Docetaxel inhibits SMMC-7721 human hepatocellular carcinoma cells growth and induces apoptosis

被引:60
作者
Geng, CX
Zeng, ZC
Wang, JY [2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Radiat Oncol, Shanghai 200032, Peoples R China
[2] Fudan Univ, Dept Gastroenterol, Zhongshan Hosp, Shanghai 200032, Peoples R China
关键词
D O I
10.3748/wjg.v9.i4.696
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the in vitro anti-hepatocellular carcinoma (HCC) activity of docetaxel against SMMC-7721 HCC cells and its possible mechanism. METHODS: The HCC cells were given different concentrations of docetaxel and their growth was measured by colony forming assay. Cell cycle and apoptosis were analyzed by flow cytometry and fluorescence microscopy (acridine orange/ethidium bromide double staining, AO/EB), as well as electronic microscopy. The SMMC-7721 HCC cell reactive oxygen species (ROS) and glutathione (GSH) were measured after given docetaxel. RESULTS: Docetaxel inhibited the hepatocellular carcinoma cells growth in a concentration dependent manner with IC(50)5 x 10(-10) M. Marked cell apoptosis and G2/M phase arrest were observed after treatment with docetaxel greater than or equal to 10(-8) M. Docetaxel promoted SMMC-7721 HCC cells ROS generation and GSH deletion. CONCLUSION: Docetaxel suppressed the growth of SMMC-7721 HCC cells in vitro by causing apoptosis and G2/M phase arrest of the human hepatoma cells, and ROS and GSH may play a key role in the inhibition of growth and induction of apoptosis.
引用
收藏
页码:696 / 700
页数:5
相关论文
共 38 条
[1]   A phase II study of sequential chemotherapy with docetaxel after the weekly PELF regimen in advanced gastric cancer. A report from the Italian group for the study of digestive tract cancer [J].
Cascinu, S ;
Graziano, F ;
Barni, S ;
Labianca, R ;
Comella, G ;
Casaretti, R ;
Frontini, L ;
Catalano, V ;
Baldelli, AM ;
Catalano, G .
BRITISH JOURNAL OF CANCER, 2001, 84 (04) :470-474
[2]   Lymphocyte proliferation modulated by glutamine: involved in the endogenous redox reaction [J].
Chang, WK ;
Yang, KD ;
Shaio, MF .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1999, 117 (03) :482-488
[3]   Phase II study of docetaxel in patients with liver metastases from breast cancer [J].
Coleman, RE ;
Howell, A ;
Eggleton, SPH ;
Maling, SJ ;
Miles, DW .
ANNALS OF ONCOLOGY, 2000, 11 (05) :541-546
[4]  
Donnellan P, 1998, SEMIN ONCOL, V25, P20
[5]   Phase II trial of docetaxel and cisplatin combination chemotherapy in patients with squamous cell carcinoma of the head and neck [J].
Glisson, BS ;
Murphy, BA ;
Frenette, G ;
Khuri, FR ;
Forastiere, AA .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (06) :1593-1599
[6]   RELATIONSHIPS BETWEEN THE STRUCTURE OF TAXOL ANALOGS AND THEIR ANTIMITOTIC ACTIVITY [J].
GUERITTEVOEGELEIN, F ;
GUENARD, D ;
LAVELLE, F ;
LEGOFF, MT ;
MANGATAL, L ;
POTIER, P .
JOURNAL OF MEDICINAL CHEMISTRY, 1991, 34 (03) :992-998
[7]  
Hall AG, 1999, EUR J CLIN INVEST, V29, P238
[8]   Role of Rac1 and oxygen radicals in collagenase-1 expression induced by cell shape change [J].
Kheradmand, F ;
Werner, E ;
Tremble, P ;
Symons, M ;
Werb, Z .
SCIENCE, 1998, 280 (5365) :898-902
[9]   Arsenic trioxide-induced apoptosis and its enhancement by buthionine sulfoximine in hepatocellular carcinoma cell lines [J].
Kito, M ;
Akao, Y ;
Ohishi, N ;
Yagi, K ;
Nozawa, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 291 (04) :861-867
[10]   Synergistic anticancer activity of 1,25-dihydroxyvitamin D3 and immune cytokines:: the involvement of reactive oxygen species [J].
Koren, R ;
Rocker, D ;
Kotestiano, O ;
Liberman, UA ;
Ravid, A .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2000, 73 (3-4) :105-112