Targeting immunogenic cell death in cancer

被引:458
|
作者
Ahmed, Asma [1 ,2 ]
Tait, Stephen W. G. [1 ,2 ]
机构
[1] Canc Res UK Beatson Inst, Switchback Rd, Glasgow G61 1BD, Lanark, Scotland
[2] Univ Glasgow, Inst Canc Sci, Glasgow, Lanark, Scotland
关键词
cancer; caspase; cell death; DAMPs; immunogenic cell death; interferon; APOPTOTIC CELLS; CALRETICULIN EXPOSURE; DENDRITIC CELLS; I INTERFERONS; CHEMOTHERAPY; NECROPTOSIS; INDUCTION; IMMUNITY; DNA; INFLAMMATION;
D O I
10.1002/1878-0261.12851
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunogenic cell death (ICD) is a type of cancer cell death triggered by certain chemotherapeutic drugs, oncolytic viruses, physicochemical therapies, photodynamic therapy, and radiotherapy. It involves the activation of the immune system against cancer in immunocompetent hosts. ICD comprises the release of damage-associated molecular patterns (DAMPs) from dying tumor cells that result in the activation of tumor-specific immune responses, thus eliciting long-term efficacy of anticancer drugs by combining direct cancer cell killing and antitumor immunity. Remarkably, subcutaneous injection of dying tumor cells undergoing ICD has been shown to provoke anticancer vaccine effects in vivo. DAMPs include the cell surface exposure of calreticulin (CRT) and heat-shock proteins (HSP70 and HSP90), extracellular release of adenosine triphosphate (ATP), high-mobility group box-1 (HMGB1), type I IFNs and members of the IL-1 cytokine family. In this review, we discuss the cell death modalities connected to ICD, the DAMPs exposed during ICD, and the mechanism by which they activate the immune system. Finally, we discuss the therapeutic potential and challenges of harnessing ICD in cancer immunotherapy.
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页码:2994 / 3006
页数:13
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