Crude Extract of Rheum palmatum L. Induces Cell Cycle Arrest S Phase and Apoptosis Through Mitochondrial-Dependent Pathways in U-2 OS Human Osteosarcoma Cells

被引:12
作者
Lin, Chin-Chung [1 ,2 ]
Lee, Ming-Huei [2 ,3 ]
Lin, Ju-Hwa [4 ]
Lin, Meng-Liang [5 ]
Chueh, Fu-Shin [6 ]
Yu, Chien-Chih [7 ]
Lin, Jing-Pin [8 ]
Chou, Yu-Cheng [9 ,10 ]
Hsu, Shu-Chun [4 ]
Chung, Jing-Gung [4 ,11 ]
机构
[1] Feng Yuan Hosp, Dept Chinese Med, Minist Hlth & Welf, Taichung 420, Taiwan
[2] Cent Taiwan Univ Sci & Technol, Gen Educ Ctr, Taichung 406, Taiwan
[3] Feng Yuan Hosp, Dept Urol, Minist Hlth & Welf, Taichung 420, Taiwan
[4] China Med Univ, Dept Biol Sci & Technol, Taichung 404, Taiwan
[5] China Med Univ, Dept Med Lab Sci & Biotechnol, Taichung, Taiwan
[6] Asia Univ, Dept Hlth & Nutr Biotechnol, Taichung 413, Taiwan
[7] China Med Univ, Sch Pharm, Taichung 404, Taiwan
[8] China Med Univ, Sch Chinese Med, Taichung 404, Taiwan
[9] Taichung Vet Gen Hosp, Neurol Inst, Div Neurosurg Oncol, Taichung 407, Taiwan
[10] Tzu Chi Univ, Inst Med Sci, Hualien 970, Taiwan
[11] Asia Univ, Dept Biotechnol, Taichung 413, Taiwan
关键词
crude extract of Rheum palmatum L. (CERP); human osteosarcoma cells U-2 OS; cell cycle arrest; apoptosis; CARCINOMA-CELLS; CANCER-CELLS; UP-REGULATION; IN-VITRO; INDUCTION; DEATH; ACTIVATION; EXPRESSION; DYSFUNCTION; INHIBITION;
D O I
10.1002/tox.22105
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Cancer is the second cause of death in children. Osteosarcoma is the most common primary malignancy of solid bone cancer primarily affecting adolescents and young adults. In the Chinese population, the crude extract of Rheum palmatum L. (CERP) has been used for treating different diseases, including SARS, rheumatoid arthritis, coxsackievirus B3, and human colon cancer cell, pancreatic cancer. There are no reports on CERP and human osteosarcoma cells. The present study examined effects of CERP on cytotoxicity including cell cycle distribution and cell death (apoptosis) in U-2 OS human osteosarcoma cells. CERP significantly induced S phase arrest in U-2 OS cells in a dose-dependent. CERP produced DNA damage and DNA condensation. Other effects of CERP were stimulation of ROS and Ca2+, mitochondria impairment, and activation of caspase -3, -8, and -9. CERP increased the levels of Bax, Bak, Bad, cyclin B, Fas, PARP, GRP78, GADD153, AIF, Endo G, Calpain-2, p21, and p27, but decreased the levels of Bcl-2, BCL-X, XIAP, Akt, CDC25A, CDK2, Cyclin A, and Cyclin E of U-2 OS cells. It was also observed that CERP promoted the expression of AIF, Endo G, GADD153, and cytochrome c. These results indicate that CERP has anticancer effects in vitro and provide the foundation for in vivo studies of animal models of osteosarcoma. (C) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:957 / 969
页数:13
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