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PZR promotes metastasis of colorectal cancer through increasing FAK and Src phosphorylation.
Tan, Dan; Zhang, Wenpeng; Tao, Yu; Galiya, Yesseyeva; Wang, Mingliang.
Afiliación
  • Tan D; Department of General Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Zhang W; Department of General Surgery, Ruijin Hospital Luwan Branch, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Tao Y; Department of General Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Galiya Y; Department of General Surgery, Ruijin Hospital Luwan Branch, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Wang M; The Key Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Jiao Tong University School of Medicine and Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Acta Biochim Biophys Sin (Shanghai) ; 51(4): 356-364, 2019 Apr 01.
Article en En | MEDLINE | ID: mdl-30877754
ABSTRACT
Metastasis is the main cause of death in patients with colorectal cancer (CRC), but the molecular mechanism is not yet fully understood. Previous studies have shown that P zero-related protein (PZR), a member of the immunoglobulin family, can promote fibronectin-dependent migration of mouse embryonic fibroblasts as well as invasion and metastasis of hepatic carcinoma cells. However, the role of PZR in CRC remains unclear. In this study, we determined the ectopic expression of PZR in CRC tissues, and results showed that PZR expression was increased not only in tumors with higher pathological stage, but also in tumors with distant metastasis. Through PZR-knockdown and overexpression in CRC cell lines, we found that the expression of PZR had significant effect on the invasion and migration of CRC cells as well as the phosphorylation of pro-metastasis proteins including focal adhesion kinase (FAK) and Src. Taken together, this study indicates that PZR may promote the invasion and migration of CRC cells through increasing the phosphorylation of FAK and Src, which provides a new theoretical basis and a possible marker for the diagnosis or prognosis of CRC metastasis.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fosfoproteínas / Neoplasias Colorrectales / Familia-src Quinasas / Péptidos y Proteínas de Señalización Intracelular / Proteína-Tirosina Quinasas de Adhesión Focal Tipo de estudio: Prognostic_studies Idioma: En Revista: Acta Biochim Biophys Sin (Shanghai) Asunto de la revista: BIOFISICA / BIOQUIMICA Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fosfoproteínas / Neoplasias Colorrectales / Familia-src Quinasas / Péptidos y Proteínas de Señalización Intracelular / Proteína-Tirosina Quinasas de Adhesión Focal Tipo de estudio: Prognostic_studies Idioma: En Revista: Acta Biochim Biophys Sin (Shanghai) Asunto de la revista: BIOFISICA / BIOQUIMICA Año: 2019 Tipo del documento: Article