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:Glycerol kinase enzyme is a prognostic predictor in esophageal carcinoma and is associated with immune cell infiltration.
Glycerol kinase enzyme is a prognostic predictor in esophageal carcinoma and is associated with immune cell infiltration.
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脂质代谢对肿瘤发生和进展的影响已引起广泛关注。然而,甘油代谢中的关键酶甘油激酶(GK)在食管癌(ESCA)中的作用仍不清楚。为进一步阐明GK与ESCA之间的关系,我们利用数据库信息研究了GK的表达水平。对临床ESCA肿瘤样本和正常标本进行了采用免疫组化的对照研究,证实了GK在ESCA中表达升高。通过Kaplan-Meier(KM)生存曲线分析癌症基因组图谱(TCGA)数据发现,GK表达升高与ESCA患者较差的预后相关,尤其是在总生存期(OS)和疾病特异性生存期(DSS)方面。多元回归分析表明,GK表达升高是影响ESCA预后的独立危险因素。对临床样本预后数据的统计分析进一步证实了这一发现。此外,GK表达与免疫浸润之间似乎存在显著相关性,具体涉及某些T淋巴细胞和B淋巴细胞。总之,ESCA中GK表达升高与不良预后和免疫细胞浸润增加密切相关,凸显了其作为独立预后生物标志物和可行治疗靶点的潜力。
The influence of lipid metabolism on tumorigenesis and progression has garnered significant attention.
However, the role of Glycerol Kinase (GK), a key enzyme in glycerol metabolism, in Esophageal Carcinoma (ESCA) remains unclear. To further elucidate the relationship between GK and ESCA, we investigated GK expression levels using database information. Controlled studies employing immunohistochemistry were conducted on clinical ESCA tumor samples and normal specimens, confirming GK's elevated expression in ESCA.
Analysis of The Cancer Genome Atlas (TCGA) data via Kaplan-Meier (KM) survival plots revealed that increased GK expression correlates with poorer ESCA patient outcomes, particularly in overall survival (OS) and disease-specific survival (DSS). Multiple regression analysis indicated that elevated GK expression is an independent risk factor affecting ESCA prognosis. Statistical analysis of prognostic data from clinical samples further corroborated this finding.
Moreover, there appears to be a significant correlation between GK expression and immune infiltration, specifically involving certain T and B lymphocytes.
In conclusion, elevated GK expression in ESCA is strongly linked to poor prognosis and increased immune cell infiltration, highlighting its potential as an independent prognostic biomarker and a viable therapeutic target.
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