摘要
分子靶向抗癌疗法涵盖了在一种指定肿瘤的发生、发展、扩散(全过程)中作用于特殊分子靶点的药物或其它物质的使用方法。相比之下,大部分传统化学疗法作用于所有快速增殖的细胞,而不论是健康细胞还是癌细胞。靶向抗癌药物被设计为满足特定需求并具有传统化学药物细胞稳定性和无细胞毒性的药物。目前,人们发现了300多个的生物分子靶点。(其中,)关于细胞代谢的蛋白质有受体蛋白、信号传导蛋白、参与致瘤性转变的mRNA线基质合成蛋白、细胞周期控制蛋白、功能蛋白和结构蛋白。 目前,包括上皮生长因子受体(EGFR, epithelial growth factor receptor)、血小板源性生长因子受体(PDGFR, platelet-derived growth factor receptor)、血管内皮生长因子受体(VEGFR, vascular endothelial growth factor receptor)在内的抗癌药物是以受体蛋白为靶点。靶向抗癌药物可能影响细胞外受体域(抗体)或细胞间受体域(酪氨酸激酶抑制剂)。 阻碍含癌基因结构信息的线性mRNA(信号传导蛋白)是抗癌药物的另一分子靶点。这种在进行临床试验的治疗方法,被称为反义疗法。 当遗传物质的合成被扰乱时,大多数情况下进入下一周期相的通道会关闭。负责关闭的关键蛋白是cyclines和cycline- 依赖性酶(CDK)。临床试验着重于研究关闭不同CDK的天然与合成物质。 这篇文章讨论了分子靶点、已批准的靶向抗癌药物化学结构和最近被用于抗癌疗法药物的应用说明与其禁忌症候。
关键词: 单克隆抗体,酪氨酸抑制酶,mTOR途径,化学结构,作用机制,副作用,药物代谢动力学参数
Current Medicinal Chemistry
Title:New Molecular Targets of Anticancer Therapy – Current Status and Perspectives
Volume: 23 Issue: 37
Author(s): Marianna Zajac, Izabela Muszalska, Anna Jelinska
Affiliation:
关键词: 单克隆抗体,酪氨酸抑制酶,mTOR途径,化学结构,作用机制,副作用,药物代谢动力学参数
摘要: Molecularly targeted anticancer therapy involves the use of drugs or other substances affecting specific molecular targets that play a part in the development, progression and spread of a given neoplasm. By contrast, the majority of classical chemotherapeutics act on all rapidly proliferating cells, both healthy and cancerous ones. Target anticancer drugs are designed to achieve a particular aim and they usually act cytostatically, not cytotoxically like classical chemotherapeutics. At present, more than 300 biological molecular targets have been identified. The proteins involved in cellular metabolism include (among others) receptor proteins, signal transduction proteins, mRNA thread matrix synthesis proteins participating in neoplastic transformation, cell cycle control proteins, functional and structural proteins.
The receptor proteins that are targeted by currently used anticancer drugs comprise the epithelial growth factor receptor (EGFR), platelet-derived growth factor receptor (PDGFR) and vascular endothelial growth factor receptor(VEGFR). Target anticancer drugs may affect extracellular receptor domains (antibodies) or intracellular receptor domains (tyrosine kinase inhibitors).
The blocking of the mRNA thread containing information about the structure of oncogenes (signal transduction proteins) is another molecular target of anticancer drugs. That type of treatment, referred to as antisense therapy, is in clinical trials.
When the synthesis of genetic material is disturbed, in most cases the passage to the next cycle phase is blocked. The key proteins responsible for the blockage are cyclines and cycline- dependent kinases (CDK). Clinical trials are focused on natural and synthetic substances capable of blocking various CDKs.
The paper discusses the molecular targets and chemical structure of target anticancer drugs that have been approved for and currently applied in antineoplastic therapy together with indications and contraindications for their application.
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Cite this article as:
Marianna Zajac, Izabela Muszalska, Anna Jelinska , New Molecular Targets of Anticancer Therapy – Current Status and Perspectives, Current Medicinal Chemistry 2016; 23 (37) . https://dx.doi.org/10.2174/0929867323666160814002150
DOI https://dx.doi.org/10.2174/0929867323666160814002150 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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