Identification of EMT-Related Gene Signatures to Predict the Prognosis of Patients With Endometrial Cancer

被引:22
|
作者
Cai, Luya [1 ]
Hu, Chuan [2 ]
Yu, Shanshan [3 ]
Liu, Lixiao [1 ]
Zhao, Jinduo [1 ]
Zhao, Ye [1 ]
Lin, Fan [4 ]
Du, Xuedan [3 ]
Yu, Qiongjie [3 ]
Xiao, Qinqin [5 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, Wenzhou, Peoples R China
[2] Qingdao Univ, Affiliated Hosp, Dept Orthopaed Surg, Qingdao, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp 1, Dept Chemoradiat Oncol, Wenzhou, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 1, Dept Dermatol, Wenzhou, Peoples R China
[5] Wenzhou Med Univ, Affiliated Hosp 1, Dept Radiol, Wenzhou, Peoples R China
关键词
endometrial cancer; EMT; prognosis; gene signature; nomogram; EPITHELIAL-MESENCHYMAL TRANSITION; VARIABLE SELECTION; EXPRESSION; GROWTH; INVASION; ONECUT2; CELLS; MODEL;
D O I
10.3389/fgene.2020.582274
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Endometrial cancer (EC) is one of the most common gynecological cancers. Epithelial-mesenchymal transition (EMT) is believed to be significantly associated with the malignant progression of tumors. However, there is no relevant study on the relationship between EMT-related gene (ERG) signatures and the prognosis of EC patients. Methods We extracted the mRNA expression profiles of 543 tumor and 23 normal tissues from The Cancer Genome Atlas database. Then, we selected differentially expressed ERGs (DEERGs) among these mRNAs. Next, univariate and multivariate Cox regression analyses were performed to select the ERGs with predictive ability for the prognosis of EC patients. In addition, risk score models were constructed based on the selected genes to predict patients' overall survival (OS), progression-free survival (PFS), and disease-free survival (DFS). Finally, nomograms were constructed to estimate the OS and PFS of EC patients, and pan-cancer analysis was performed to further analyze the functions of a certain gene. Results Six OS-, ten PFS-, and five DFS-related ERGs were obtained. By constructing the prognostic risk score model, we found that the OS, PFS, and DFS of the high-risk group were notably poorer. Last, we found that AQP5 appeared in all three gene signatures, and through pan-cancer analysis, it was also found to play an important role in immunity in lower grade glioma (LGG), which may contribute to the poor prognosis of LGG patients. Conclusions We constructed ERG signatures to predict the prognosis of EC patients using bioinformatics methods. Our findings provide a thorough understanding of the effect of EMT in patients with EC and provide new targets and ideas for individualized treatment, which has important clinical significance.
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页数:14
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