Downregulation of survivin expression and elevation of caspase-3 activity involved in pitavastatin-induced HepG 2 cell apoptosis

被引:10
作者
Wang, Juyong [1 ]
Xu, Zhenye [1 ]
Zhang, Ming [1 ]
机构
[1] Shanghai Acad Tradit Chinese Med, Tumor Res Inst, Shanghai 200032, Peoples R China
关键词
apoptosis; survivin; caspase-3; hepatocellular carcinoma cell; pitavastatin;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of the present study was to research the apoptosis of human hepatocellular carcinoma cell line HepG 2 induced by pitavastatin. HepG 2 cells were treated with increasing doses of pitavastatin or with mevalonic acid for 48 h. The proliferation of cells was detected with WST-8. The morphology of the nucleus was observed under a microscope by Hoechst 33258 staining. The apoptosis peaks were examined by flow cytometry. The expression of survivin mRNA was examined with RT-PCR. The caspase-3 activity was detected with caspase-3 colorimetric protease assay. We found that growth inhibitory effects were observed for treatment with pitavastatin at 10-50 mu M. Pitavastatin at 10 mu M induced granular apoptotic bodies of HepG 2 cells. Furthermore, pitavastatin at 10 mu M increased the appearance of sub-G1 population of HepG 2 cells. Finally, pitavastatin at 10 mu M downregulated the expression of survivin mRNA and upregulated the caspase-3 activity, which was clearly related to the HMG-CoA reductase activity. These results suggest that pitavastatin at 10 mu M induces apoptosis of HepG 2 cells, which is associated with the decreased expression of survivin mRNA and increased caspase-3 activity of HepG 2 cells.
引用
收藏
页码:383 / 387
页数:5
相关论文
共 32 条
[1]  
Bao Shi-Ting, 2006, Hepatobiliary Pancreat Dis Int, V5, P580
[2]   A key role for caspase-2 and caspase-3 in the apoptosis induced by 2-chloro-2′-deoxy-adenosine (Cladribine) and 2-chloro-adenosine in human astrocytoma cells [J].
Ceruti, S ;
Beltrami, E ;
Matarrese, P ;
Mazzola, A ;
Cattabeni, F ;
Malorni, W ;
Abbracchio, MP .
MOLECULAR PHARMACOLOGY, 2003, 63 (06) :1437-1447
[3]  
Chan KKW, 2003, CLIN CANCER RES, V9, P10
[4]  
Chen TA, 2003, CANCER RES, V63, P4368
[5]   Emodin induces apoptosis in human promyeloleukemic HL-60 cells accompanied by activation of caspase 3 cascade but independent of reactive oxygen species production [J].
Chen, YC ;
Shen, SC ;
Lee, WR ;
Hsu, FL ;
Lin, HY ;
Ko, CH ;
Tseng, SW .
BIOCHEMICAL PHARMACOLOGY, 2002, 64 (12) :1713-1724
[6]  
Chiou SK, 2003, MED SCI MONITOR, V9, P125
[7]   Use of siRNAs and antisense oligonucleotides against survivin RNA to inhibit steps leading to tumor angiogenesis [J].
Coma, S ;
Noe, V ;
Lavarino, C ;
Adán, J ;
Rivas, M ;
López-Matas, M ;
Pagan, R ;
Mitjans, F ;
Vilaró, S ;
Piulats, J ;
Ciudad, CJ .
OLIGONUCLEOTIDES, 2004, 14 (02) :100-113
[8]   Cerivastatin, an inhibitor of HMG-CoA reductase, inhibits the signaling pathways involved in the invasiveness and metastatic properties of highly invasive breast cancer cell lines:: an in vitro study [J].
Denoyelle, C ;
Vasse, M ;
Körner, M ;
Mishal, Z ;
Ganné, F ;
Vannier, JP ;
Soria, J ;
Soria, C .
CARCINOGENESIS, 2001, 22 (08) :1139-1148
[9]   Down-regulation of caspase 3 in breast cancer: a possible mechanism for chemoresistance [J].
Devarajan, E ;
Sahin, AA ;
Chen, JS ;
Krishnamurthy, RR ;
Aggarwal, N ;
Brun, AM ;
Sapino, A ;
Zhang, F ;
Sharma, D ;
Yang, XH ;
Tora, AD ;
Mehta, K .
ONCOGENE, 2002, 21 (57) :8843-8851
[10]  
FERNANDESALNEMRI T, 1994, J BIOL CHEM, V269, P30761