NanoTherapeutics Research Laboratory, Department of Chemistry, and.
NanoTherapeutics Research Laboratory, Department of Chemistry, andDepartment of Physiology and Pharmacology, University of Georgia, Athens, GA 30602
Proc Natl Acad Sci U S A. 2014 Jul 22;111(29):10444-9. doi: 10.1073/pnas.1405244111. Epub 2014 Jul 7.
Chemoresistance of cisplatin therapy is related to extensive repair of cisplatin-modified DNA in the nucleus by the nucleotide excision repair (NER). Delivering cisplatin to the mitochondria to attack mitochondrial genome lacking NER machinery can lead to a rationally designed therapy for metastatic, chemoresistant cancers and might overcome the problems associated with conventional cisplatin treatment. An engineered hydrophobic mitochondria-targeted cisplatin prodrug, Platin-M, was constructed using a strain-promoted alkyne-azide cycloaddition chemistry. Efficient delivery of Platin-M using a biocompatible polymeric nanoparticle (NP) based on biodegradable poly(lactic-co-glycolic acid)-block-polyethyleneglycol functionalized with a terminal triphenylphosphonium cation, which has remarkable activity to target mitochondria of cells, resulted in controlled release of cisplatin from Platin-M locally inside the mitochondrial matrix to attack mtDNA and exhibited otherwise-resistant advanced cancer sensitive to cisplatin-based chemotherapy. Identification of an optimized targeted-NP formulation with brain-penetrating properties allowed for delivery of Platin-M inside the mitochondria of neuroblastoma cells resulting in ∼17 times more activity than cisplatin. The remarkable activity of Platin-M and its targeted-NP in cisplatin-resistant cells was correlated with the hyperpolarization of mitochondria in these cells and mitochondrial bioenergetics studies in the resistance cells further supported this hypothesis. This unique dual-targeting approach to controlled mitochondrial delivery of cisplatin in the form of a prodrug to attack the mitochondrial genome lacking NER machinery and in vivo distribution of the delivery vehicle in the brain suggested previously undescribed routes for cisplatin-based therapy.
顺铂治疗的耐药性与核内核苷酸切除修复 (NER) 对顺铂修饰的 DNA 的广泛修复有关。将顺铂递送到缺乏 NER 机制的线粒体以攻击线粒体基因组,可能会导致针对转移性、耐药性癌症的合理设计的治疗方法,并可能克服与传统顺铂治疗相关的问题。使用应变促进的炔烃-叠氮化物环加成化学构建了一种工程化的疏水性靶向线粒体的顺铂前药 Platin-M。使用基于可生物降解的聚(乳酸-共-乙醇酸)-嵌段-聚乙二醇的生物相容性聚合物纳米颗粒 (NP) 高效递送 Platin-M,该 NP 用末端三苯基膦阳离子功能化,具有显著靶向细胞线粒体的活性,导致顺铂从 Platin-M 在内质网基质中局部释放,从而攻击 mtDNA,并使原本对顺铂化疗耐药的晚期癌症变得敏感。具有脑穿透特性的优化靶向-NP 制剂的鉴定允许 Platin-M 递送到神经母细胞瘤细胞的线粒体中,其活性比顺铂高约 17 倍。Platin-M 和其靶向-NP 在耐药细胞中的显著活性与这些细胞中线粒体的超极化以及耐药细胞中的线粒体生物能研究相关,进一步支持了这一假设。这种独特的双重靶向方法将顺铂前药以控制的方式递送到线粒体中,以攻击缺乏 NER 机制的线粒体基因组,并在体内将递药载体递送到大脑中,提示了以前未描述的顺铂治疗途径。