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铁死亡与癌症免疫治疗

Ferroptosis and Cancer Immunotherapy.

作者信息

Yin Jumei, Meng Xingqi, Peng Lixuan, Xie Wei, Liu Xuan, He Weiguo, Li Suyun

机构信息

Clinical Anatomy and Reproductive Medicine Application Institute, Hengyang Medical School, University of South China, Hengyang 421001, China.

出版信息

Curr Mol Med. 2023;23(5):401-409. doi: 10.2174/1566524022666220509124608.

Abstract

Traditional treatment strategies for cancer are unsatisfactory. As a nonapoptotic cell death process and owning to the characteristics of iron-dependent lipid peroxide accumulation, ferroptosis has become a new target of tumor treatment. Numerous studies have proved that ferroptosis could enhance the immunogenicity of cancer and interact with immune cells. Cancer antigens, exposed to cancer cells that underwent ferroptosis, effectively improve the immunogenicity of the tumor microenvironment and promote the activation and maturation of immune cells. Meantime, immune cells release immunostimulatory cytokines including TNF-α and IFN-γ to downregulate the expression of SLC7A11 and SLC3A2, and reduce the absorption of cysteine, leading to lipid peroxidation and iron deposition in cancer cells. Consequently, induction of ferroptosis via iron deposition-based combination strategies could stimulate and activate natural and adaptive immune responses which release immune-stimulating factors to induce iron deposition in cancer cells. In this review, we provided a critical analysis of the correlation between ferroptosis and the immune responses, providing a novel way to effectively induce ferroptosis in cancer, which may be one of the focuses in future to improve the development of new therapeutic strategies of cancer.

摘要

传统的癌症治疗策略并不令人满意。作为一种非凋亡性细胞死亡过程,且由于铁依赖性脂质过氧化物积累的特性,铁死亡已成为肿瘤治疗的新靶点。大量研究证明,铁死亡可增强癌症的免疫原性并与免疫细胞相互作用。经历铁死亡的癌细胞所暴露的癌症抗原,能有效提高肿瘤微环境的免疫原性,并促进免疫细胞的激活和成熟。同时,免疫细胞释放包括肿瘤坏死因子-α和干扰素-γ在内的免疫刺激细胞因子,以下调溶质载体家族7成员11(SLC7A11)和溶质载体家族3成员2(SLC3A2)的表达,并减少半胱氨酸的摄取,导致癌细胞中的脂质过氧化和铁沉积。因此,通过基于铁沉积的联合策略诱导铁死亡可刺激并激活天然免疫和适应性免疫反应,这些反应会释放免疫刺激因子以诱导癌细胞中的铁沉积。在本综述中,我们对铁死亡与免疫反应之间的相关性进行了批判性分析,提供了一种在癌症中有效诱导铁死亡的新方法,这可能是未来改善癌症新治疗策略发展的重点之一。

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