Volume 57, Issue 7 pp. 896-902
RESEARCH ARTICLE

Oleanolic acid induces osteosarcoma cell apoptosis by inhibition of Notch signaling

Ying Xu

Ying Xu

Department of Anesthesiology, Shengjing Hospital, China Medical University, Shenyang, P.R. China

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Bing Shu

Bing Shu

Longhua Hospital and Spine Disease Research Institute, Shanghai University of Traditional Chinese Medicine, Shanghai, P.R. China

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Ye Tian

Corresponding Author

Ye Tian

Department of Orthopaedic Surgery, Shengjing Hospital, China Medical University, Shenyang, P.R. China

Correspondence

Ye Tian, MD, PhD, Department of Orthopaedic Surgery, Shengjing Hospital, China Medical University, Shenyang, P.R. China.

Email: [email protected]

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Guangxi Wang

Guangxi Wang

Department of Orthopaedic Surgery, Louisiana State University Health Sciences Center, Shreveport, Lousiana

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Yongjun Wang

Yongjun Wang

Longhua Hospital and Spine Disease Research Institute, Shanghai University of Traditional Chinese Medicine, Shanghai, P.R. China

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Jinwu Wang

Jinwu Wang

Department of Orthopaedic Surgery, Shanghai Ninth people's Hospital, Shanghai, P.R. China

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Yufeng Dong

Yufeng Dong

Longhua Hospital and Spine Disease Research Institute, Shanghai University of Traditional Chinese Medicine, Shanghai, P.R. China

Department of Orthopaedic Surgery, Louisiana State University Health Sciences Center, Shreveport, Lousiana

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First published: 22 March 2018
Citations: 26

Abstract

Oleanolic acid (OA), a naturally occurring triterpenoid, exhibits potential antitumor activity in several tumor cell lines. Although the inhibition effects of OA on proliferation and survival in human cancers have been confirmed, the potential mechanism underlying OA-induced osteosarcoma cell death has not yet been fully elucidated. Our results in this study showed that OA inhibits proliferation and viability of osteosarcoma cells in a dose-dependent manner. Flow cytometry assays revealed that apoptosis in osteosarcoma cells was significantly induced by OA treatment, while this induction was blocked by Jagged1-mediated activation of Notch signaling. Western blot analysis and a mitochondrial membrane potential assay demonstrated that OA functions through the mitochondrial apoptosis pathway. More importantly, our data revealed that OA treatment interrupted the balance between pro-apoptotic factors and anti-apoptotic factors in osteosarcoma cells by inhibition of the Notch signaling pathway. These data suggest that OA induces osteosarcoma cell apoptosis by targeting mitochondria in a Notch signaling-dependent manner. Thus, OA may be a promising drug for adjuvant chemotherapy in osteosarcoma.

CONFLICTS OF INTEREST

The authors declare that there is no potential conflicts of interest.

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