Apigenin inhibits cell migration through MAPK pathways in human bladder smooth muscle cells
Biocell
;
35(3): 71-79, Dec. 2011. tab
Artículo
en Inglés
| LILACS
| ID: lil-653213
ABSTRACT
Apigenin, a nonmutagenic flavonoid, has been shown to possess free radical scavenging activities, anticarcinogenic properties, antioxidant and anti-inflammatory effects. Recently, apigenin was reported to cause gastric relaxation in murine. To assess possible effects of apigenin on migration of bladder smooth muscle (SM) cell, we isolated SM cells from peri-cancer tissue of human bladder and established a cell model that was capable to overexpress transiently MEKK1 (MEK kinase 1). Results showed that overexpression of active human MEKK1 by adenoviruses infection induced migration of human bladder smooth muscle (hBSM) cells and phosphorylation of MAPKs, ERK, JNK and p38, which are the downstream molecules of MEKK1. Then, hBSM cell overexpressing MEKK1 were exposed to apigenin (50 microM). Our data indicated that apigenin inhibited significantly activation/phosphorylation of MAPKs and migration of hBSM cells induced by MEKK1 overexpression. Besides, apigenin inhibited actin polymerization, which underlines muscle contraction and cell migration. The results suggest that apigenin inhibits activation of MAPKs and thereby the cell migration. The mechanism might be that apigenin blocks signal transmission from MEKK1 to MAPKs.
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Índice:
LILACS (Américas)
Asunto principal:
Flavonoides
/
Vejiga Urinaria
/
Movimiento Celular
/
Miocitos del Músculo Liso
/
Apigenina
/
Quinasa 1 de Quinasa de Quinasa MAP
Límite:
Animales
/
Humanos
Idioma:
Inglés
Revista:
Biocell
Asunto de la revista:
Clulas
Año:
2011
Tipo del documento:
Artículo
País de afiliación:
China
Institución/País de afiliación:
Jiangsu Polytechnic College of Agriculture and Forestry/CN
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