STK24 expression is modulated by DNA copy number/methylation in lung adenocarcinoma and predicts poor survival

被引:13
|
作者
Huang, Ningyu [1 ]
Lin, Wenbo [1 ]
Shi, Xiuyu [1 ]
Tao, Tao [1 ]
机构
[1] Xiamen Univ, Sch Life Sci, State Key Lab Cellular Stress Biol, Xiamen 361102, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
copy number; lung adenocarcinoma; methylation; prognosis; STK24; 20-LIKE KINASE-3 MST3; PROTEIN-KINASE; CELL-MIGRATION; CANCER; PHOSPHORYLATION; INHIBITION;
D O I
10.2217/fon-2018-0126
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: To explore the independent prognostic value of STK24 expression in terms of overall survival and recurrence-free survival and the potential mechanisms of its dysregulation in non-small-cell lung adenocarcinoma. Patients & methods: Data were from the Cancer Genome Atlas-lung adenocarcinoma. Results: Increased STK24 expression was an independent prognostic indicator of unfavorable overall survival (Hazard ratio: 1.478; 95% CI: 1.149-1.901; p<0.002) and recurrence-free survival (Hazard ratio: 1.855; 95% CI: 1.399-2.458; p<0.001). DNA amplification was associated with significantly upregulated STK24 expression. There was a weak negative correlation between STK24 expression and its DNA methylation (Pearson's r = -0.32). Conclusion: Aberrant STK24 expression was an independent prognostic indicator in lung adenocarcinoma patients. Its dysregulation was associated with its DNA copy number alteration and methylation.
引用
收藏
页码:2253 / 2263
页数:11
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