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P-cadherin promotes cervical cancer growth and invasion through affecting the expression of E-cadherin and p120 catenin
1Department of Gynecologic Oncology, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China
DOI: 10.12892/ejgo4374.2019 Vol.40,Issue 2,April 2019 pp.224-231
Accepted: 03 August 2017
Published: 10 April 2019
*Corresponding Author(s): Xiaoyun Wan E-mail: wanxy@zju.edu.cn
Objective: The aim of the present study was to investigate the role of P-cadherin in cervical carcinogenesis and cancer progression. Materials and Methods: The expression of placental cadherin (P-cadherin) protein was examined by Western blot in different cervical samples and cervical cell lines. Through regulating P-cadherin expression in Siha or 293T cells, cell growth, migration, and invasion were examined separately using a cell-counting kit-8 (CCK-8) or Transwell assays, and meanwhile the expression of cadherin/catenin complex was tested using Western blot. Results: Western blot showed that P-cadherin was overexpressed in cervical cancer tissues and cancer-derived cell lines compared with normal cervical tissues. Silencing P-cadherin expression resulted in increase of epithelial cadherin (E-cadherin) and decrease of p120 catenin (p120ctn) expression, which was accompanied by inhibiting cell growth and reducing cell migration and invasion. Conversely, overexpression of P-cadherin led to downregulation of E-cadherin and upregulation of p120ctn expression, which was accompanied by promoting cell growth and increasing cell migration and invasion. Conclusions: P-cadherin could promote cervical cancer growth and invasion, at least partly through affecting the expression of E-cadherin and p120 catenin, consequently contributing to cervical carcinogenesis and cancer progression.
P-cadherin; E-cadherin; p120ctn; Metastasis; Cervical cancer
Baohua Li,Danzhu Gong,Fenfen Wang,Xiaoyun Wan. P-cadherin promotes cervical cancer growth and invasion through affecting the expression of E-cadherin and p120 catenin. European Journal of Gynaecological Oncology. 2019. 40(2);224-231.
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