Ferroptosis-based nano delivery systems targeted therapy for colorectal cancer: Insights and future perspectives

被引:30
|
作者
Qiao, Chu [1 ]
Wang, Haiying [1 ]
Guan, Qiutong [1 ]
Wei, Minjie [1 ]
Li, Zhenhua [1 ]
机构
[1] China Med Univ, Sch Pharm, Shenyang 110122, Peoples R China
关键词
Colorectal cancer; Ferroptosis; Iron metabolism; Lipid metabolism; Nano delivery system; Immunotherapy; FERRITIN NANOPARTICLES; TUMOR MICROENVIRONMENT; PHOTODYNAMIC THERAPY; STEM-CELLS; DOXORUBICIN; IRON; ACTIVATION; SORAFENIB;
D O I
10.1016/j.ajps.2022.09.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
There are limited options for patients who develop liver metastasis from colorectal cancer (CRC), the leading cause of cancer-related mortality worldwide. Emerging evidence has provided insights into iron deficiency and excess in CRC. Ferroptosis is an iron-dependent form of programmed cell death characterized by aberrant iron and lipid metabolism, which play crucial roles in tumorigenesis, tumor progression, and treatment options. A better understanding of the underlying molecular mechanism of ferroptosis has shed light on the current findings of ferroptosis-based nanodrug targeting strategies, such as driving ferroptosis in tumor cells and the tumor microenvironment, emerging combination therapy and against multidrug resistance. Furthermore, this review highlights the challenge and perspective of a ferroptosis-driven nanodrug delivery system for CRC-targeted therapy.(c) 2022 Shenyang Pharmaceutical University. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
收藏
页码:613 / 629
页数:17
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