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:Glucose-Restricted Diet Regulates the Tumor Immune Microenvironment and Prevents Tumor Growth in Lung Adenocarcinoma.
Glucose-Restricted Diet Regulates the Tumor Immune Microenvironment and Prevents Tumor Growth in Lung Adenocarcinoma.
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这些结果表明,限制葡萄糖饮食可改善宿主肺部免疫反应,并抑制实验性肺腺癌中的肿瘤生长。由于 LUAD 患者的葡萄糖水平与术后生存率呈负相关,限制葡萄糖饮食成为 LUAD 患者的一种治疗途径。
肺癌是西方国家第二常见的癌症类型,死亡率高。在肿瘤的发生和进展过程中,其环境中的营养物质起着核心作用。肿瘤细胞严重依赖葡萄糖代谢和摄取。肿瘤细胞代谢以Warburg效应为主,即在有氧条件下,肿瘤细胞从丙酮酸产生大量乳酸。因此,我们推断,减少饮食中的碳水化合物可能支持当前免疫疗法的抗肿瘤效果,并额外靶向肿瘤免疫逃逸。
减少碳水化合物以改善当前免疫治疗之间的联系尚不明确。因此,我们旨在分析不同葡萄糖水平对肿瘤发生、进展及抗肿瘤免疫反应的影响。
我们将LUAD队列的临床参数与不同代谢标志物进行了相关性分析。此外,我们在不同葡萄糖水平下对A549肿瘤细胞系进行了细胞培养实验。最后,我们在实验性小鼠肺癌模型中研究了低碳水化合物和高碳水化合物饮食对肿瘤进展及不同免疫亚群的影响。
我们发现,肺腺癌(LUAD)患者肺部肿瘤区域中,体重指数(BMI)、血糖水平、总生存期(OS)缩短与胰岛素样生长因子-1受体(IGF1R)表达之间存在正相关。此外,增加细胞外葡萄糖可诱导A549 LUAD细胞中IGF1R的表达。在LUAD小鼠模型中的功能研究表明,葡萄糖限制饮食导致体内肿瘤负荷减少。这一发现与肺浸润性细胞毒性CD8+效应记忆T细胞(TEM)、组织驻留记忆T细胞(TRM)和NK 细胞的存在增加以及IGFR mRNA表达降低相关,提示葡萄糖限制调节肿瘤微环境中的肺部免疫。
Lung cancer is the second common cancer type in western countries and has a high mortality. During the development and progression of the tumor, the nutrients in its environment play a central role. The tumor cells depend crucially on glucose metabolism and uptake. Tumor cell metabolism is dominated by the Warburg effect, where tumor cells produce large amounts of lactate from pyruvate under aerobic conditions. We thus reasoned that, reducing carbohydrates in the diet might support anti-tumoral effects of current immunotherapy and additionally target tumor immune escape.
The link between reducing carbohydrates to improve current immunotherapy is not clear. We thus aimed at analyzing the effects of different glucose levels on the tumor development, progression and the anti-tumoral immune response.
We correlated the clinical parameters of our LUAD cohort with different metabolic markers. Additionally, we performed cell culture experiments with A549 tumor cell line under different glucose levels. Lastly, we investigated the effect of low and high carbohydrate diet in an experimental murine model of lung cancer on the tumor progression and different immune subsets.
Here we found a positive correlation between the body mass index (BMI), blood glucose levels, reduced overall survival (OS) and the expression of Insulin-like growth factor-1 receptor (IGF1R) in the lung tumoral region of patients with lung adenocarcinoma (LUAD). Furthermore, increasing extracellular glucose induced IGF1R expression in A549 LUAD cells. Functional studies in a murine model of LUAD demonstrated that, glucose restricted diet resulted in decreased tumor load in vivo . This finding was associated with increased presence of lung infiltrating cytotoxic CD8+ T effector memory (TEM), tissue resident memory T (TRM) and natural killer cells as well as reduced IGFR mRNA expression, suggesting that glucose restriction regulates lung immunity in the tumor microenvironment.
These results indicate that, glucose restricted diet improves lung immune responses of the host and suppresses tumor growth in experimental lung adenocarcinoma. As glucose levels in LUAD patients were negatively correlated to postoperative survival rates, glucose-restricted diet emerges as therapeutic avenue for patients with LUAD.
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