Genistein inhibits glioma cell proliferation and suppresses gD gene expression in HSV-1 infection

被引:0
作者
Wang, Qian [1 ]
Cui, Jian [2 ]
Wang, Bin [1 ]
Wang, Haibo [2 ]
Li, Ling [1 ]
机构
[1] Qingdao Univ, Coll Med, Dept Microbiol, Ningxia Rd 308, Qingdao 266071, Shandong, Peoples R China
[2] Qingdao Univ, Affiliated Hosp, Breast Ctr, Qingdao 266071, Shandong, Peoples R China
关键词
Genistein; HSV-1; U251; proliferation; apoptosis; VIRUS TYPE-1 INFECTION; IN-VITRO; ANTIVIRAL ACTIVITY; SOY ISOFLAVONES; BREAST-CANCER; GROWTH-FACTOR; P38; MAPK; KINASE; PROTEIN;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This study aims to investigate inhibitory effects of Genistein (GST) on abnormal changes of proliferation and apoptosis in Human Glioma cell (U251) induced by HSV-1. U251 cells were infected by HSV-1 at a multiplicity of infection of 5. GST, GST+HSV-1, HSV-1 and control group were set up. MTT assay, cell apoptosis and RT-PCR were performed to detect inhibitory effects of GST on abnormal changes of proliferation and apoptosis induced by HSV-1 in U251 cells. There were great differences among different groups (P<0.05). Compared to control group, cell proliferation were inhibited in 30 mu g/ml GST and HSV-1 group (P<0.05). MTT values in 15 mu g/ml GST+HSV-1 were higher than those in HSV-1 group (P<0.05). Cell proliferation were inhibited in both 3.75 mu g/ml GST+HSV-1 and 30 mu g/ml GST+HSV-1 group compared to HSV-1 group (P<0.05). In HSV-1 group, cells started to merge at 12 h post-infection, and cytopathic effects (CPE) were observed at 36 h post-infection. In 15 mu g/ml GST+HSV-1 group, a few merges appeared at 24 h post-infection and increased at 36 h post-infection when most cells kept normal forms. Apoptosis rates in 15 mu g/ml GST+ HSV-1 group were lower than that in HSV-1 group (P<0.05). gD gene expression at 6 h post-infection in HSV-1 group and 24 h post-infection in 15 mu g/ml GST+ HSV-1 group. In conclusion, GST at appropriate concentration does not influence proliferation or apoptosis of normal cells, but could inhibit abnormality glioma cell proliferation and apoptosis, as well as gD gene expression in HSV-1 infection.
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收藏
页码:7582 / 7589
页数:8
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