Suppr超能文献

通过米托蒽醌的胶束递送使癌细胞对TRAIL诱导的死亡敏感化。

Sensitizing cancer cells to TRAIL-induced death by micellar delivery of mitoxantrone.

作者信息

Grandhi Taraka Sai Pavan, Potta Thrimoorthy, Taylor David J, Tian Yanqing, Johnson Roger H, Meldrum Deirdre R, Rege Kaushal

机构信息

Harrington Biomedical Engineering, Arizona State University, Tempe, AZ 85287, USA.

出版信息

Nanomedicine (Lond). 2014;9(12):1775-88. doi: 10.2217/nnm.13.125. Epub 2013 Nov 6.

Abstract

TNFα-related apoptosis-inducing ligand (TRAIL) induces death selectively in cancer cells. However, subpopulations of cancer cells are either resistant to or can develop resistance to TRAIL-induced death. As a result, strategies that overcome this resistance are currently under investigation. We have recently identified several US FDA-approved drugs with TRAIL-sensitization activity against prostate, breast and pancreatic cancer cells. Mitoxantrone, a previously unknown TRAIL sensitizer identified in the screen, was successfully encapsulated in methoxy-, amine- and carboxyl-terminated PEG-DSPE micelles in order to facilitate delivery of the drug to cancer cells. All three micelle types were extensively characterized for their physicochemical properties and evaluated for their ability to sensitize cancer cells to TRAIL-induced death. Our results indicate that micelle-encapsulated mitoxantrone can be advantageously employed in synergistic treatments with TRAIL, leading to a biocompatible delivery system and amplified cell killing activity for combination chemotherapeutic cancer treatments.

摘要

肿瘤坏死因子α相关凋亡诱导配体(TRAIL)可选择性地诱导癌细胞死亡。然而,癌细胞亚群对TRAIL诱导的死亡具有抗性或可产生抗性。因此,目前正在研究克服这种抗性的策略。我们最近鉴定出几种美国食品药品监督管理局(FDA)批准的对前列腺癌、乳腺癌和胰腺癌细胞具有TRAIL增敏活性的药物。米托蒽醌是在筛选中发现的一种此前未知的TRAIL增敏剂,已成功包裹于甲氧基、氨基和羧基末端的聚乙二醇-二硬脂酰磷脂酰乙醇胺(PEG-DSPE)胶束中,以便于将药物递送至癌细胞。对所有三种胶束类型的物理化学性质进行了广泛表征,并评估了它们使癌细胞对TRAIL诱导的死亡增敏的能力。我们的结果表明,胶束包裹的米托蒽醌可有利地用于与TRAIL的联合治疗,从而形成一种生物相容性递送系统,并增强联合化疗癌症治疗的细胞杀伤活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验