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:Overcoming immunosuppression in cancer: how ketogenic diets boost immune checkpoint blockade.
Overcoming immunosuppression in cancer: how ketogenic diets boost immune checkpoint blockade.
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免疫检查点阻断(ICB)现已成为多种癌症标准治疗的一部分,但其对部分患者缺乏疗效,因此需要辅助治疗来支持抗肿瘤免疫反应。生酮饮食(KDs),即高脂低碳水化合物饮食,已在多项临床前癌症研究中显示出抗增殖和免疫调节作用。
在此,我们综述了在ICB治疗背景下,关于KDs与抗肿瘤免疫反应复杂相互作用的最新认识,以更新我们对癌症中饮食诱导的免疫代谢重编程的理解。临床前癌症研究显示,在KD方案作用下,抗肿瘤免疫细胞的活化和浸润增加,尤其是CD8+ T细胞,也包括M1巨噬细胞和NK 细胞。相反,在KD喂养小鼠的肿瘤中,免疫抑制性细胞如调节性CD4+ T淋巴细胞、M2巨噬细胞和髓源性抑制细胞被报道减少或基本未受影响。KDs在多项临床前肿瘤研究中也显示出与ICB治疗的协同作用。所观察到的效应被归因于KDs改善免疫细胞浸润并诱导免疫抑制过程下调的能力,从而创造出更具免疫原性的肿瘤微环境。本文综述的研究表明,通过KD改变肿瘤微环境的代谢组成可以增强抗肿瘤免疫反应,甚至削弱免疫治疗耐药以及免疫学“冷”肿瘤。
然而,确切的内在机制仍有待阐明,需要进一步研究才能将KDs成功实施为辅助肿瘤治疗,以提高癌症患者的生存率。
Immune checkpoint blockade (ICB) is now part of the standard of care in the treatment of many forms of cancer, yet it lacks efficacy in some patients, necessitating adjunct therapies to support the anti-tumor immune response. Ketogenic diets (KDs), i. e. , high-fat low-carbohydrate diets, have been shown to have antiproliferative and immunomodulatory effects in various preclinical cancer studies.
Here, we review current knowledge of the complex interplay of KDs and the anti-tumor immune response in the context of ICB therapy, to update our understanding of diet-induced immunometabolic reprogramming in cancer. Preclinical cancer studies have revealed increased activation of and infiltration by tumor-fighting immune cells, especially CD8+ T cells, but also M1 macrophages and natural killer cells, in response to a KD regimen. In contrast, immune-suppressive cells such as regulatory CD4+ T lymphocytes, M2 macrophages, and myeloid-derived suppressor cells were reported to be decreased or largely unaffected in tumors of KD-fed mice.
KDs also showed synergism with ICB therapy in several preclinical tumor studies. The observed effects are ascribed to the ability of KDs to improve immune cell infiltration and induce downregulation of immune-inhibitory processes, thus creating a more immunogenic tumor microenvironment. The studies reviewed herein show that altering the metabolic composition of the tumor microenvironment by a KD can boost the anti-tumor immune response and diminish even immunotherapy-resistant as well as immunologically "cold" tumors.
However, the exact underlying mechanisms remain to be elucidated, requiring further studies before KDs can be successfully implemented as an adjunct tumor therapy to improve survival rates for cancer patients.
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