植物源性蛋白酪氨酸激酶抑制剂作为抗癌剂。

Ferenc Hollósy, György Kéri
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引用次数: 33

摘要

蛋白酪氨酸激酶在调节细胞生长、分化和死亡等一系列细胞功能的信号转导途径中发挥着重要作用。因此,酪氨酸激酶是设计新的治疗药物的有吸引力的目标,不仅针对癌症,而且针对许多其他疾病。基于民族药理学和化学分类学知识,通过筛选植物提取物发现了许多酪氨酸激酶抑制剂。特定的筛选方法导致了结构上不同的抑制剂类别的分离,包括苯丙烷,查尔酮,类黄酮,香豆素,苯乙烯,醌和萜烯。这些天然抑制剂为进一步设计和合成更有活性的类似物提供了有价值的线索。许多这些抑制剂也被用于探测参与蛋白酪氨酸激酶介导的信号转导的分子和细胞机制。本文从植物源性蛋白酪氨酸激酶抑制剂及其合成类似物的植物来源、构效关系和抗癌功效等方面进行了综述。
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Plant-derived protein tyrosine kinase inhibitors as anticancer agents.

Protein tyrosine kinases play a fundamental role in signal transduction pathways regulating a number of cellular functions such as cell growth, differentiation and cell death. Tyrosine kinases are, therefore attractive targets for the design of new therapeutic agents, not only against cancer, but also against many other diseases. Numerous tyrosine kinase inhibitors have been discovered by screening of plant extracts based on ethnopharmacological and chemotaxonomical knowledge. Specific screening approaches have led to the isolation of structurally distinct classes of inhibitors, including phenylpropanes, chalcones, flavonoids, coumarins, styrenes, quinones and terpenes. These natural inhibitors have served as valuable leads for further design and synthesis of more active analogues. Many of these inhibitors have also been used in probing the molecular and cellular mechanisms involved in the protein tyrosine kinase mediated signal transduction. In this review, plant-derived protein tyrosine kinase inhibitors and their synthetic analogues were systematically evaluated based on their plant origin, structure-activity relationship and anticancer efficacy.

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