Department of Chemistry and Institute for Drug Discovery, Purdue University , West Lafayette, Indiana 47907, United States.
Mol Pharm. 2017 Nov 6;14(11):3859-3865. doi: 10.1021/acs.molpharmaceut.7b00583. Epub 2017 Oct 17.
The neurokinin-1 receptor (NK1R) plays a significant role in the progression and metastasis of several neuroendocrine tumors. Due to its upregulation in these cancers, NK1R constitutes an attractive receptor for development of ligand-targeted imaging and therapeutic agents. In this report, we present the design and synthesis of an NK1R targeting ligand conjugated to the chemotherapeutic agent, tubulysin B hydrazide (TubBH), via a self-immolative linker. We then explore the ability of this low molecular weight tubulysin conjugate to kill NK1R overexpressing cancer cells both in vitro and in vivo without killing receptor negative healthy cells. Because similar studies in mice bearing NK1-negative tumors reveal no therapeutic impact, we conclude that our NK1R targeting ligand is specific for NK1R-expressing cells. Taken together, the data suggest a possible new approach for the treatment of NK1R-positive neuroendocrine cancers.
神经激肽-1 受体(NK1R)在几种神经内分泌肿瘤的进展和转移中起着重要作用。由于其在这些癌症中的上调,NK1R 成为开发配体靶向成像和治疗剂的有吸引力的受体。在本报告中,我们设计并合成了一种通过自毁性连接子与化疗药物tubulysin B 酰肼(TubBH)偶联的 NK1R 靶向配体。然后,我们研究了这种低分子量 tubulysin 缀合物在体外和体内杀死 NK1R 过表达癌细胞的能力,而不会杀死受体阴性的健康细胞。由于在携带 NK1 阴性肿瘤的小鼠中进行的类似研究没有显示出治疗效果,我们得出结论,我们的 NK1R 靶向配体是 NK1R 表达细胞的特异性配体。综上所述,这些数据为治疗 NK1R 阳性神经内分泌癌提供了一种新的可能方法。