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The activation of adenosine monophosphate-activated protein kinase inhibits the migration of tongue squamous cell carcinoma cells by targeting Claudin-1 via epithelial-mesenchymal transition.
Zhou, Xin-Yue; Liu, Qiu-Ming; Li, Zhuang; Liu, Xia-Yang; Zhao, Qi-Wei; Wang, Yu; Wu, Feng-Hua; Zhao, Gang; Sun, Rui; Guo, Xiao-Hong.
Afiliación
  • Zhou XY; Department of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Liu QM; Hubei Shizhen Laboratory, Wuhan, Hubei, China.
  • Li Z; Sino-German Biomedical Center, Hubei University of Technology, Wuhan, China.
  • Liu XY; Center of Applied Biotechnology, Wuhan Institute of Bioengineering, Wuhan, China.
  • Zhao QW; Department of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Wang Y; Department of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Wu FH; Department of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Zhao G; Department of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Sun R; Department of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Guo XH; Hubei Shizhen Laboratory, Wuhan, Hubei, China.
Animal Model Exp Med ; 2024 Jul 17.
Article en En | MEDLINE | ID: mdl-39017036
ABSTRACT

BACKGROUND:

The role of Claudin-1 in tongue squamous cell carcinoma (TSCC) metastasis needs further clarification, particularly its impact on cell migration. Herein, our study aims to investigate the role of Claudin-1 in TSCC cell migration and its underlying mechanisms.

METHODS:

36 TSCC tissue samples underwent immunohistochemical staining for Claudin-1. Western blotting and immunofluorescence analyses were conducted to evaluate Claudin-1 expression and distribution in TSCC cells. Claudin-1 knockdown cell lines were established using short hairpin RNA transfection. Migration effects were assessed through wound healing assays. Furthermore, the expression of EMT-associated molecules was measured via western blotting.

RESULTS:

Claudin-1 expression decreased as TSCC malignancy increased. Adenosine monophosphate-activated protein kinase (AMPK) activation led to increased Claudin-1 expression and membrane translocation, inhibiting TSCC cell migration and epithelial-mesenchymal transition (EMT). Conversely, Claudin-1 knockdown reversed these inhibitory effects on migration and EMT caused by AMPK activation.

CONCLUSIONS:

Our results indicated that AMPK activation suppresses TSCC cell migration by targeting Claudin-1 and EMT pathways.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Animal Model Exp Med Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Animal Model Exp Med Año: 2024 Tipo del documento: Article País de afiliación: China
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