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PAK2 promotes proliferation, migration, and invasion of lung squamous cell carcinoma through LIMK1/cofilin signaling pathway.
Wang, Congcong; Wang, Junyan; Xu, Ruifeng; Huang, Xia; Li, Qiushuang; Zhang, Chenxi; Yuan, Baiyin.
Afiliación
  • Wang C; College of Life and Health Sciences, Wuhan University of Science and Technology, Wuhan, Hubei 430081, China.
  • Wang J; College of Life and Health Sciences, Wuhan University of Science and Technology, Wuhan, Hubei 430081, China.
  • Xu R; College of Life and Health Sciences, Wuhan University of Science and Technology, Wuhan, Hubei 430081, China.
  • Huang X; College of Life and Health Sciences, Wuhan University of Science and Technology, Wuhan, Hubei 430081, China.
  • Li Q; College of Life and Health Sciences, Wuhan University of Science and Technology, Wuhan, Hubei 430081, China.
  • Zhang C; Central Laboratory, Nanjing Chest Hospital, Affiliated Nanjing Brain Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, China.
  • Yuan B; College of Life and Health Sciences, Wuhan University of Science and Technology, Wuhan, Hubei 430081, China.
J Biomed Res ; : 1-14, 2024 May 25.
Article en En | MEDLINE | ID: mdl-38828848
ABSTRACT
Although the p21-activated kinase 2 (PAK2) is an essential serine/threonine protein kinase, its role in lung squamous cell carcinoma (LUSC) progression has yet to be fully understood. We analyzed PAK2 mRNA levels and DNA copy numbers as well as protein levels by quantitative real-time PCR and immunohistochemical staining, respectively, in human LUSC tissues and adjacent normal tissues. Then, we used colony formation assays, cell counting kit-8 assays, matrigel invasion assays, wound healing assays and xenograft models in nude mice to investigate the functions of PAK2 in LUSC progression. We demonstrated that the mRNA levels, DNA copy numbers, and protein levels of PAK2 were up-regulated in human LUSC tissues than in adjacent normal tissues. In addition, a higher PAK2 expression was correlated with a poorer prognosis in LUSC patients. In the in vitro study, we found that PAK2 promoted cell growth, migration, invasion, EMT process, and cell morphology regulation in LUSC cells. Furthermore, PAK2 enhanced tumor cell proliferation, migration, and invasion by regulating actin dynamics through the LIMK1/cofilin signaling. Our findings implicated that the PAK2/LIMK1/cofilin signaling pathway is likely a potential clinical marker and therapeutic target for LUSC.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Biomed Res Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Biomed Res Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: China