Differential expression of sphingolipids in P-glycoprotein or multidrug resistance-related protein 1 expressing human neuroblastoma cell lines

被引:18
作者
Dijkhuis, AJ
Douwes, J
Kamps, W
Sietsma, H
Kok, JW
机构
[1] Univ Groningen, GUIDE, Dept Membrane Cell Biol, NL-9713 AV Groningen, Netherlands
[2] Beatrix Childrens Hosp, Dept Pediat, Div Pediat Oncol, NL-9713 GZ Groningen, Netherlands
[3] Univ Groningen Hosp, Dept Pathol, NL-9713 GZ Groningen, Netherlands
来源
FEBS LETTERS | 2003年 / 548卷 / 1-3期
关键词
neuroblastoma; sphingolipid; ganglioside; multidrug resistance; P-glycoprotein; multidrug resistance-related protein 1;
D O I
10.1016/S0014-5793(03)00721-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sphingolipid composition and multidrug resistance status of three human neuroblastoma cell lines were established. SK-N-FI cells displayed high expression and functional (efflux) activity of P-glycoprotein, while multidrug resistance-related protein 1 was relatively abundant and most active in SK-N-AS cells. These two cell lines exhibited higher sphingolipid levels, compared to SK-N-DZ, which had the lowest activity of either ATP-binding cassette transporter protein. SK-N-DZ cells also differed in ganglioside composition with predominant expression of b-series gangliosides. In conclusion, these three neuroblastoma cell lines offer a good model system to study sphingolipid metabolism in relation to ATP-binding cassette transporter protein function. (C) 2003 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:28 / 32
页数:5
相关论文
共 20 条
[1]  
BLIGHT EJ, 1959, CAN J BIOCH PHYSL, V13, P911
[2]  
CARMICHAEL J, 1987, CANCER RES, V47, P936
[3]  
Kaucic K, 2001, CANCER, V91, P785, DOI 10.1002/1097-0142(20010215)91:4<785::AID-CNCR1065>3.0.CO
[4]  
2-R
[5]  
Kok JW, 2000, INT J CANCER, V87, P172, DOI 10.1002/1097-0215(20000715)87:2<172::AID-IJC3>3.0.CO
[6]  
2-K
[7]   A SOLVENT PARTITION METHOD FOR MICROSCALE GANGLIOSIDE PURIFICATION [J].
LADISCH, S ;
GILLARD, B .
ANALYTICAL BIOCHEMISTRY, 1985, 146 (01) :220-231
[8]   Accumulation of glucosylceramides in multidrug-resistant cancer cells [J].
Lavie, Y ;
Cao, HT ;
Bursten, SL ;
Giuliano, AE ;
Cabot, MC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (32) :19530-19536
[9]   Expression of glucosylceramide synthase, converting ceramide to glucosylceramide, confers adriamycin resistance in human breast cancer cells [J].
Liu, YY ;
Han, TY ;
Giuliano, AE ;
Cabot, MC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (02) :1140-1146
[10]   Ceramide glycosylation potentiates cellular multidrug resistance [J].
Liu, YY ;
Han, TY ;
Giuliano, AE ;
Cabot, MC .
FASEB JOURNAL, 2001, 15 (03) :719-730