Prognostic relevance and therapeutic implications of centromere protein F expression in patients with esophageal squamous cell carcinoma

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Abstract

Centromere protein F (CENP-F), a cell cycle-regulated centromere protein, has been shown to affect numerous tumorigenic processes. This study aimed to clarify the prognostic significance of CENP-F expression in patients with esophageal squamous cell carcinoma (ESCC). The levels of CENP-F messenger RNA and protein were higher in ESCC cell lines than in the normal tissues. An immunohistochemical analysis of paired tissue specimens showed that the CENP-F expression was higher in tumorous tissues than in the adjacent non-tumorous tissues (P<0.001). Moreover, there was a significant correlation between CENP-F expression and gender (P=0.012), clinical stage (P=0.039), and T classification (P=0.026). Patients with higher CENP-F expression had shorter overall survival than those with lower CENP-F expression (P=0.009). Multivariate Cox analysis indicated that CENP-F expression is an independent prognostic factor for overall survival (hazard ratio=0.582, 95% confidence interval=0.397-0.804, P=0.041). Importantly, it was found that zoledronic acid (ZOL) could significantly enhance the chemotherapeutic sensitivity of ESCC cell lines with high CENP-F expression to cisplatin, although ZOL alone only exhibited a minor inhibitory effect to ESCC cells. In summary, these findings demonstrate that CENP-F may serve as a valuable molecular marker for predicting the prognosis of ESCC patients. In addition, the data indicate a potential benefit of combining ZOL with cisplatin in ESCC, suggesting that CENP-F expression may have therapeutic implications. © 2012 the Authors © 2012, Wiley Periodicals, Inc. and the International Society for Diseases of the Esophagus.

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Mi, Y. J., Gao, J., Xie, J. D., Cao, J. Y., Cui, S. X., Gao, H. J., … Chen, Y. Q. (2013). Prognostic relevance and therapeutic implications of centromere protein F expression in patients with esophageal squamous cell carcinoma. Diseases of the Esophagus, 26(6), 636–643. https://doi.org/10.1111/dote.12002

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