Department of Pharmacy and Biotechnology, University of Bologna, Via S. Donato 19/2, Bologna, Italy.
Department for Biomedical and Neuromotor Sciences (DIBINEM), University of Bologna, via Irnerio 48, Bologna, Italy.
Pharm Res. 2016 Nov;33(11):2722-35. doi: 10.1007/s11095-016-1999-9. Epub 2016 Jul 25.
We describe a novel class of antitumor amphiphilic amines (RCn) based on a tricyclic amine hydrophilic head and a hydrophobic linear alkyl tail of variable length.
We tested the lead compound, RC16, for cytotoxicity and mechanism of cell death in several cancer cell lines, anti tumor efficacy in mouse tumor models, and ability to encapsulate chemotherapy drugs.
These compounds displayed strong cytotoxic activity against cell lines derived from both pediatric and adult cancers. The IC50 of the lead compound, RC16, for normal cells including human keratinocytes, human fibroblasts and human umbilical vein endothelial cells was tenfold higher than for tumor cells. RC16 exhibited significant antitumor effects in vivo using several human xenografts and a metastatic model of murine neuroblastoma by both intravenous and oral administration routes. The amphiphilic character of RC16 triggered a spontaneous molecular self-assembling in water with formation of micelles allowing complexation of Doxorubicin, Etoposide and Paclitaxel. These micelles significantly improved the in vitro antitumor activity of these drugs as the enhancement of their aqueous solubility also improved their biologic availability.
RC16 and related amphiphilic amines may be useful as a novel cancer treatment.
我们描述了一类新型的抗肿瘤两亲性胺(RCn),它们基于三环胺亲水头部和可变长度的疏水线性烷基尾部。
我们测试了先导化合物 RC16 在几种癌细胞系中的细胞毒性和细胞死亡机制、在小鼠肿瘤模型中的抗肿瘤疗效以及包裹化疗药物的能力。
这些化合物对来源于儿科和成人癌症的细胞系表现出强烈的细胞毒性。先导化合物 RC16 对正常细胞(包括人角质形成细胞、人成纤维细胞和人脐静脉内皮细胞)的 IC50 比肿瘤细胞高十倍。RC16 通过静脉内和口服途径在几种人异种移植和小鼠神经母细胞瘤转移模型中均显示出显著的体内抗肿瘤作用。RC16 的两亲性特征在水中自发引发分子自组装,形成胶束,允许阿霉素、依托泊苷和紫杉醇的络合。这些胶束显著提高了这些药物的体外抗肿瘤活性,因为增加其水溶解度也提高了它们的生物利用度。
RC16 和相关的两亲性胺可能是一种新型癌症治疗方法的有用选择。