화학공학소재연구정보센터
Biochemical and Biophysical Research Communications, Vol.362, No.4, 848-852, 2007
Homoisoflavanone inhibits retinal neovascularization through cell cycle arrest with decrease of cdc2 expression
Neovascularization in the eye is the most common cause of blindness in all age groups; retinopathy of prematurity (ROP), diabetic retinopathy, and age-related macular degeneration. Despite current advances in surgical treatments, ROP remains as the most serious problem of vision loss in children. Here, we report that homoisoflavanone, a natural product from Cremastra appendiculata, significantly reduces retinal neovascularization in a mouse model of ROP. Homoisoflavanone inhibited the cell growth of HUVECs, but its cytotoxic effect was not observed in a concentration range of 1-20 mu M. HUVECs population gradually increased in G(2)/M phase and reduced in G(0)/G(1) and S phases after exposure to the compound. Homoisoflavanone decreased the level of cdc2 expression whereas the level of p21(WAF1) expression was increased in a dose-dependent manner. These data demonstrate that homoisoflavanone could inhibit retinal neovascularization and be applied in the treatment of other vasoproliferative retinopathies. (c) 2007 Elsevier Inc. All rights reserved.