Abstract

TFF1, one member of the trefoil factor family (TFFs), is an antiproteinolytic peptide. Abnormal TFF1 expression is associated with carcinogenesis. In order to investigate the expression of TFF1 in esophageal carcinoma and its potential gene regulatory network. We used sequencing data from the Cancer Genome Atlas database and Gene Expression Omnibus, analyzed TFF1 expression and gene regulation networks in esophageal carcinoma (ESCA). TFF1 expression profiling was analyzed using Oncomine TM, while TFF1 mutation and related functional networks were identified using cBioPortal. Linked Omics was used to identify differential gene expression with TFF1 and to analyze Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathways. We found that TFF1 is overexpressed in ESCA, and deletion is the most common TFF1 mutation type in ESCA, and TFF1 gene mutation may also significantly affect the prognosis of ESCA patients. Functional network analysis showed that TFF1 may play a role in ESCA by participating in NF-κB signaling pathway and Hippo signaling pathway. Our results demonstrate that data mining efficiently reveals information about TFF1 expression and potential regulatory networks in ESCA, laying a foundation for further study of the role of TFF1 in carcinogenesis.

Highlights

  • Esophageal carcinoma (ESCA) has been ranked the seventh position in the world cancer incidence rate, and the mortality rate is sixth [1]

  • Our results here show that in esophageal carcinoma (ESCA) patients, TFF1 is overexpressed, and its mRNA expression is significantly correlated with the individual cancer stage of patients

  • Functional network analysis shows that TFF1 may play a role in ESCA by participating in the NF-κB signal pathway and Hippo signal pathway

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Summary

Introduction

Esophageal carcinoma (ESCA) has been ranked the seventh position in the world cancer incidence rate, and the mortality rate is sixth [1]. The prognosis of patients with ESCA is miserable due to late diagnosis and poor response to treatment, and the limit of 5-year survival rate is 15% [4,8,9,10]. A number of researches in different tumor tissues, including colon, pancreatic, and ovarian cancer, have indicated that the survival, invasion, and metastasis of tumor cells may be regulated by TFF1 [18,19,20]. TFF1 knockout mice have a high incidence of pyloric adenoma, in this trend, 30% of them boosted malignant gastric cancer [21] These previous results suggest that TFF1 may be a new tumor marker. Our findings may provide novel biomarkers and strategies fronting early diagnosing and intervention of ESCA

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