Identification of Tumor Microenvironment-Related Alternative Splicing Events to Predict the Prognosis of Endometrial Cancer

被引:4
|
作者
Liu, Xuan [1 ]
Liu, Chuan [2 ]
Liu, Jie [3 ]
Song, Ying [3 ]
Wang, Shanshan [3 ]
Wu, Miaoqing [3 ]
Yu, Shanshan [4 ]
Cai, Luya [5 ]
机构
[1] Jinhua Peoples Hosp, Dept Obstet & Gynecol, Jinhua, Zhejiang, Peoples R China
[2] China Med Univ, Hosp 1, Dept Med Oncol, Shenyang, Peoples R China
[3] Jinhua Peoples Hosp, Dept Gynecol, Jinhua, Zhejiang, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 1, Dept Chemoradiat Oncol, Wenzhou, Peoples R China
[5] Wenzhou Med Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, Wenzhou, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2021年 / 11卷
关键词
endometrial cancer; alternative splicing; tumor microenvironment; prognosis; gene signature; CELL; EXPRESSION;
D O I
10.3389/fonc.2021.645912
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Endometrial cancer (EC) is one of the most common female malignant tumors. The immunity is believed to be associated with EC patients' survival, and growing studies have shown that aberrant alternative splicing (AS) might contribute to the progression of cancers. Methods We downloaded the clinical information and mRNA expression profiles of 542 tumor tissues and 23 normal tissues from The Cancer Genome Atlas (TCGA) database. ESTIMATE algorithm was carried out on each EC sample, and the OS-related different expressed AS (DEAS) events were identified by comparing the high and low stromal/immune scores groups. Next, we constructed a risk score model to predict the prognosis of EC patients. Finally, we used unsupervised cluster analysis to compare the relationship between prognosis and tumor immune microenvironment. Results The prognostic risk score model was constructed based on 16 OS-related DEAS events finally identified, and then we found that compared with high-risk group the OS in the low-risk group was notably better. Furthermore, according to the results of unsupervised cluster analysis, we found that the better the prognosis, the higher the patient's ESTIMATE score and the higher the infiltration of immune cells. Conclusions We used bioinformatics to construct a gene signature to predict the prognosis of patients with EC. The gene signature was combined with tumor microenvironment (TME) and AS events, which allowed a deeper understanding of the immune status of EC patients, and also provided new insights for clinical patients with EC.
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页数:12
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