发现新的抗癌药物。

Forum (Genoa, Italy) Pub Date : 1999-07-01
M W Lobbezoo, M R Krul, H M Pinedo
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引用次数: 0

摘要

由于最近基础研究的进展,抗癌药物的发现已经发生了根本性的变化。从历史上看,发现潜在的治疗癌症的新药在很大程度上依赖于大规模的随机筛选。虽然已经有几种有用的药物可用,但有时在开发了原始OhitO的化学类似物之后,这种方法在功效/毒性平衡方面通常令人失望。迄今为止,一系列癌症特异性分子和生物药物靶点为设计和发现特异性抗癌药物提供了机会,这些药物比传统药物具有更好的肿瘤选择性,因此毒性更小。目前在临床前和临床研究和开发项目中探索的许多创新方法包括抑制血管生成和转移,肿瘤疫苗/免疫治疗和基因治疗方法。目前在这些领域正在进行几个有希望的药物开发项目。创新抗癌药物的出现也对新药开发的组织产生了重要影响。传统的药物开发方法往往不适合具有全新作用方式的药物。因此,为这些药物设计新药开发模板在抗癌药物开发组织中具有高度的优先级。
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Discovery of new anti-cancer agents.

Anticancer drug discovery has changed fundamentally owing to recent progress in basic research. Historically, the discovery of potential new drugs for the treatment of cancer has largely relied on large-scale random screening. Although several useful agents have become available, sometimes after the development of chemical analogues of the original OhitO, this approach has generally been disappointing in terms of the efficacy/toxicity balance. To date, a range of cancer-specific molecular and biological drug targets are available providing opportunities for the design and discovery of specific anti-cancer agents with better tumour selectivity, and therefore less toxicity, than conventional agents. Among the many innovative approaches currently explored in pre-clinical and clinical research and development programs are inhibition of angiogenesis and metastasis, tumour vaccines/immunotherapy and gene therapy approaches. Several promising drug development projects are currently underway in these areas. The advent of innovative anticancer agents also has important consequences for the organisation of new drug development. Traditional drug development methodologies are often not appropriate for agents having completely new modes of action. The design of new drug development templates for such agents therefore has high priority in anti-cancer drug development organisations.

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