纵向血浆代谢组学指导食管鳞状细胞癌化疗免疫治疗的动态风险评估与饮食调节
Longitudinal Plasma Metabolomics Guides Dynamic Risk Assessment and Dietary Modulation for Esophageal Squamous Cell Cancer Chemoimmunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Epigenetically associated CCL20 upregulation correlates with esophageal cancer progression and immune disorder.
Epigenetically associated CCL20 upregulation correlates with esophageal cancer progression and immune disorder.
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趋化因子通过影响癌症免疫和肿瘤发生,对肿瘤进展产生不同影响。然而,在食管癌中,特征性趋化因子谱及其在免疫细胞募集和癌细胞生物学中的作用尚未完全明确。在此,我们仔细研究了独立食管癌队列中趋化因子的表达谱,并确定CCL20升高是预测患者预后的危险因素,且不受组织学亚型影响。CCL20表达增强也与转移潜能的获得相关。在机制上,肿瘤细胞中CCL20的上调与启动子低甲基化相关。此外,通过分析模拟人类ESCC发展的小鼠模型的单细胞RNA测序数据,我们观察到肿瘤微环境中CD4+ T亚型之间的失衡,即在肿瘤发生过程中,异常上皮细胞中Ccl20表达升高的同时伴有Ccr6+ Th17和Treg细胞浸润。总之,这些结果揭示低甲基化诱导的CCL20促进食管癌进展和免疫紊乱。靶向CCL20可能是食管癌中一种有前景的治疗方法。
Chemokines have distinct effects on tumor progression by affecting cancer immunity and tumorigenesis.
However, the characteristic chemokine profiles and their roles in immune cell recruitment and cancer cell biology are not entirely understood in esophageal cancer.
Here, we scrutinized chemokine's expression profiles in independent esophageal cancer cohorts and identified the elevated CCL20 as a risk factor to predict patients' prognosis regardless of histology subtypes. Enhanced CCL20 expression was also associated with the acquisition of metastatic potential.
Mechanistically, the upregulation of CCL20 in tumor cells was associated with promoter hypomethylation.
Furthermore, by analyzing single-cell RNA sequencing data of a mouse model mimicking human ESCC development, we observed an imbalance among CD4 + T subtypes in the tumor microenvironment, namely Ccr6 + Th17 and Treg cells infiltration alongside the elevated Ccl20 expression in abnormal epithelial cells during the tumorigenic process.
Together, these results reveal that hypomethylation-induced CCL20 promotes esophageal cancer progression and immune disorder. Targeting CCL20 might be a promising therapeutic approach in esophageal cancer.
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