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Perifosine as potential anti-cancer agent inhibits proliferation, migration, and tube formation of human umbilical vein endothelial cells.
Wang, Feng Ze; Fei, Hong Rong; Li, Xiao Qian; Shi, Renjiu; Wang, De Cai.
Afiliación
  • Wang FZ; School of Biological Science, Taishan Medical University, Taian 271016, People's Republic of China. fengzewang@gmail.com
Mol Cell Biochem ; 368(1-2): 1-8, 2012 Sep.
Article en En | MEDLINE | ID: mdl-21769450
Targeting angiogenesis is considered an effective strategy for treating the expansion and metastasis of tumors. The aim of this study is to assess the effects of perifosine, an inhibitor of Akt, on cell proliferation, apoptosis, angiogenesis, and VEGF-induced cell migration in cultured human umbilical vein endothelial cells (HUVECs) in vitro. MTT and cell cycle analysis results indicated that perifosine inhibited the growth of HUVECs in a dose-dependent manner, arrested cell cycle progression at the G(2) phase with regulation the expression of p21 and cyclinB1. Apoptosis induced by the higher concentrations of perifosine in HUVECs was also observed. In addition, tube formation of HUVECs and VEGF-induced cell migration were markedly inhibited by perifosine. Western blotting analysis of cell signaling molecules indicated that perifosine inhibited ERK and p38 phosphorylation in HUVECs. These results suggest that perifosine exerts anti-angiogenic activity in HUVECs and is a promising agent for treatment of angiogenesis related-diseases.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fosforilcolina / Movimiento Celular / Fase G2 / Células Endoteliales de la Vena Umbilical Humana / Neovascularización Patológica / Antineoplásicos Límite: Humans Idioma: En Revista: Mol Cell Biochem Año: 2012 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fosforilcolina / Movimiento Celular / Fase G2 / Células Endoteliales de la Vena Umbilical Humana / Neovascularización Patológica / Antineoplásicos Límite: Humans Idioma: En Revista: Mol Cell Biochem Año: 2012 Tipo del documento: Article Pais de publicación: Países Bajos