GENISTEIN INHIBITS PROLIFERATION OF HUMAN ENDOMETRIAL ENDOTHELIAL CELL IN VITRO

被引:8
作者
Guihua Sha and Shouqing Lin Gynecological Endocrinology LaboratoryDepartment of Obstetrics and GynecologyPeking Union Medical College HospitalChinese Academy of Medical Sciences Peking Union Medical CollegeBeijing [100730 ]
机构
关键词
genistein; angiogenesis; human endometrial endothelial cell; human endometrialcancer-1B cell; proliferation;
D O I
暂无
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective To explore the effect of genistein on proliferation of human endometrial endothelial cells(HEECs)and glandular epithelium.Methods In vitro HEECs and human endometrial cancer-1B cell(HEC-1B)were cultured with 0,1,10,50,100,and 200 μmol/L of genistein alone or indicated concentrations of genistein combined with 0.2 or 1 nmol/L 17β-estradiol(17β-E2).Cell proliferation was determined by[3H]-thymidine incorporation and cell cycle was measured by flow cytometry.Results After 96 hours of treatment,genistein inhibited the proliferation of HEECs in a dose-dependent manner.The stimulation index reduced from 100%(without genistein treatment)to about 1%(200 μmol/L genistein).HEECs were arrested at G1/0 and G2/M phase when treated with genistein for 96 hours.When the concentration of genistein was 200 μmol/L,the percentages of HEECs at G1/0,G2/M,and S phase were 96.0%,2.1%,and 1.9%,respectively.However,when HEECs were treated without genistein,the percentages of HEECs at G1/0,G2/M,and S phase were 76.7%,8.5%,and 14.7%,respectively.17β-E2 could not influence the effects of genistein on the proliferation of HEECs.Meanwhile,genistein could suppress the proliferation of HEC-1B.If the stimulation index of HEC-1B was defined as 100% when HEC-1B was treated with different doses of 17β-E2(without genistein),it was 67%,19%,as well as 32% when cell was supplemented with 200 μmol/L genistein combined with 0,0.2,or 1 nmol/L 17β-E2,respectively.Conclusion Genistein at the concentration of 200 μmol/L can sufficiently inhibit the proliferation of HEECs and endometrial glandular epithelium simultaneously in vitro.
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页码:49 / 53
页数:5
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