摘要
背景:微管蛋白是肿瘤治疗的重要靶点,这归因于其靶向MT动力学和干扰关键细胞功能的能力,包括有丝分裂、细胞信号传导和细胞内运输。几种微管蛋白抑制剂已被批准用于临床应用。但其耐药、毒副作用等缺点限制了其临床应用。与单靶点药物相比,多靶点药物可以有效提高疗效,减少副作用,克服耐药性的发展。微管蛋白降解剂不需要高浓度,可以回收利用。降解后,蛋白质需要重新合成以恢复功能,这大大延缓了耐药性的发展。 方法:使用SciFinder®作为工具,对基于微管蛋白的双靶点抑制剂和微管蛋白降解剂的出版物进行调查,排除已发表的专利。 结果:本研究介绍了基于微管蛋白的双靶点抑制剂和微管蛋白降解剂作为抗肿瘤药物的研究进展,为开发和应用更有效的癌症治疗药物提供参考。 结论:多靶点抑制剂和蛋白质降解剂在肿瘤治疗中具有克服多药耐药和减少副作用的发展前景。目前,微管蛋白双靶点抑制剂的设计还有待进一步优化,蛋白质降解的详细机制值得进一步明确。
关键词: 微管蛋白抑制剂,基于微管蛋白的双靶点抑制剂,蛋白质降解剂,多药耐药,副作用,癌症治疗。
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