The anti-tumor effect of pachymic acid on osteosarcoma cells by inducing PTEN and Caspase 3/7-dependent apoptosis

被引:43
作者
Wen, Huilong [1 ,3 ]
Wu, Zhong [2 ]
Hu, Huidong [1 ]
Wu, Yixiong [1 ]
Yang, Gang [1 ]
Lu, Jiajun [1 ]
Yang, Guang [3 ]
Guo, Gang [4 ]
Dong, Qirong [3 ]
机构
[1] Suzhou Univ, Dept Orthoped, Changzhou Tumor Hosp, Changzhou 213000, Peoples R China
[2] Tongji Univ, Sch Med, Dept Orthoped, Shanghai Peoples Hosp 10, Shanghai 200072, Peoples R China
[3] Soochow Univ, Dept Orthoped, Affiliated Hosp 2, Suzhou 215004, Jiangsu, Peoples R China
[4] Tongji Univ, Tongji Hosp, Dept Emergency, Sch Med, Shanghai 200065, Peoples R China
关键词
Pachymic acid; Osteosarcoma; PTEN; Caspase; 3; Apoptosis; PORIA-COCOS; TUMOR-SUPPRESSOR; UP-REGULATION; CANCER CELLS; ACTIVATION; PATHWAYS; THERAPY; GROWTH; ROLES; AKT;
D O I
10.1007/s11418-017-1117-2
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pachymic acid (PA) is a lanostane type triterpenoid isolated from Poria cocos, which possesses an anti-tumor effect in breast cancer, prostate cancer, lung cancer, and bladder cancer cells. In this study, we investigated the effect of PA on the growth and apoptosis of human immortalized cell line (HOS) and primary osteosarcoma cells by a Cell Counting Kit-8 (CCK-8) and Annexin V and propidium iodide (PI) staining, respectively. Western blot was used to measure the expression of cleaved Caspase 3, PTEN, and AKT, as well as the AKT phosphorylation. The Caspase 3 activity was determined using the Caspase-3 Colorimetric Assay Kit. From the results, PA significantly reduced cell proliferation in a concentration- and time-dependent manner. PA also induced cell apoptosis in a dose-dependent fashion. PA treatment led to increased Caspase 3 activation and PTEN expression, as well as reduced AKT phosphorylation. Moreover, Ac-DEVD-CHO (a Caspase 3/7 inhibitor) pre-treatment or PTEN knockdown partially blocked the effects of PA on cell proliferation and apoptosis. Caspase 3/7 inhibitor had an additive effect with PTEN knockdown. Collectively, our results suggested that induction of apoptosis by PA was mediated in part by PTEN/AKT signaling and Caspase 3/7 activity. This study provides evidence that PA might be useful in the treatment of human osteosarcoma.
引用
收藏
页码:57 / 63
页数:7
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