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Published in: Radiation Oncology 1/2013

Open Access 01-12-2013 | Research

Livin expression is an independent factor in rectal cancer patients with or without preoperative radiotherapy

Authors: Zhen-Yu Ding, Hong Zhang, Gunnar Adell, Birgit Olsson, Xiao-Feng Sun

Published in: Radiation Oncology | Issue 1/2013

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Abstract

Background

This study was aimed to investigate the expression significance of Livin in relation to radiotherapy (RT), clinicopathological and biological factors of rectal cancer patients.

Methods

This study included 144 primary rectal cancer patients who participated in a Swedish clinical trial of preoperative radiotherapy. Tissue microarray samples from the excised primary rectal cancers, normal mucosa and lymph node metastases were immunostained with Livin antibody. The proliferation of colon cancer cell lines SW620 and RKO was assayed after Livin knock-down.

Results

The expression of Livin was significantly increased from adjacent (P = 0.051) or distant (P = 0.028) normal mucosa to primary tumors. 15.4% (2/13) and 39.7% (52/131) patients with Livin-negative and positive tumors died at 180 months after surgery, and the difference tended to be statistically significant (P = 0.091). In multivariate analyses, the difference achieved statistical significance, independent of TNM stage, local and distant recurrence, grade of differentiation, gender, and age (odds ratio = 5.09, 95% CI: 1.01-25.64, P = 0.048). The in vitro study indicated colon cancer cells with Livin knock-down exhibited decreased proliferation compared with controls after RT.

Conclusions

The expression of Livin was was independently related to survival in rectal cancer patients, suggesting Livin as a useful prognostic factor for rectal cancer patients.
Appendix
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Metadata
Title
Livin expression is an independent factor in rectal cancer patients with or without preoperative radiotherapy
Authors
Zhen-Yu Ding
Hong Zhang
Gunnar Adell
Birgit Olsson
Xiao-Feng Sun
Publication date
01-12-2013
Publisher
BioMed Central
Published in
Radiation Oncology / Issue 1/2013
Electronic ISSN: 1748-717X
DOI
https://doi.org/10.1186/1748-717X-8-281

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