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砷剂纳米药物用于实体瘤治疗的现状与展望。

Current status and future prospects of nanomedicine for arsenic trioxide delivery to solid tumors.

机构信息

Department of Pediatric Hematology and Oncology, University Children's Hospital Muenster, Muenster, Germany.

Chair of Solid State and Materials Chemistry, Institute of Physics, University of Augsburg, Augsburg, Germany.

出版信息

Med Res Rev. 2022 Jan;42(1):374-398. doi: 10.1002/med.21844. Epub 2021 Jul 26.


DOI:10.1002/med.21844
PMID:34309879
Abstract

Despite having a rich history as a poison, arsenic and its compounds have also gained a great reputation as promising anticancer drugs. As a pioneer, arsenic trioxide has been approved for the treatment of acute promyelocytic leukemia. Many in vitro studies suggested that arsenic trioxide could also be used in the treatment of solid tumors. However, the transition from bench to bedside turned out to be challenging, especially in terms of the drug bioavailability and concentration reaching tumor tissues. To address these issues, nanomedicine tools have been proposed. As nanocarriers of arsenic trioxide, various materials have been examined including liposomes, polymer, and inorganic nanoparticles, and many other materials. This review gives an overview of the existing strategies of delivery of arsenic trioxide in cancer treatment with a focus on the drug encapsulation approaches and medicinal impact in the treatment of solid tumors. It focuses on the progress in the last years and gives an outlook and suggestions for further improvements including theragnostic approaches and targeted delivery.

摘要

尽管砷及其化合物作为一种毒药具有悠久的历史,但它们也因其有望成为抗癌药物而获得了很高的声誉。作为先驱者,三氧化二砷已被批准用于治疗急性早幼粒细胞白血病。许多体外研究表明,三氧化二砷也可用于治疗实体瘤。然而,从实验室到临床的转变结果颇具挑战性,特别是在药物生物利用度和到达肿瘤组织的浓度方面。为了解决这些问题,已经提出了纳米医学工具。作为三氧化二砷的纳米载体,已经研究了各种材料,包括脂质体、聚合物和无机纳米粒子以及许多其他材料。本综述概述了在癌症治疗中三氧化二砷传递的现有策略,重点介绍了药物包封方法和在治疗实体瘤方面的医学影响。它侧重于近年来的进展,并对进一步改进提出了展望和建议,包括诊断治疗方法和靶向传递。

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Current status and future prospects of nanomedicine for arsenic trioxide delivery to solid tumors.

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[2]
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In situ valence-transited arsenic nanosheets for multi-modal therapy of colorectal cancer.

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[2]
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[3]
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Mol Med. 2024-12-19

[4]
Carboplatin combined with arsenic trioxide versus carboplatin combined with docetaxel treatment for LACC: A randomized, open-label, phase II clinical study.

Open Med (Wars). 2024-12-12

[5]
Arsenic Nanoparticles Trigger Apoptosis via Induction in OECM-1 Cells.

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[6]
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[7]
Research progress on arsenic, arsenic-containing medicinal materials, and arsenic-containing preparations: clinical application, pharmacological effects, and toxicity.

Front Pharmacol. 2024-3-1

[8]
Arsenic trioxide-induced cardiotoxicity: the protective effect of 2-aminoethoxydiphenyl-borate.

Acta Biochim Biophys Sin (Shanghai). 2024-4-25

[9]
Reduced Proteolipid Protein 2 promotes endoplasmic reticulum stress-related apoptosis and increases drug sensitivity in acute myeloid leukemia.

Mol Biol Rep. 2023-12-12

[10]
The genomic landscape of sensitivity to arsenic trioxide uncovered by genome-wide CRISPR-Cas9 screening.

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