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Prognostic significance of survivin expression and combined analysis with cancer stem cell and epithelial–mesenchymal transition-related markers in patients with rectal cancer undergoing preoperative chemoradiotherapy

Title
Prognostic significance of survivin expression and combined analysis with cancer stem cell and epithelial–mesenchymal transition-related markers in patients with rectal cancer undergoing preoperative chemoradiotherapy
Authors
Kim J.Ahn S.Kim K.Cho M.S.Kim K.H.Lee R.-A.Nam E.M.
Ewha Authors
김광호조민선이령아남은미김규보
SCOPUS Author ID
김광호scopus; 조민선scopus; 이령아scopus; 남은미scopusscopus; 김규보scopus
Issue Date
2018
Journal Title
Anticancer Research
ISSN
0250-7005JCR Link
Citation
Anticancer Research vol. 38, no. 12, pp. 6881 - 6889
Keywords
Cancer stem cellEpithelial–mesenchymal transitionImmunohistochemistryPreoperative chemoradiotherapyRectal cancerSurvivin
Publisher
International Institute of Anticancer Research
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
Abstract
Aim: To identify the candidate marker predicting treatment response and survival outcome in rectal cancer patients who received preoperative chemoradiotherapy (CRT). Patients and Methods: Between 2000 and 2015, 159 patients with histologically-confirmed rectal adenocarcinoma underwent preoperative CRT followed by surgery. Among them, 70 patients were enrolled and the expression of survivin, cancer stem cell markers (CD44 and CD133) and epithelial–mesenchymal transition markers (E-cadherin and TWIST1) in pretreatment biopsy specimens were evaluated by immunohistochemistry. Associations between the expression of markers and clinical outcomes were evaluated. Results: The median follow-up period of all patients was 71 (range=15-203) months. Five-year overall (OS), disease-free (DFS), locoregional recurrence-free (LRRFS) and distant metastasis-free (DMFS) survival were 80.5%, 60.2% 90.1% and 76.5%, respectively. A significant association between survivin overexpression and worse treatment outcome was shown on univariate analyses for OS, DFS and DMFS (p=0.022, 0.002, and 0.005, respectively). On multivariate analysis, survivin overexpression was an adverse prognosticator for DFS and DMFS (p=0.007 and 0.015, respectively), with a borderline significant trend towards a shorter OS (p=0.069). Four other single biomarkers were not associated with survival outcomes. However, overexpression of both survivin and CD44 was significantly associated with worse OS on multivariate analysis (p=0.003). Conclusion: Survivin combined with CD44 might be a candidate biomarker for the prediction of recurrence and survival in patients who received preoperative CRT for rectal cancer. Further research with a larger population is needed to validate these results. © 2018 International Institute of Anticancer Research. All rights reserved.
DOI
10.21873/anticanres.13064
Appears in Collections:
의과대학 > 의학과 > Journal papers
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