BW18, a C-21 steroidal glycoside, exerts an excellent anti-leukemia activity through inducing S phase cell cycle arrest and apoptosis via MAPK pathway in K562 cells

被引:25
作者
Yang, Jue [1 ,2 ,3 ]
Chen, Li [4 ]
Yan, Ying [1 ,2 ,3 ]
Qiu, Jianfei [1 ,2 ,3 ]
Chen, Juan [1 ,2 ,3 ]
Song, Jingrui [1 ,2 ,3 ]
Rao, Qing [1 ,2 ,3 ]
Ben-David, Yaacov [1 ,2 ,3 ]
Li, Yanmei [1 ,2 ,3 ]
Hao, Xiaojiang [1 ,2 ,3 ]
机构
[1] Guizhou Med Univ, State Key Lab Funct & Applicat Med Plants, Guiyang 550014, Guizhou, Peoples R China
[2] Key Lab Chem Nat Prod Guizhou Prov, Guiyang 550014, Guizhou, Peoples R China
[3] Chinese Acad Sci, Guiyang 550014, Guizhou, Peoples R China
[4] Guiyang Univ Chinese Med, Guiyang 550025, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Chronic myeloid leukemia; BW18; Cell cycle arrest; Cell apoptosis; MAPK pathway; P38; MAPK; SIGNALING PATHWAYS; CYNANCHUM-ATRATUM; GROWTH-INHIBITION; NATURAL-PRODUCT; CANCER-CELLS; LEUKEMIA; DIFFERENTIATION; ROLES; BCR;
D O I
10.1016/j.biopha.2019.108603
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
C-21 steroids displayed the activities of immunosuppressive, anti-inflammatory and anti-virus effects by the reports. However, its antitumor effects and molecular mechanism remain unclear. We previously isolated and identified a C-21 steroidal glycoside (BW18) from the root of Cynanchum atratum Bunge. This study was aimed to assess anti-leukemia activity and its underlying mechanism in K562 cells. MTT assay results showed that BW18 inhibited cell viability and proliferation of K562 cells. We also found that BW18 could induce S phase cell cycle arrest and apoptosis. Furthermore, our results demonstrated that BW18 regulated the expression of apoptosis and cell cycle related proteins. Mechanism investigation revealed that the anti-leukemia activity of BW18 may be mediated through MAPK pathway. These findings indicate that BW18 possesses an excellent anti-leukemia activity via regulating MAPK pathway leading to S phase cell cycle arrest and apoptosis, which suggested BW18 could be as a potential alternative therapeutic agent for CML patients.
引用
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页数:7
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