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Published in: Journal of Translational Medicine 1/2013

Open Access 01-12-2013 | Research

CDC20 overexpression predicts a poor prognosis for patients with colorectal cancer

Authors: Wen-jing Wu, Kai-shun Hu, De-shen Wang, Zhao-lei Zeng, Dong-sheng Zhang, Dong-liang Chen, Long Bai, Rui-hua Xu

Published in: Journal of Translational Medicine | Issue 1/2013

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Abstract

Background

The cell division cycle 20 homolog (CDC20) is an essential cofactor of the anaphase-promoting complex (APC/C). CDC20 overexpression has been detected in many types of human cancers; however, its clinical role in colorectal cancer remains unknown.

Methods

Western blotting and immunohistochemistry were used to compare CDC20 expression in adjacent non-cancerous, cancerous and liver metastatic tissues as well as in colon cancer cell lines and normal colon epithelial cell lines. Additionally, the correlation of CDC20 expression with patient clinical parameters and its diagnostic value were statistically analyzed.

Results

CDC20 was overexpressed in colon cancer cell lines/primary cancer tissues compared with normal colon epithelial cell lines/adjacent noncancerous tissue samples. Interestingly, CDC20 expression was further increased in metastatic liver tissues. CDC20 protein expression was significantly correlated with clinical stage (P = 0.008), N classification (P = 0.020), M classification (P = 0.013) and pathologic differentiation (P = 0.008). Patients with higher CDC20 expression had a shorter overall survival than those with lower CDC20 expression. Univariate and multivariate analyses indicated that CDC20 expression was an independent prognostic factor (P < 0.001).

Conclusion

CDC20 may serve as a potential prognostic biomarker of human colorectal cancer.
Appendix
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Metadata
Title
CDC20 overexpression predicts a poor prognosis for patients with colorectal cancer
Authors
Wen-jing Wu
Kai-shun Hu
De-shen Wang
Zhao-lei Zeng
Dong-sheng Zhang
Dong-liang Chen
Long Bai
Rui-hua Xu
Publication date
01-12-2013
Publisher
BioMed Central
Published in
Journal of Translational Medicine / Issue 1/2013
Electronic ISSN: 1479-5876
DOI
https://doi.org/10.1186/1479-5876-11-142

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