| Literature DB >> 28686804 |
Yongbo Peng1, Zilong Zhao1, Teng Liu1,2, Xiong Li2, Xiaoxiao Hu1, Xiaoping Wei3, Xiaobing Zhang1, Weihong Tan1,4.
Abstract
Arsenic trioxide (ATO, As2 O3 ) is currently used to treat acute promyelocytic leukemia. However, expanding its use to include high-dose treatment of other cancers is severely hampered by serious side effects on healthy organs. To address these limitations, we loaded ATO onto folate (FA)-labeled human serum albumin (HSA) pretreated with glutathione (GSH) based on the low pH- and GSH-sensitive arsenic-sulfur bond, and we termed the resulting smart nanodrug as FA-HSA-ATO. FA-HSA-ATO could specifically recognize folate receptor-β-positive (FRβ+) chronic myeloid leukemia (CML) cells, resulting in more intracellular accumulation of ATO. Furthermore, the nanodrug could upregulate FRβ expression in CML cancer cells and xenograft tumor model, facilitating even more recruitment and uptake of FRβ-targeting drugs. In vitro and in vivo experiments indicate that the nanodrug significantly alleviates side effects and improves therapeutic efficacy of ATO on CML and xenograft tumor model.Entities:
Keywords: arsenic trioxide; chronic myeloid leukemia; folate receptor-β; human serum albumin; smart nanodrugs
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Year: 2017 PMID: 28686804 PMCID: PMC5912668 DOI: 10.1002/anie.201701366
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336