Literature DB >> 26888039

Nano-Fenton Reactors as a New Class of Oxidative Stress Amplifying Anticancer Therapeutic Agents.

Byeongsu Kwon1, Eunji Han1, Wonseok Yang1, Wooram Cho1, Wooyoung Yoo1, Junyeon Hwang2, Byoung-Mog Kwon3, Dongwon Lee1,4.   

Abstract

Cancer cells, compared to normal cells, are under oxidative stress associated with an elevated level of reactive oxygen species (ROS) and are more vulnerable to oxidative stress induced by ROS generating agents. Thus, manipulation of the ROS level provides a logical approach to kill cancer cells preferentially, without significant toxicity to normal cells, and great efforts have been dedicated to the development of strategies to induce cytotoxic oxidative stress for cancer treatment. Fenton reaction is an important biological reaction in which irons convert hydrogen peroxide (H2O2) to highly toxic hydroxyl radicals that escalate ROS stress. Here, we report Fenton reaction-performing polymer (PolyCAFe) micelles as a new class of ROS-manipulating anticancer therapeutic agents. Amphiphilic PolyCAFe incorporates H2O2-generating benzoyloxycinnamaldehyde and iron-containing compounds in its backbone and self-assembles to form micelles that serve as Nano-Fenton reactors to generate cytotoxic hydroxyl radicals, killing cancer cells preferentially. When intravenously injected, PolyCAFe micelles could accumulate in tumors preferentially to remarkably suppress tumor growth, without toxicity to normal tissues. This study demonstrates the tremendous translatable potential of Nano-Fenton reactors as a new class of anticancer drugs.

Entities:  

Keywords:  Fenton reaction; cancer; hydroxyl radical; oxidative stress; polymeric micelles

Mesh:

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Year:  2016        PMID: 26888039     DOI: 10.1021/acsami.5b12523

Source DB:  PubMed          Journal:  ACS Appl Mater Interfaces        ISSN: 1944-8244            Impact factor:   9.229


  5 in total

1.  Dual-emission copper nanoclusters-based ratiometric fluorescent probe for intracellular detection of hydroxyl and superoxide anion species.

Authors:  Shlok Jindal; Shefali Garg; Ishita Matai; Gopinath Packirisamy; Abhay Sachdev
Journal:  Mikrochim Acta       Date:  2021-01-03       Impact factor: 5.833

2.  Acid-responsive nanoparticles as a novel oxidative stress-inducing anticancer therapeutic agent for colon cancer.

Authors:  Chengwei Zhao; Weilan Cao; Hailun Zheng; Zhongxiang Xiao; Jie Hu; Lehe Yang; Min Chen; Guang Liang; Suqing Zheng; Chengguang Zhao
Journal:  Int J Nanomedicine       Date:  2019-02-28

3.  Co-Administration of iRGD with Sorafenib-Loaded Iron-Based Metal-Organic Framework as a Targeted Ferroptosis Agent for Liver Cancer Therapy.

Authors:  Xianchuang Liu; Xinyang Zhu; Xun Qi; Xianwei Meng; Ke Xu
Journal:  Int J Nanomedicine       Date:  2021-02-11

4.  Ellagic acid-Fe@BSA nanoparticles for endogenous H2S accelerated Fe(III)/Fe(II) conversion and photothermal synergistically enhanced chemodynamic therapy.

Authors:  Qingqing Tian; Lu An; Qiwei Tian; Jiaomin Lin; Shiping Yang
Journal:  Theranostics       Date:  2020-03-04       Impact factor: 11.556

5.  Broaden sources and reduce expenditure: Tumor-specific transformable oxidative stress nanoamplifier enabling economized photodynamic therapy for reinforced oxidation therapy.

Authors:  Xiaoyu Xu; Binyao Huang; Zishan Zeng; Jie Chen; Zeqian Huang; Zilin Guan; Meixu Chen; Yanjuan Huang; Chunshun Zhao
Journal:  Theranostics       Date:  2020-08-21       Impact factor: 11.556

  5 in total

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