Abstract

BackgroundGallbladder cancer (GBC) is the most common biliary tract malignancy and has a poor prognosis in patients with GBC. CircRNA TP63 (circTP63) has been implicated in cell proliferation and invasion in some tumor progress. The study aims to investigate the clinical significance and functional role of circTP63 expression in GBC.MethodsThe expression of circTP63 in GBC tissues or cells was detected by qRT-PCR and the association between circTP63 expression and prognosis of GBC patients was analyzed. CCK8 assay, flow cytometry analysis, transwell assay and in vivo studies were used to evaluate the cell proliferation and invasion abilities after circTP63 knockdown in GBC cells. Luciferase reporter assays and RNA pull-down assay were used to determine the correlation between circTP63 and miR-217 expression. Besides, western blot analysis was also performed.ResultsIn the present study, we showed that circTP63 expression was upregulated in GBC tissues and cells. Higher circTP63 expression was associated with lymph node metastasis and short overall survival (OS) in patients with GBC. In vitro, knockdown of circTP63 significantly inhibited cell proliferation, cell cycle progression, migration and invasion abilities in GBC. Besides, we demonstrated that knockdown of circTP63 inhibited GBC cells Epithelial-Mesenchymal Transition (EMT) process. In vivo, knockdown of circTP63 inhibited tumor growth in GBC. Mechanistically, we demonstrated that circTP63 competitively bind to miR-217 and promoted EZH2 expression and finally facilitated tumor progression.ConclusionsOur findings demonstrated that circTP63 sponged to miR-217 and regulated EZH2 expression and finally facilitated tumor progression in GBC. Thus, targeting circTP63 may be a therapeutic strategy for the treatment of GBC.

Highlights

  • Gallbladder cancer (GBC) is one of the most common digestive tract tumors worldwide [1]

  • CircTP63 expression is upregulated in GBC and correlates with poor prognosis To explore the clinical significance of circTP63 expression in GBC, we detected the circTP63 expression collected from 39 pairs of GBC tissues and adjacent normal tissues by Quantitative real-time PCR (qRT-PCR)

  • The results showed that circTP63 expression was dramatically upregulated compared with adjacent normal tissues in patients with GBC (Fig. 1A)

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Summary

Introduction

Gallbladder cancer (GBC) is one of the most common digestive tract tumors worldwide [1]. Most gallbladder cancer patients have an extremely poor prognosis, and the 5-year overall survival rate is less than 5% [4]. Wang et al Cancer Cell International (2021) 21:608 found that molecular targeted therapeutics including fibroblast growth factor receptor (FGFR), MEK, ERBB2 or PI3-Kinase inhibitors have been explored, which provide hope for gallbladder cancer treatment [5]. Elucidating the mechanism of the occurrence and development and validating existing novel molecular target to improve therapeutic effects of GBC patients are needed. Gallbladder cancer (GBC) is the most common biliary tract malignancy and has a poor prognosis in patients with GBC. The study aims to investigate the clinical significance and functional role of circTP63 expression in GBC

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