Integrative Analysis of Multi-Omic Data for the Characteristics of Endometrial Cancer

被引:1
作者
Li, Tong [1 ]
Ruan, Zhijun [2 ]
Song, Chunli [3 ]
Yin, Feng [3 ]
Zhang, Tuanjie [2 ]
Shi, Liyun [1 ]
Zuo, Min [4 ]
Lu, Linlin [5 ]
An, Yuhao [2 ]
Wang, Rui [2 ]
Ye, Xiyang [1 ]
机构
[1] Shenzhen Peoples Hosp, Dept Gynecol, Shenzhen 518020, Guangdong, Peoples R China
[2] Pingshan Translat Med Ctr, Shenzhen Bay Lab, Shenzhen 518118, Peoples R China
[3] Peking Univ, Sch Chem Biol & Biotechnol, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China
[4] Shenzhen Peoples Hosp, Dept Pathol, Shenzhen 518020, Guangdong, Peoples R China
[5] Guangzhou Univ Chinese Med, Int Inst Translat Chinese Med, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
ATYPICAL HYPERPLASIA; PROTEIN; MANAGEMENT; PATHWAY; KINASE;
D O I
10.1021/acsomega.4c00375
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Endometrial cancer (EC) is a frequently diagnosed gynecologic cancer. Identifying reliable prognostic genes for predicting EC onset is crucial for reducing patient morbidity and mortality. Here, a comprehensive strategy with transcriptomic and proteomic data was performed to measure EC's characteristics. Based on the publicly available RNA-seq data, death-associated protein kinase 3, recombination signal-binding protein for the immunoglobulin kappa J region, and myosin light chain 9 were screened out as potential biomarkers that affect the EC patients' prognosis. A linear model was further constructed by multivariate Cox regression for the prediction of the risk of being malignant. From further integrative analysis, exosomes were found to have a highly enriched role that might participate in EC occurrence. The findings were validated by qRT-polymerase chain reaction (PCR) and western blotting. Collectively, we constructed a prognostic-gene-based model for EC prediction and found that exosomes participate in EC incidents, revealing significantly promising support for the diagnosis of EC.
引用
收藏
页码:14489 / 14499
页数:11
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