CEP55 Positively Affects Tumorigenesis of Esophageal Squamous Cell Carcinoma and Is Correlated with Poor Prognosis

Author:

Yan Shu-Mei12ORCID,Liu Lili12,Gu Wan-Yi3,Huang Li-Yun12,Yang Yi4,Huang Yu-Hua12ORCID,Luo Rong-Zhen12ORCID

Affiliation:

1. Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, China

2. Department of Pathology, Sun Yat-Sen University Cancer Center, Guangzhou, China

3. Department of Pathology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

4. Boao Evergrande International Hospital, Hainan, China

Abstract

Centrosomal protein 55 (CEP55) is a centrosome- and midbody-associated protein that is overexpressed in several cancers. However, the underlying molecular mechanism of CEP55-mediated progression and metastasis of esophageal squamous cell carcinoma (ESCC) is not clear. In the current study, we detected CEP55 mRNA by qRT-PCR while protein expression was detected by western blot analysis and immunohistochemistry (IHC). In addition, we knocked down CEP55 and investigated the ability of CEP55 to affect colony formation and migration. Here, we report that CEP55 mRNA and protein expression was significantly increased in ESCC. IHC staining showed that CEP55 expression correlated with TNM stage ( p = 0.046 ) and lymph node metastases ( p = 0.024 ). According to overall survival (OS) and disease-free survival (DFS), patients whose tumors expressed a higher level of CEP55 had a poorer prognosis than those with low expression level of CEP55. A multivariate analysis revealed that CEP55 expression was an independent prognostic indicator for patients with ESCC. Knockdown of CEP55 decreased the colony formation ability and migration of ESCC cells and also reduced the phosphorylation of Src, FAK, and ERK. Therefore, our study implied that CEP55 may be a valuable biomarker and a potential target in the treatment of patients with ESCC.

Funder

Guangdong Medical Science and Technology Research Fund

Publisher

Hindawi Limited

Subject

Oncology

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