Effect of polypeptides in bee venom on growth inhibition and apoptosis induction of the human hepatoma cell line SMMC-7721 in-vitro and Balb/c nude mice in-vivo

被引:64
作者
Hu, HY
Chen, DW
Li, YF
Zhang, AG
机构
[1] Shenyang Pharmaceut Univ, Sch Pharm Mailbox 42, Shenyang 110016, Liaoning, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Xian 710049, Shaanxi, Peoples R China
[3] Fourth Mil Med Univ, Sch Basic Med, State Key Lab Canc Biol, Xian 710032, Shanxi, Peoples R China
关键词
D O I
10.1211/jpp.58.1.0010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polypeptides in bee venom (PBV) produced a significant growth inhibition against SMMC-7721 human hepatoma cell line. Analysis of the mechanisms of cell death indicated that PBV induced an apoptotic cell death. SMMC-7721 cells exposed to PBV (10.0 mu g mL(-1)) produced an insignificant morphological change. Analysis of the cytotoxicity with the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium) assay confirmed that the cytotoxic effects of PBV were close- and time-dependent. The result of Ki67 immunohistochemistry demonstrated that the proliferation of SMMC-7721 cells treated with PBV (10.0 mu g mL(-1)) was inhibited. The apoptotic cell death was then confirmed by annexin V, propidium iodide staining and DNA fragmentation analysis. in in-vivo experiments, treatment with PBV (1.5 or 3 mg kg(-1)) resulted in a significant retardation of SMMC-7721 cell growth in Balb/c nude mice. These findings suggested that PBV could be used as a chemotherapeutic agent against tumours.
引用
收藏
页码:83 / 89
页数:7
相关论文
共 36 条
[1]   A novel neurotrophic role of secretory phospholipases A2 for cerebellar granule neurons [J].
Arioka, M ;
Cheon, SH ;
Ikeno, Y ;
Nakashima, S ;
Kitamoto, K .
FEBS LETTERS, 2005, 579 (12) :2693-2701
[2]   Ki67 protein: the immaculate deception? [J].
Brown, DC ;
Gatter, KC .
HISTOPATHOLOGY, 2002, 40 (01) :2-11
[3]  
CHEUNG WY, 1982, FED PROC, V41, P2253
[4]   Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[5]   DNA fragmentation and morphological changes in apoptotic human lymphocytes [J].
Czene, S ;
Testa, E ;
Nygren, J ;
Belyaev, I ;
Harms-Ringdahl, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 294 (04) :872-878
[6]   THE PROLIFERATION-ASSOCIATED KI-67 PROTEIN - DEFINITION IN MOLECULAR TERMS [J].
DUCHROW, M ;
GERDES, J ;
SCHLUTER, C .
CELL PROLIFERATION, 1994, 27 (05) :235-242
[7]   CYTOLYSIS MEDIATED BY IONOPHORES AND PORE-FORMING AGENTS - ROLE OF INTRACELLULAR CALCIUM IN APOPTOSIS [J].
DUKE, RC ;
WITTER, RZ ;
NASH, PB ;
YOUNG, JDE ;
OJCIUS, DM .
FASEB JOURNAL, 1994, 8 (02) :237-246
[8]  
Gerdes J, 1990, Semin Cancer Biol, V1, P199
[9]  
GERDES J, 1984, J IMMUNOL, V133, P1710
[10]   INHIBITION BY MELITTIN AND FLUPHENAZINE OF MELANOTROPIN RECEPTOR FUNCTION AND ADENYLATE-CYCLASE IN M2R MELANOMA CELL-MEMBRANES [J].
GERST, JE ;
SALOMON, Y .
ENDOCRINOLOGY, 1987, 121 (05) :1766-1772