis of survivin and triggered apoptosis.
引用
收藏
页码:2866 / 2876
页数:11
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