Biomarkers discovery for endometrial cancer: A graph convolutional sample network method

被引:2
|
作者
Wu, Erman [1 ]
Fan, Xuemeng [1 ]
Tang, Tong [1 ,4 ]
Li, Jingjing [1 ]
Wang, Jiao [1 ]
Liu, Xingyun [1 ]
Zungar, Zayatta [2 ]
Ren, Jiaojiao [3 ]
Wu, Cong [1 ]
Shen, Bairong [1 ]
机构
[1] Sichuan Univ, West China Hosp, Inst Syst Genet, Frontiers Sci Ctr Dis Related Mol Network, Chengdu, Peoples R China
[2] Univ New England, Sch Med, Armidale, NSW 2351, Australia
[3] Chengdu Univ, Sch Elect Informat & Elect Engn, Chengdu, Peoples R China
[4] Univ A Coruna, Dept Comp Sci & Informat Technol, Elvina Campus, La Coruna, Spain
基金
中国国家自然科学基金;
关键词
Bioinformatics model; Biomarker discovery; Sample network; Graph convolutional network; Endometrial cancer; AURORA KINASE; EXPRESSION; CARCINOMA; GENE; PROGRESSION; PROGNOSIS; AURKA;
D O I
10.1016/j.compbiomed.2022.106200
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Endometrial carcinoma is the sixth most common cancer in women worldwide. Importantly, endometrial cancer is among the few types of cancers with patient mortality that is still increasing, which in-dicates that the improvement in its diagnosis and treatment is still urgent. Moreover, biomarker discovery is essential for precise classification and prognostic prediction of endometrial cancer.Methods: A novel graph convolutional sample network method was used to identify and validate biomarkers for the classification of endometrial cancer. The sample networks were first constructed for each sample, and the gene pairs with high frequencies were identified to construct a subtype-specific network. Putative biomarkers were then screened using the highest degrees in the subtype-specific network. Finally, simplified sample net-works are constructed using the biomarkers for the graph convolutional network (GCN) training and prediction.Results: Putative biomarkers (23) were identified using the novel bioinformatics model. These biomarkers were then rationalised with functional analyses and were found to be correlated to disease survival with network entropy characterisation. These biomarkers will be helpful in future investigations of the molecular mechanisms and therapeutic targets of endometrial cancers. Conclusions: A novel bioinformatics model combining sample network construction with GCN modelling is proposed and validated for biomarker discovery in endometrial cancer. The model can be generalized and applied to biomarker discovery in other complex diseases.
引用
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页数:10
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