Mitochondria-Targeted Prodrug Nanoassemblies for Efficient Ferroptosis-Based Therapy via Devastating Ferroptosis Defense Systems-Reference-Cited by-同舟云学术

Mitochondria-Targeted Prodrug Nanoassemblies for Efficient Ferroptosis-Based Therapy via Devastating Ferroptosis Defense Systems

Published:2024-03-07 Issue:11 Volume:18 Page:7945-7958
ISSN:1936-0851
Container-title:ACS Nano
language:en
Short-container-title:ACS Nano

Author:

Liu Nian¹,Lin Qian¹,Huang Zhenkun¹,Liu Chen¹,Qin Jingbo²,Yu Yanlin¹,Chen Weibin³,Zhang Jingbo¹,Jiang Min¹,Gao Xuemin¹,Huo Shuaidong¹,Zhu Xuan¹

Affiliation:

1. Fujian Provincial Key Laboratory of Innovative Drug Target Research, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China

2. Guangdong Provincial Engineering Research Center of Molecular Imaging, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai 519000, China

3. School of Medicine, Xiamen University, Xiamen 361102, China

Funder

National Key Research and Development Program of China

Natural Science Foundation of Fujian Province

National Natural Science Foundation of China

Xiamen University

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acsnano.3c10133

Reference59 articles.

1. The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis

2. Renal Clearable Ultrasmall Single-Crystal Fe Nanoparticles for Highly Selective and Effective Ferroptosis Therapy and Immunotherapy

3. Broadening horizons: the role of ferroptosis in cancer

4. The molecular and metabolic landscape of iron and ferroptosis in cardiovascular disease

5. Enhanced Ferroptosis by Oxygen-Boosted Phototherapy Based on a 2-in-1 Nanoplatform of Ferrous Hemoglobin for Tumor Synergistic Therapy

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