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Fostriecin: a review of the preclinical data.

作者信息

de Jong R S, de Vries E G, Mulder N H

机构信息

Department of Internal Medicine, University Hospital Groningen, The Netherlands.

出版信息

Anticancer Drugs. 1997 Jun;8(5):413-8.

PMID:9215602
Abstract

Fostriecin is a novel antitumor antibiotic. In vitro studies showed that fostriecin inhibits DNA topoisomerase II (Topo II) catalytic activity, protein phosphatases involved with cell-cycle control and histone phosphatases. The relative contribution of these mechanisms to the antitumor activity has not been elucidated, but Topo II inhibition seems to be the major mechanism of action at in vitro cytotoxic fostriecin levels. Tumor cell lines with decreased Topo II content showed similar or increased sensitivity to fostriecin, compared to the parent cell lines. The reduced-folate carrier is probably responsible for the cellular uptake of fostriecin. The possible clinical consequences of these in vitro observations are discussed.

摘要

相似文献

1
Fostriecin: a review of the preclinical data.
Anticancer Drugs. 1997 Jun;8(5):413-8.
2
Fostriecin-mediated G2-M-phase growth arrest correlates with abnormal centrosome replication, the formation of aberrant mitotic spindles, and the inhibition of serine/threonine protein phosphatase activity.福司曲星介导的G2-M期生长停滞与中心体复制异常、异常有丝分裂纺锤体的形成以及丝氨酸/苏氨酸蛋白磷酸酶活性的抑制相关。
Cancer Res. 1998 Aug 15;58(16):3611-9.
3
Antitumor drug fostriecin inhibits the mitotic entry checkpoint and protein phosphatases 1 and 2A.抗肿瘤药物福司曲星抑制有丝分裂进入检查点以及蛋白磷酸酶1和2A。
Cancer Res. 1994 Dec 1;54(23):6115-21.
4
Lack of cross-resistance to fostriecin in a human small-cell lung carcinoma cell line showing topoisomerase II-related drug resistance.在一株显示拓扑异构酶II相关耐药性的人小细胞肺癌细胞系中对福司曲星不存在交叉耐药性。
Cancer Chemother Pharmacol. 1991;28(6):461-4. doi: 10.1007/BF00685823.
5
Phase I and pharmacokinetic study of the topoisomerase II catalytic inhibitor fostriecin.拓扑异构酶II催化抑制剂福司曲星的I期及药代动力学研究
Br J Cancer. 1999 Feb;79(5-6):882-7. doi: 10.1038/sj.bjc.6690141.
6
Antitumor antibiotic fostriecin covalently binds to cysteine-269 residue of protein phosphatase 2A catalytic subunit in mammalian cells.抗肿瘤抗生素福司曲星 c 在哺乳动物细胞中与蛋白磷酸酶 2A 催化亚基的半胱氨酸 269 残基共价结合。
Bioorg Med Chem. 2009 Dec 1;17(23):8113-22. doi: 10.1016/j.bmc.2009.09.050. Epub 2009 Oct 3.
7
Effects of DNA topoisomerase II inhibitors on human bone marrow progenitor cells.
Leukemia. 1994 Jan;8(1):121-8.
8
Catalyst-controlled asymmetric synthesis of fostriecin and 8-epi-fostriecin.催化剂控制的福司曲星和8-表福司曲星的不对称合成。
J Am Chem Soc. 2005 Dec 7;127(48):17111-7. doi: 10.1021/ja0562043.
9
Inhibition of type II topoisomerase by fostriecin.
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10
The antitumor drug fostriecin induces vimentin hyperphosphorylation and intermediate filament reorganization.抗肿瘤药物福司曲星可诱导波形蛋白过度磷酸化和中间丝重排。
Carcinogenesis. 1996 May;17(5):967-72. doi: 10.1093/carcin/17.5.967.

引用本文的文献

1
Total and Formal Syntheses of Fostriecin.福司曲星的全合成与形式合成
Org Chem Front. 2020 Nov 21;7(22):3608-3615. doi: 10.1039/d0qo01121e. Epub 2020 Oct 12.
2
Synthetic Strategies Employed for the Construction of Fostriecin and Related Natural Products.用于构建磷霉素和相关天然产物的合成策略。
Chem Rev. 2016 Dec 28;116(24):15035-15088. doi: 10.1021/acs.chemrev.6b00488. Epub 2016 Dec 8.
3
Viewing serine/threonine protein phosphatases through the eyes of drug designers.从药物设计师的视角看丝氨酸/苏氨酸蛋白磷酸酶。
FEBS J. 2013 Oct;280(19):4739-60. doi: 10.1111/febs.12481. Epub 2013 Sep 5.
4
Suppression of Ser/Thr phosphatase 4 (PP4C/PPP4C) mimics a novel post-mitotic action of fostriecin, producing mitotic slippage followed by tetraploid cell death.抑制丝氨酸/苏氨酸磷酸酶 4(PP4C/PPP4C)模拟了福司他汀的一种新的有丝分裂后作用,导致有丝分裂滑步,随后四倍体细胞死亡。
Mol Cancer Res. 2013 Aug;11(8):845-55. doi: 10.1158/1541-7786.MCR-13-0032. Epub 2013 May 13.
5
De novo synthesis of natural products via the asymmetric hydration of polyenes.通过多烯的不对称水合作用从头合成天然产物。
Chem Commun (Camb). 2011 Aug 14;47(30):8493-505. doi: 10.1039/c1cc11791b. Epub 2011 May 11.
6
Total synthesis of fostriecin: via a regio- and stereoselective polyene hydration, oxidation, and hydroboration sequence.福司替丁的全合成:通过区域和立体选择性聚烯烃水合、氧化和硼氢化反应序列。
Org Lett. 2010 Sep 3;12(17):3752-5. doi: 10.1021/ol101340n.
7
Structure-activity relationship studies of fostriecin, cytostatin, and key analogs, with PP1, PP2A, PP5, and( beta12-beta13)-chimeras (PP1/PP2A and PP5/PP2A), provide further insight into the inhibitory actions of fostriecin family inhibitors.福司曲星、细胞抑制素及关键类似物与PP1、PP2A、PP5以及(β12-β13)嵌合体(PP1/PP2A和PP5/PP2A)之间的构效关系研究,为深入了解福司曲星家族抑制剂的抑制作用提供了更多见解。
J Pharmacol Exp Ther. 2009 Oct;331(1):45-53. doi: 10.1124/jpet.109.155630. Epub 2009 Jul 10.
8
Protein phosphatase 2A enhances activation of human immunodeficiency virus type 1 by phorbol myristate acetate.蛋白磷酸酶2A增强佛波酯对1型人类免疫缺陷病毒的激活作用。
J Virol. 2003 Feb;77(3):2276-81. doi: 10.1128/jvi.77.3.2276-2281.2003.