Emerging role of necroptosis, pyroptosis, and ferroptosis in breast cancer: New dawn for overcoming therapy resistance

被引:5
|
作者
Fu, Bifei [1 ]
Lou, Yuming [1 ]
Wu, Pu [2 ]
Lu, Xiaofeng [1 ]
Xu, Chaoyang [1 ,2 ]
机构
[1] Zhejiang Univ, Affiliated Jinhua Hosp, Sch Med, Dept Breast & Thyroid Surg, Jinhua 321000, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Jinhua Hosp, Sch Med, Cent Lab, Jinhua 321000, Zhejiang, Peoples R China
来源
NEOPLASIA | 2024年 / 55卷
关键词
Breast cancer; Necroptosis; Pyroptosis; Ferroptosis; Drug resistance; MOLECULAR-MECHANISMS; PROGRAMMED NECROSIS; TUMOR NECROSIS; CELL-DEATH; RIP3; INFLAMMASOME; METHYLATION; INDUCTION; APOPTOSIS; SHIKONIN;
D O I
10.1016/j.neo.2024.101017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer (BC) is one of the primary causes of death in women worldwide. The challenges associated with adverse outcomes have increased significantly, and the identification of novel therapeutic targets has become increasingly urgent. Regulated cell death (RCD) refers to a type of cell death that can be regulated by several different biomacromolecules, which is distinctive from accidental cell death (ACD). In recent years, apoptosis, a representative RCD pathway, has gained significance as a target for BC medications. However, tumor cells exhibit avoidance of apoptosis and result in treatment resistance, which emphasizes further studies devoted to alternative cell death processes, namely necroptosis, pyroptosis, and ferroptosis. Here, in this review, we focus on summarizing the crucial signaling pathways of these RCD in BC. We further discuss the molecular mechanism and potentiality in clinical application of several prospective drugs, nanoparticles, and other small compounds targeting different RCD subroutines of BC. We also discuss the benefits of modulating RCD processes on drug resistance and the advantages of combining RCD modulators with conventional treatments in BC. This review will deepen our understanding of the relationship between RCD and BC, and shed new light on future directions to attack cancer vulnerabilities with RCD modulators for therapeutic purposes.
引用
收藏
页数:11
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