| Literature DB >> 27093466 |
Hiroaki Kinoh1, Yutaka Miura2, Tsukasa Chida2, Xueying Liu2, Kazue Mizuno2, Shigeto Fukushima3, Yosuke Morodomi4, Nobuhiro Nishiyama5, Horacio Cabral6, Kazunori Kataoka1,2,3,6.
Abstract
Nanomedicines capable of control over drug functions have potential for developing resilient therapies, even against tumors harboring recalcitrant cancer stem cells (CSCs). By coordinating drug interactions within the confined inner compartment of core-shell nanomedicines, we conceived multicomponent nanomedicines directed to achieve synchronized and synergistic drug cooperation within tumor cells as a strategy for enhancing efficacy, overcoming drug resistance, and eradicating CSCs. The approach was validated by using polymeric micellar nanomedicines co-incorporating the pan-kinase inhibitor staurosporine (STS), which was identified as the most potent CSC inhibitor from a panel of signaling-pathway inhibitors, and the cytotoxic agent epirubicin (Epi), through rationally contriving the affinity between the drugs. The micelles released both drugs simultaneously, triggered by acidic endosomal pH, attaining concurrent intracellular delivery, with STS working as a companion for Epi, down-regulating efflux transporters and resistance mechanisms induced by Epi. These features prompted the nanomedicines to eradicate orthotopic xenografts of Epi-resistant mesothelioma bearing a CSC subpopulation.Entities:
Keywords: cancer stem-like cells; chemotherapy; epirubicin; mesothelioma; polymeric micelles; staurosporine
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Year: 2016 PMID: 27093466 DOI: 10.1021/acsnano.6b00900
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881