Screening and Verification of TPM1 and CALD1 Related to Diagnosis and Prognosis of Bladder Cancer
10.3971/j.issn.1000-8578.2021.20.1536
- VernacularTitle:膀胱癌诊断与预后相关基因TPM1和CALD1的筛选及验证
- Author:
Yang ZHAO
1
;
Fujiang CHANG
;
Lei GE
;
Nan ZHANG
;
Zhongjie SHAN
Author Information
1. Department of Urinary Surgery, People's Hospital of Zhengzhou, Zhengzhou 450000, China
- Publication Type:Research Article
- Keywords:
Bladder cancer;
Bioinformatics analysis;
Prognosis;
Diagnosis;
Tumor progression;
External experimental verification
- From:
Cancer Research on Prevention and Treatment
2021;48(9):827-832
- CountryChina
- Language:Chinese
-
Abstract:
Objective To screen and verify hub genes TPM1 and CALD1 that can affect the diagnosis and prognosis of bladder cancer (BLCA). Methods We obtained gene chip expression data of 414 and 188 cases of bladder cancer from TCGA and GEO, respectively. By constructing a weighted gene co-expression network analysis (WGCNA) and identifying differentially-expressed genes between tumor tissues and normal tissues, the pivotal genes that were highly associated with bladder cancer were obtained, and the STRING database was used to construct a protein interaction network to screen out prognostic-related pivotal genes. We took 29 cases of bladder cancer samples from People's Hospital of Zhengzhou as external verification results. Results A total of 915 and 464 differentially-expressed genes were screened from the TCGA database and GSE13507, respectively. Two modules with the strongest correlation were obtained through WGCNA: the blue module (Pearson cor=0.60, P=1E-44) and the cyan module (Pearson cor=0.52, P=7E-19), and 156 intersection genes were obtained. Through protein interaction network analysis, 10 pivotal genes were screened out. TPM1 and CALD1 genes had the greatest correlation with the survival of bladder cancer patients, which was verified by external experimental verification group. Conclusion TPM1 and CALD1 are closely related to the prognosis of bladder cancer patients. They are also pivotal genes to promote tumor progression.