RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Induced Necroptosis and Its Role in Cancer Immunotherapy.
Induced Necroptosis and Its Role in Cancer Immunotherapy.
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坏死性凋亡是一种受调控的细胞死亡(RCD),由某些死亡受体感知细胞外或细胞内环境变化而触发。由于其具有诱导免疫应答和克服凋亡抵抗的强大能力,它作为潜在的癌症治疗手段受到了广泛关注。对肿瘤坏死性凋亡机制的研究为纳米生物医学疗法的创建提供了基础信息。受体相互作用蛋白激酶1(RIPK1)-RIPK3介导的坏死性凋亡、含Toll样受体结构域的接头诱导干扰素(IFN)-β(TRIF)-RIPK3介导的坏死性凋亡、Z-DNA结合蛋白1(ZBP1)-RIPK3介导的坏死性凋亡以及IFNR介导的坏死性凋亡是本综述中共同解释触发坏死性凋亡的四条信号通路。坏死性凋亡作为一种可能的癌症治疗策略引起了极大兴趣,因为与凋亡不同,它能引发与治疗相关的免疫应答。
因此,本文对肿瘤细胞坏死性凋亡与免疫环境、癌症免疫监视以及树突状细胞(DCs)、细胞毒性T细胞、自然杀伤(NK)细胞、自然杀伤T(NKT)细胞等细胞及其各自细胞因子之间的联系进行了深入讨论。
最后,本文总结了最新诱导坏死性凋亡以引发免疫原性细胞死亡的纳米药物,以强调其在癌症免疫治疗中的前景。
Necroptosis is a type of regulated cell death (RCD) that is triggered by changes in the extracellular or intracellular milieu that are picked up by certain death receptors. Thanks to its potent capacity to induce immunological responses and overcome apoptotic resistance, it has garnered significant attention as a potential cancer treatment. Basic information for the creation of nano-biomedical treatments is provided by studies on the mechanisms underlying tumor necroptosis.
Receptor-interacting protein kinase 1 (RIPK1)-RIPK3-mediated necroptosis, Toll-like receptor domain-containing adapter-inducing interferon (IFN)-β (TRIF)-RIPK3-mediated necroptosis, Z-DNA-binding protein 1 (ZBP1)-RIPK3-mediated necroptosis, and IFNR-mediated necroptosis are the four signaling pathways that collectively account for triggered necroptosis in this review. Necroptosis has garnered significant interest as a possible cancer treatment strategy because, in contrast to apoptosis, it elicits immunological responses that are relevant to therapy.
Thus, a thorough discussion is held on the connections between tumor cell necroptosis and the immune environment, cancer immunosurveillance, and cells such as dendritic cells (DCs), cytotoxic T cells, natural killer (NK) cells, natural killer T (NKT) cells, and their respective cytokines. Lastly, a summary of the most recent nanomedicines that cause necroptosis in order to cause immunogenic cell death is provided in order to emphasize their promise for cancer immunotherapy.
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