Apoptosis induction of oroxylin A in human cervical cancer HeLa cell line in vitro and in vivo

被引:95
|
作者
Li, Hua-Nan [2 ]
Nie, Fei-Fei [1 ]
Liu, Wei [1 ]
Dai, Qin-Sheng [1 ]
Lu, Na [1 ]
Qi, Qi [1 ]
Li, Zhi-Yu [1 ]
You, Qi-Dong [1 ]
Guo, Qing-Long [1 ,3 ]
机构
[1] China Pharmaceut Univ, Jiangsu Key Lab Carcinogenesis & Intervent, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Nanjing 210009, Peoples R China
[3] Jiangsu Ctr Pharmacodynam Res & Evaluat, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金;
关键词
Oroxylin A; Apoptosis; Caspase; Nude mice; HeLa cells; ANTITUMOR-ACTIVITY; KAPPA-B; PROLIFERATION; INHIBITION; ACTIVATION; EXPRESSION; GENISTEIN; CHANNEL; DEATH; MODEL;
D O I
10.1016/j.tox.2008.12.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oroxylin A is a flavonoid that is found in the roots of Scutellaria baicalensis Georgi. Here. we investigated the antitumor effect of oroxylin A in human cervical cancer HeLa cell line in vitro and in vivo. We found that after inoculated with the HeLa cells the mice treated with oroxylin A showed a significant decrease of tumor volumes and tumor weight compared with the control. Meanwhile, the growth inhibition of oroxylin A on HeLa cells were observed by MTT assay and the value of IC50 was 19.4 +/- 0.7 mu M after treatment for 48 h. Upon our previous research, the inhibition by oroxylin A might be through apoptosis. Then apoptosis induced by oroxylin A in HeLa cells was characterized by DAPI staining and Annexin V/PI double staining, and degradation of PARP (poly-ADP-ribose polymerase) was both found in HeLa cells and tumor tissue. Next, activation of the caspase cascade for both the extrinsic and intrinsic pathways were demonstrated in vivo and in vitro, including caspase-8, -9 and -3. We also found that the expression of Bcl-2 protein decreased, which leading to an increase of the Bax/Bcl-2 ratio. Our results showed that oroxylin A exhibited strong antitumor effect in HeLa cell line and apoptosis induction involved in it. (c) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:80 / 85
页数:6
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