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Prognostic value of epithelial-mesenchymal transition markers in clear cell renal cell carcinoma
Author(s) -
Hua Xu,
Wenhao Xu,
Fei Ren,
Jun Wang,
Hongkai Wang,
Da-Long Cao,
Guo-Hai Shi,
Yuan-Yuan Qu,
HaiLiang Zhang,
Ding-Wei Ye
Publication year - 2020
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.102660
Subject(s) - snai1 , cdh1 , epithelial–mesenchymal transition , clear cell renal cell carcinoma , oncology , proportional hazards model , medicine , cancer research , cohort , foxa1 , metastasis , cancer , biology , renal cell carcinoma , cell , breast cancer , cadherin , genetics
Epithelial-to-mesenchymal transition (EMT) is important in tumor invasiveness and metastasis. We aimed to determine prognostic value of six key EMT markers ( CDH1 , CDH2 , SNAI1 , SNAI2 , VIM , TWIST1 ) in clear cell renal cell carcinoma (ccRCC). A total of 533 ccRCC patients with RNASeq data from The Cancer Genome Atlas (TCGA) cohort were included for analysis. Gene expression of these EMT markers was compared between tumor and normal tissues based on Oncomine database and TCGA cohort. Their correlations with progression-free survival (PFS) and overall survival (OS) were also examined in both TCGA cohort and FUSCC (Fudan University Shanghai Cancer Center) cohort. Cox proportional hazards regression model and Kaplan-Meier plot were used to assess the relative factors. Functional enrichment analyses were utilized to describe biologic function annotations and significantly involved hallmarks pathways of each gene. We found that Epithelial marker, CDH1 expression was lower, while mesenchymal markers ( CDH2 , SNAI1 , VIM , TWIST1 ) expression was higher in ccRCC primary tumors. In the TCGA cohort, we found that patients with higher expression of VIM , TWIST1 or lower expression of CDH1 had worse prognosis. Further, in the FUSCC cohort, we confirmed the predictive ability of mesenchymal markers and epithelial marker expression in PFS and OS of ccRCC patients. After generating Cox regression models, EMT markers ( CDH1 , SNAI1 , VIM , and TWIST1 ) were independent prognostic factors of both PFS and OS in ccRCC patients. Our preliminary EMT prediction model can facilitate further screening of EMT biomarkers and cast a better understanding of EMT gene function in ccRCC.

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