Selective antiproliferative and apoptotic effects of flavonoids purified from Rhus verniciflua Stokes on normal versus transformed hepatic cell lines

被引:80
作者
Son, YO
Lee, KY
Lee, JC
Jang, HS
Kim, JG
Jeon, YM
Jang, YS
机构
[1] Div Biol Sci, Chonju 561756, South Korea
[2] Res Ctr Bioact Mat, Chonju 561756, South Korea
[3] Chonbuk Natl Univ, Cell Biol Lab, Dept Orthodont, Chonju 561756, South Korea
[4] Chonbuk Natl Univ, Inst Oral Biosci, Chonju 561756, South Korea
[5] Korea Univ, Coll Med, Dept Dent Oral & Maxillofacial Surg, Ansan 425020, South Korea
关键词
Rhus verniciflua Stokes; flavonoids; Hepatocytes; selective growth inhibition; apoptosis;
D O I
10.1016/j.toxlet.2004.09.003
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Considerable attention is being concentrated on dietary flavonoids in developing novel cancer-preventive approaches due to their potential ability to induce selective apoptosis of cancer cells. In this study, we prepared a flavonoid-containing fraction from a crude acetone extract of Rhus verniciflua Stokes (RVS), traditionally used as a food additive and as an herbal medicine, and named RVS chloroform-methanol fraction (RCMF). We evaluated the effects of RCMF on proliferation and apoptosis using mouse embryonic primary hepatic cells (MPHC), embryonic normal hepatic cell line (BNL CL.2), and its SV40-mediated transformed cell line (BNL SV A.8). We also investigated the effects of RCMF on the antioxidant defense system in those cells. This study demonstrated that RCMF exhibited a selective growth inhibition and apoptosis induction on transformed cells. BNL SV A.8 cells were more sensitive to RCMF-mediated cytotoxicity than were MPHC or BNL CL.2. RCMF-mediated reduction of MnSOD activity and glutathione (GSH) content in BNL SV A.8 cells is thought to be associated with RCMF-induced apoptosis. Our findings suggest that RCMF is an agent which may be capable of inducing growth inhibition and apoptosis of hepatic tumor cells. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:115 / 125
页数:11
相关论文
共 44 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]  
Caltagirone S, 2000, INT J CANCER, V87, P595, DOI 10.1002/1097-0215(20000815)87:4&lt
[3]  
595::AID-IJC21&gt
[4]  
3.0.CO
[5]  
2-5
[6]   Treatment of plasma cell leukemia with vincristine, liposomal doxorubicin and dexamethasone [J].
Christou, L ;
Hatzimichael, E ;
Chaidos, A ;
Tsiara, S ;
Bourantas, KL .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2001, 67 (01) :51-53
[7]   Glutathione content as an indicator for the presence of metabolic pathways of amino acids in astroglial cultures [J].
Dringen, R ;
Hamprecht, B .
JOURNAL OF NEUROCHEMISTRY, 1996, 67 (04) :1375-1382
[8]   VASODILATOR EFFECTS OF QUERCETIN IN ISOLATED RAT VASCULAR SMOOTH-MUSCLE [J].
DUARTE, J ;
PEREZVIZCAINO, F ;
ZARZUELO, A ;
JIMENEZ, J ;
TAMARGO, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 239 (1-3) :1-7
[9]   Review of the biology of quercetin and related bioflavonoids [J].
Formica, JV ;
Regelson, W .
FOOD AND CHEMICAL TOXICOLOGY, 1995, 33 (12) :1061-1080
[10]   Flavonoids and the inhibition of PKC and PI 3-kinase [J].
Gamet-Payrastre, L ;
Manenti, S ;
Gratacap, MP ;
Tulliez, J ;
Chap, H ;
Payrastre, B .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1999, 32 (03) :279-286