Ferroptosis of immune cells in the tumor microenvironment

被引:43
|
作者
Kim, Rina [1 ]
Taylor, Devon [2 ]
Vonderheide, Robert H. [1 ,3 ,4 ,5 ]
Gabrilovich, Dmitry I. [2 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Med, Philadelphia, PA USA
[2] AstraZeneca, R&D Oncol, Gaithersburg, MD 20878 USA
[3] Univ Penn, Abramson Canc Ctr, Philadelphia, PA USA
[4] Univ Penn, Inst Immunol, Perelman Sch Med, Philadelphia, PA USA
[5] Univ Penn, Parker Inst Canc Immunotherapy, Philadelphia, PA USA
关键词
LIPID-PEROXIDATION; PROMOTES FERROPTOSIS; OXIDIZED LIPIDS; DENDRITIC CELLS; REDOX BIOLOGY; CANCER; DEATH; MACROPHAGES; MECHANISMS; GENERATION;
D O I
10.1016/j.tips.2023.06.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ferroptosis is a distinct form of cell death driven by the accumulation of peroxidized lipids. Characterized by alterations in redox lipid metabolism, ferrop-tosis has been implicated in a variety of cellular processes, including cancer. In-duction of ferroptosis is considered a novel way to kill tumor cells, especially cells resistant to radiation and chemotherapy. However, in recent years, a new paradigm has emerged. In addition to promoting tumor cell death, ferroptosis causes potent immune suppression in the tumor microenvironment (TME) by af-fecting both innate and adaptive immune responses. In this review, we discuss the dual role of ferroptosis in the antitumor and protumorigenic functions of im-mune cells in cancer. We suggest strategies for targeting ferroptosis, taking into account its ambiguous role in cancer.
引用
收藏
页码:542 / 552
页数:11
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