| Literature DB >> 33962392 |
Zhou-Tong Dai1, Yuan Xiang1,2, Yundan Wang1, Le-Yuan Bao1, Jun Wang1, Jia-Peng Li1, Hui-Min Zhang1, Zhongxin Lu2, Sreenivasan Ponnambalam3, Xing-Hua Liao1.
Abstract
Bladder cancer (BLCA) is one of the common malignant tumors of the urinary system. The poor prognosis of BLCA patients is due to the lack of early diagnosis and disease recurrence after treatment. Increasing evidence suggests that gene products of the nuclear factor of activated T-cells (NFAT) family are involved in BLCA progression and subsequent interaction(s) with immune surveillance. In this study, we carried out a pan-cancer analysis of the NFAT family and found that NFAT2 is an independent prognostic factor for BLCA. We then screened for differentially expressed genes (DEGs) and further analyzed such candidate gene loci using gene ontology enrichment to curate the KEGG database. We then used Lasso and multivariate Cox regression to identify 4 gene loci (FER1L4, RNF128, EPHB6, and FN1) which were screened together with NFAT2 to construct a prognostic model based on using Kaplan-Meier analysis to predict the overall survival of BLCA patients. Moreover, the accuracy of our proposed model is supported by deposited datasets in the Gene Expression Omnibus (GEO) database. Finally, a nomogram of this prognosis model for BLCA was established which could help to provide better disease management and treatment.Entities:
Keywords: NFAT; bladder cancer; nomogram; overall survival; prognostic risk score
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Year: 2021 PMID: 33962392 PMCID: PMC8202856 DOI: 10.18632/aging.202982
Source DB: PubMed Journal: Aging (Albany NY) ISSN: 1945-4589 Impact factor: 5.682