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胃癌中DGKI的过表达预示预后不良。

Overexpression of DGKI in Gastric Cancer Predicts Poor Prognosis.

作者信息

Huang Chao, Zhao Jiefeng, Luo Chen, Zhu Zhengming

机构信息

Department of Gastrointestinal Surgery, The Second Affiliated Hospital of Nanchang University, Nanchang, China.

出版信息

Front Med (Lausanne). 2020 Jul 7;7:320. doi: 10.3389/fmed.2020.00320. eCollection 2020.

Abstract

Diacylglycerol kinase iota (DGKI) is overexpressed in a variety of cancers and is associated with poor prognosis in colon cancer. This study evaluated the prognostic value of DGKI in gastric cancer (GC) using data from The Cancer Genome Atlas (TCGA). RNA sequencing results and clinical data of gastric adenoma and adenocarcinoma samples were obtained from the TCGA database (https://portal.gdc.cancer.gov). The Wilcoxon or Kruskal-Wallis test and logistic regression were used to analyze the relationship between DGKI and the clinicopathological characteristics of GC patients. Univariate Cox regression and Kaplan-Meier analysis were used to analyze the clinicopathological characteristics of GC patients and the relationship between DGKI and overall survival time, and multivariate Cox regression analysis was used to identify independent risk factors affecting the prognosis of GC patients. Gene set enrichment analysis (GSEA) was performed using the TCGA dataset. DGKI was overexpressed in gastric tumors and was related to poor prognosis ( = 0.003). Overexpression of DGKI in GC was significantly correlated with high grade (OR = 1.71 for G3 vs. G2), stage (OR = 2.08 for II vs. I) and T classification (OR = 4.64 for T4 vs. T1; OR = 3.99 for T3 vs. T1; OR = 3.37 for T2 vs. T1) (all <0.05). DGKI (OR = 7.34; = 0.000) was an independent risk factor affecting the survival of GC patients. The MAPK signaling pathway was differentially enriched with DGKI overexpression. DGKI overexpression may be a potential molecular marker for poor prognosis in GC. The MAPK signaling pathway may be one of the key pathways related to DGKI regulation in GC.

摘要

二酰基甘油激酶ι(DGKI)在多种癌症中过度表达,且与结肠癌的不良预后相关。本研究使用来自癌症基因组图谱(TCGA)的数据评估了DGKI在胃癌(GC)中的预后价值。从TCGA数据库(https://portal.gdc.cancer.gov)获取胃腺瘤和腺癌样本的RNA测序结果及临床数据。采用Wilcoxon或Kruskal-Wallis检验以及逻辑回归分析DGKI与GC患者临床病理特征之间的关系。使用单因素Cox回归和Kaplan-Meier分析GC患者的临床病理特征以及DGKI与总生存时间的关系,并使用多因素Cox回归分析确定影响GC患者预后的独立危险因素。使用TCGA数据集进行基因集富集分析(GSEA)。DGKI在胃肿瘤中过度表达,且与不良预后相关(P = 0.003)。GC中DGKI的过度表达与高分级(G3 vs. G2,OR = 1.71)、分期(II vs. I,OR = 2.08)和T分类(T4 vs. T1,OR = 4.64;T3 vs. T1,OR = 3.99;T2 vs. T1,OR = 3.37)显著相关(均P <0.05)。DGKI(OR = 7.34;P = 0.000)是影响GC患者生存的独立危险因素。MAPK信号通路在DGKI过度表达时差异富集。DGKI过度表达可能是GC预后不良的潜在分子标志物。MAPK信号通路可能是GC中与DGKI调控相关的关键通路之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f9/7358307/9c5e825bbfd6/fmed-07-00320-g0001.jpg

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