Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37212, USA.
Molecules. 2020 Dec 31;26(1):157. doi: 10.3390/molecules26010157.
Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) induces cancer cell-specific apoptosis and has garnered intense interest as a promising agent for cancer treatment. However, the development of TRAIL has been hampered in part because most human cancer cells are resistant to TRAIL. A few small molecules including natural compounds such as piperlongumine (PL) have been reported to sensitize cancer cells to TRAIL. We prepared a novel type of nanomaterial, micelle-in-liposomes (MILs) for solubilization and delivery of PL. PL-loaded MILs were used to sensitize cancer cells to TRAIL. As visualized by cryo-TEM, micelles were successfully loaded inside the aqueous core of liposomes. The MILs increased the water solubility of PL by ~20 fold. A sustained PL release from MILs in physiologically relevant buffer over 7 days was achieved, indicating that the liposomes prevented premature drug release from the micelles in the MILs. Also demonstrated is a potent synergistic apoptotic effect in cancer cells by PL MILs in conjunction with liposomal TRAIL. MILs provide a new formulation and delivery vehicle for hydrophobic anticancer agents, which can be used alone or in combination with TRAIL to promote cancer cell death.
肿瘤坏死因子(TNF)相关凋亡诱导配体(TRAIL)诱导癌细胞特异性凋亡,并作为一种有前途的癌症治疗药物引起了广泛关注。然而,TRAIL 的发展受到了部分阻碍,因为大多数人类癌细胞对 TRAIL 具有抗性。一些小分子,包括天然化合物如胡椒碱(PL),已被报道能使癌细胞对 TRAIL 敏感。我们制备了一种新型纳米材料,胶束包载脂质体(MILs)用于 PL 的溶解和递送。负载 PL 的 MILs 用于使癌细胞对 TRAIL 敏感。如冷冻透射电镜所示,胶束成功地装载在脂质体的水核内。MILs 将 PL 的水溶性提高了约 20 倍。在生理相关的缓冲液中,MILs 中 PL 能够持续释放 7 天,表明脂质体防止了 MILs 中胶束内药物的过早释放。还证明了 PL-MILs 与脂质体 TRAIL 联合使用可在癌细胞中产生强烈的协同凋亡效应。MILs 为疏水性抗癌药物提供了一种新的制剂和递送载体,可单独使用或与 TRAIL 联合使用以促进癌细胞死亡。