Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China; Lung Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Graduate School of Biomedical Sciences, UT MD Anderson Cancer Center, Houston, TX 77030, USA.
Cytokine Growth Factor Rev. 2024 Feb;75:101-109. doi: 10.1016/j.cytogfr.2023.08.004. Epub 2023 Aug 20.
Ferroptosis is a type of cell death characterized by iron-dependent phospholipid peroxidation and reactive oxygen species overproduction. Ferroptosis induces immunogenic cell death and elicits anti-tumor immune responses, playing an important role in cancer immunotherapy. Ferroptosis suppression in cancer cells impairs its immunotherapeutic efficacy. To overcome this issue, ferroptosis inducers (FINs) have been combined with other cancer therapies to create an anti-tumor immune microenvironment. However, the ferroptosis-based crosstalk between immune and tumor cells is complex because oxidative products released by ferroptotic tumor cells impair the functions of anti-tumor immune cells, resulting in immunotherapeutic resistance. In the present article, we have reviewed ferroptosis in tumor and immune cells and summarized the crosstalk between ferroptotic tumor cells and the immune microenvironment. Based on the existing literature, we have further discussed future perspectives on opportunities for combining ferroptosis-targeted therapies with cancer immunotherapies.
铁死亡是一种细胞死亡方式,其特征是铁依赖性磷脂过氧化和活性氧过度产生。铁死亡诱导免疫原性细胞死亡并引发抗肿瘤免疫反应,在癌症免疫治疗中发挥着重要作用。在癌细胞中抑制铁死亡会损害其免疫治疗效果。为了克服这个问题,铁死亡诱导剂(FINs)已与其他癌症治疗方法相结合,以创造抗肿瘤免疫微环境。然而,由于铁死亡肿瘤细胞释放的氧化产物会损害抗肿瘤免疫细胞的功能,导致免疫治疗抵抗,因此免疫细胞和肿瘤细胞之间基于铁死亡的串扰非常复杂。在本文中,我们综述了肿瘤细胞和免疫细胞中的铁死亡,并总结了铁死亡肿瘤细胞与免疫微环境之间的串扰。基于现有文献,我们进一步讨论了将铁死亡靶向治疗与癌症免疫治疗相结合的未来前景。