| Literature DB >> 32266902 |
Miao-Deng Liu1, Yun Yu, Deng-Ke Guo, Shi-Bo Wang, Chu-Xin Li, Fan Gao, Cheng Zhang, Bo-Ru Xie, Zhenlin Zhong, Xian-Zheng Zhang.
Abstract
Selectively attenuating the protection offered by heat shock protein 90 (HSP90), which is indispensable for the stabilization of the essential regulators of cell survival and works as a cell guardian under oxidative stress conditions, is a potential approach to improve the efficiency of cancer therapy. Here, we designed a biodegradable nanoplatform (APCN/BP-FA) based on a Zr(iv)-based porphyrinic porous coordination network (PCN) and black phosphorus (BP) sheets for efficient photodynamic therapy (PDT) by enhancing the accumulation of the nanoplatforms in the tumor area and attenuating the protection of cancer cells. Owing to the favorable degradability of BP, the nanosystem exhibited accelerated the release of the HSP90 inhibitor tanespimycin (17-AAG) and an apparent promotion in the reactive oxygen species (ROS) yield of PCN as well as expedited the degradation of the PCN-laden BP nanoplatforms. Both in vitro and in vivo results revealed that the elevated amounts of ROS and reduced cytoprotection in tumor cells were caused by the nanoplatforms. This strategy may provide a promising method for attenuating cytoprotection to aid efficient photodynamic therapy.Entities:
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Year: 2020 PMID: 32266902 DOI: 10.1039/d0nr00956c
Source DB: PubMed Journal: Nanoscale ISSN: 2040-3364 Impact factor: 7.790