Antitumor effects of baicalin on ovarian cancer cells through induction of cell apoptosis and inhibition of cell migration in vitro.
Antitumor effects of baicalin on ovarian cancer cells through induction of cell apoptosis and inhibition of cell migration in vitro.
复制标题
黄芩苷通过诱导细胞凋亡和抑制细胞迁移对卵巢癌细胞的体外抗肿瘤作用
DOI:
10.3892/mmr.2017.7757
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发表时间:
2017-12
影响因子:
3.4
通讯作者:
Tian W
中科院分区:
文献类型:
--
作者:
Gao C;Zhou Y;Li H;Cong X;Jiang Z;Wang X;Cao R;Tian W
Baicalin, an active flavone isolated from Scutellaria baicalensis Georgi, has been demonstrated to induce various beneficial biochemical effects such as anti-inflammatory, anti-viral, and antitumor effects. However, the antitumor mechanism of baicalin is not well understood. In the present study, baicalin was demonstrated to inhibit the viability and migration of a widely used ovarian cancer cell line, A2780, in a dose-dependent manner. MTT assays revealed that cell viability significantly decreased in ovarian cancer cells treated with baicalin compared with untreated cells, without effect on normal ovarian cells. Flow cytometric analysis indicated that baicalin suppressed cell proliferation by inducing apoptosis. The underlying mechanisms involved were indicated to be downregulation of the anti-apoptotic protein B-cell lymphoma 2 apoptosis regulator and activation of caspase-3 and −9. In addition, wound healing and transwell assays revealed that cell migratory potential and expression of matrix metallopeptidase (MMP)-2 and MMP-9 were significantly inhibited when cells were exposed to baicalin, compared with untreated cells. The present study therefore suggested that baicalin has the potential to be used in novel anti-cancer therapeutic formulations for treatment of ovarian cancer.
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影响因子:
7.2
作者:
Wang, Congpin;Wang, Bin
通讯作者:
Wang, Bin
影响因子:
3.2
作者:
Ye, Chun;Li, Sali;Hou, Yongqing
通讯作者:
Hou, Yongqing
影响因子:
2.9
作者:
Fujiwara Y;Takaishi K;Nakao J;Ikeda T;Katabuchi H;Takeya M;Komohara Y
通讯作者:
Komohara Y
影响因子:
3.4
作者:
Kim, Min Kyoung;Choi, Hyeong Sim;Ko, Seong-Gyu
通讯作者:
Ko, Seong-Gyu
影响因子:
1.8
作者:
Ahmed, Khadija Muhamed
通讯作者:
Ahmed, Khadija Muhamed