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SF002-96-1,一种新型的倍半萜烯内酯,来源于曲霉属真菌,能够抑制生存素的表达。

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

机构信息

Institute of Biotechnology and Drug Research (IBWF), Erwin-Schrödinger-Straße 56, D-67663 Kaiserslautern, Germany.

Institute of Organic Chemistry, University of Mainz, Duesbergweg 10-14, D-55128 Mainz, Germany.

出版信息

Beilstein J Org Chem. 2013 Dec 13;9:2866-76. doi: 10.3762/bjoc.9.323. eCollection 2013.

Abstract

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 µM (1.3 µg/mL). Moreover, it also reduced mRNA levels and protein synthesis of survivin and triggered apoptosis.

摘要

Survivin,凋亡抑制蛋白(IAP)基因家族的一员,在几乎所有人类癌症中过表达,并在凋亡抑制、细胞增殖调控、转移和治疗耐药性方面发挥功能。由于其在恶性肿瘤中的上调,Survivin 作为一种新的抗癌治疗靶点,目前引起了相当大的兴趣。在对大约 200 株不完全真菌进行筛选以寻找 Survivin 启动子活性抑制剂的过程中,从一种曲霉属真菌的发酵产物中分离到一种新的倍半萜烯内酯 SF002-96-1。该化合物以剂量依赖的方式抑制瞬时转染的 Colo 320 细胞中的 Survivin 启动子活性,IC50 值为 3.42µM(1.3µg/mL)。此外,它还降低了 Survivin 的 mRNA 水平和蛋白质合成,并触发了细胞凋亡。

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