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New cytotoxic drugs and targets in oncology.

作者信息

Beijnen J H

机构信息

Hospital/Netherlands Cancer Institute, Amsterdam.

出版信息

Pharm Weekbl Sci. 1992 Aug 21;14(4A):258-67. doi: 10.1007/BF01962548.

DOI:10.1007/BF01962548
PMID:1437508
Abstract

New agents in the preclinical and early clinical pipeline (phases I and II) are described and some of the problems associated with their development are reviewed. The article focuses on tubulin poisons such as taxol, topoisomerase inhibitors, such as topotecan, and drugs such as bryostatin 1 and miltefosin, which interfere with specific signal transduction pathways involved in malignant cell growth.

摘要

相似文献

1
New cytotoxic drugs and targets in oncology.
Pharm Weekbl Sci. 1992 Aug 21;14(4A):258-67. doi: 10.1007/BF01962548.
2
DNA sequence selectivity of topoisomerases and topoisomerase poisons.拓扑异构酶和拓扑异构酶毒物的DNA序列选择性
Biochim Biophys Acta. 1998 Oct 1;1400(1-3):185-94. doi: 10.1016/s0167-4781(98)00135-3.
3
Synergistic interaction between topotecan and microtubule-interfering agents.
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4
Topoisomerase I-mediated DNA cleavage as a guide to the development of antitumor agents derived from the marine alkaloid lamellarin D: triester derivatives incorporating amino acid residues.拓扑异构酶I介导的DNA切割作为开发源自海洋生物碱片螺素D的抗肿瘤药物的指南:掺入氨基酸残基的三酯衍生物。
Bioorg Med Chem. 2004 Apr 1;12(7):1697-712. doi: 10.1016/j.bmc.2004.01.020.
5
Topoisomerase-targeting antitumor drugs.
Biochim Biophys Acta. 1989 Dec 17;989(2):163-77. doi: 10.1016/0304-419x(89)90041-3.
6
[Poisons of DNA topoisomerases I and II].[DNA拓扑异构酶I和II的毒物]
Bull Cancer. 1993 Nov;80(11):923-54.
7
Chinese hamster ovary cells resistant to the topoisomerase II catalytic inhibitor ICRF-159: a Tyr49Phe mutation confers high-level resistance to bisdioxopiperazines.对拓扑异构酶II催化抑制剂ICRF-159具有抗性的中国仓鼠卵巢细胞:Tyr49Phe突变赋予对双二氧哌嗪的高水平抗性。
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8
Recent advances in the development of dual topoisomerase I and II inhibitors as anticancer drugs.近年来,双重拓扑异构酶 I 和 II 抑制剂作为抗癌药物的发展取得了进展。
Curr Med Chem. 2010;17(35):4270-90. doi: 10.2174/092986710793361252.
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Catalytic inhibitors of DNA topoisomerase II.
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Discovery and Development of Topoisomerase Inhibitors as Anticancer Agents.作为抗癌药物的拓扑异构酶抑制剂的发现与开发。
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引用本文的文献

1
Pharmaceutical development of a parenteral formulation of the novel anti-tumor agent carzelesin (U-80,244).新型抗肿瘤药物卡泽雷辛(U-80,244)注射用制剂的药学研发
Invest New Drugs. 1994;12(4):303-14. doi: 10.1007/BF00873045.

本文引用的文献

1
Taxol: an antimitotic agent with a new mechanism of action.紫杉醇:一种具有全新作用机制的抗有丝分裂剂。
Pharmacol Ther. 1984;25(1):83-125. doi: 10.1016/0163-7258(84)90025-1.
2
Taxol induces the assembly of free microtubules in living cells and blocks the organizing capacity of the centrosomes and kinetochores.紫杉醇可诱导活细胞中游离微管的组装,并阻断中心体和动粒的组织能力。
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5608-612. doi: 10.1073/pnas.78.9.5608.
3
Plant antitumor agents. VI. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia.
植物抗肿瘤剂。VI. 紫杉醇的分离与结构,一种从短叶红豆杉中提取的新型抗白血病和抗肿瘤剂。
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Antineoplastic components of marine animals.海洋动物的抗肿瘤成分。
Nature. 1970 Aug 29;227(5261):962-3. doi: 10.1038/227962a0.
5
Toxicity of camptothecin (NSC-100880).喜树碱(NSC - 100880)的毒性
Cancer Chemother Rep 3. 1974 Sep;5(1):25-36.
6
Didemnin B. The first marine compound entering clinical trials as an antineoplastic agent.地棘蛙素B。第一种作为抗肿瘤药物进入临床试验的海洋化合物。
Invest New Drugs. 1986;4(3):279-84. doi: 10.1007/BF00179597.
7
Overproduction of protein kinase C causes disordered growth control in rat fibroblasts.蛋白激酶C的过度产生会导致大鼠成纤维细胞生长控制紊乱。
Cell. 1988 Feb 12;52(3):343-54. doi: 10.1016/s0092-8674(88)80027-8.
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Clinical phase I pilot study of the alkyl lysophospholipid derivative ET-18-OCH3.
Lipids. 1987 Nov;22(11):967-9. doi: 10.1007/BF02535566.
9
Protein kinase C as the receptor for the phorbol ester tumor promoters: sixth Rhoads memorial award lecture.蛋白激酶C作为佛波酯肿瘤启动子的受体:第六届罗兹纪念奖讲座
Cancer Res. 1988 Jan 1;48(1):1-8.
10
Altered growth regulation and enhanced tumorigenicity of NIH 3T3 fibroblasts transfected with protein kinase C-I cDNA.用蛋白激酶C-I cDNA转染的NIH 3T3成纤维细胞的生长调节改变及致瘤性增强。
Cell. 1988 Feb 12;52(3):447-58. doi: 10.1016/s0092-8674(88)80037-0.