Abstract

BackgroundPreoperative chemoradiotherapy (CRT) is the cornerstone of treatment for locally advanced rectal cancer (LARC). Although high local control is achieved, overall rates of distant control remain suboptimal. Colorectal carcinogenesis is associated with critical alterations of the Wnt/β-catenin pathway involved in proliferation and survival. The aim of this study was to assess whether CRT induces changes in the expression of β-catenin/E-cadherin, and to determine whether these changes are associated with survival.MethodsThe Immunohistochemical expression of nuclear β-catenin and membranous E-cadherin was prospectively analysed in tumour blocks from 98 stage II/III rectal cancer patients treated with preoperative CRT. Tumour samples were collected before and after CRT treatment. All patients were treated with pelvic RT (46–50 Gy in 2 Gy fractions) and 5-fluorouracil (5FU) intravenous infusion (225 mg/m2) or capecitabine (825 mg/m2) during RT treatment, followed by total mesorectal excision (TME). Disease-free survival (DFS) was analysed using the Kaplan-Meier method and a multivariate Cox regression model was employed for the Multivariate analysis.ResultsCRT induced significant changes in the expression of nuclear β-catenin (49% of patients presented an increased expression after CRT, 17% a decreased expression and 34% no changes; p = 0.001). After a median follow-up of 25 months, patients that overexpressed nuclear β-catenin after CRT showed poor survival compared with patients that experienced a decrease in nuclear β-catenin expression (3-year DFS 92% vs. 43%, HR 0.17; 95% CI 0.03 to 0.8; p = 0.02). In the multivariate analysis for DFS, increased nuclear β-catenin expression after CRT almost reached the cut-off for significance (p = 0.06).ConclusionsIn our study, preoperative CRT for LARC induced significant changes in nuclear β-catenin expression, which had a major impact on survival. Finding a way to decrease CRT resistance would significantly improve LARC patient survival.

Highlights

  • Preoperative chemoradiotherapy (CRT) is the cornerstone of treatment for locally advanced rectal cancer (LARC)

  • High local control is achieved with multi-modality treatment, overall rates of distant control remain suboptimal in 30% of patients, and it is considered the leading cause of treatment failure [1]

  • Colorectal carcinogenesis is associated with critical alterations of the Wnt/β-catenin signalling pathway [2]. β-catenin is a key multifunctional adaptor protein harbouring functions that are related to the subcellular location [3]

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Summary

Introduction

Preoperative chemoradiotherapy (CRT) is the cornerstone of treatment for locally advanced rectal cancer (LARC). High local control is achieved, overall rates of distant control remain suboptimal. Colorectal carcinogenesis is associated with critical alterations of the Wnt/β-catenin pathway involved in proliferation and survival. The aim of this study was to assess whether CRT induces changes in the expression of β-catenin/E-cadherin, and to determine whether these changes are associated with survival. Preoperative chemoradiotherapy (CRT) is the standard treatment for locally advanced rectal cancer (LARC). High local control is achieved with multi-modality treatment, overall rates of distant control remain suboptimal in 30% of patients, and it is considered the leading cause of treatment failure [1]. Colorectal carcinogenesis is associated with critical alterations of the Wnt/β-catenin signalling pathway [2]. Β-catenin associates with members of the TCF-LEF family of transcription factors and activates the expression of target genes that enhance proliferation and cell survival. β-catenin is controlled by a multi-protein degradation complex, which contains the tumour suppressor adenomatous polyposis coli (APC), Axin, glycogen synthase kinase 3β (GSK3β) and casein kinase I [2,4]

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