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The anti-tumor effect of pachymic acid on osteosarcoma cells by inducing PTEN and Caspase 3/7-dependent apoptosis
Authors:Huilong Wen  Zhong Wu  Huidong Hu  Yixiong Wu  Gang Yang  Jiajun Lu  Guang Yang  Gang Guo  Qirong Dong
Affiliation:1.Department of Orthopedics,Changzhou Tumor Hospital Affiliated to Suzhou University,Changzhou,People’s Republic of China;2.Department of Orthopedics, Shanghai Tenth People’s Hospital,Tongji University School of Medicine,Shanghai,People’s Republic of China;3.Department of Orthopedics,The Second Affiliated Hospital of Soochow University,Suzhou,People’s Republic of China;4.Department of Emergency, Tongji Hospital,Tongji University School of Medicine,Shanghai,People’s Republic of China
Abstract:
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.
Keywords:
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