Metabolic alterations in K562 cells exposed to taxol and tyrphostin AG957:: 1H NMR and biochemical studies

被引:13
作者
Knijn, A
Brisdelli, F
Ferretti, A
Iorio, E
Marcheggiani, D
Bozzi, A [1 ]
机构
[1] Univ Aquila, Dept Biomed Sci & Technol, I-67100 Laquila, Italy
[2] Ist Super Sanita, Data Management Serv, I-00161 Rome, Italy
[3] Ist Super Sanita, Cell Biol Lab, I-00161 Rome, Italy
关键词
glutathione; phosphorylcholine; Myo-inositol; taxol; tyrphostin AG957;
D O I
10.1016/j.cellbi.2005.07.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
K562 cells exposed for 3 h to taxol or taxol plus tyrphostin AG957 exhibited a significant variation in the concentration of the water-soluble metabolites glutathione, myo-inositol and phosphoryleholine, as evaluated by H-1 NMR up to 72 h incubation in drug-free medium. Cells treated with both drugs showed an increase of glutathione and glutathione reductase at 24 h and a sharp decrease of myo-inositol between 8 and 24 h. Phosphorylcholine increased at 8 h both in taxol and taxol plus AG957-treated cells, which was then abruptly inverted to a significantly lower concentration at 24 h, subsequently increasing again to values higher than those found in taxol-treated and control cells. All the above reported effects were lacking in cells exposed to AG957 alone. These modifications, despite the enhancement of the overall apoptotic cascade in taxol plus AG957-treated cells, can be related to the activation of cellular detoxification mechanisms, to the correct osmolarity maintenance, and to alterations of phospholipid metabolism. (c) 2005 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:890 / 897
页数:8
相关论文
共 35 条
[1]  
ANDERSON ME, 1985, METHOD ENZYMOL, V113, P548
[2]   Tyrosine kinase inhibitors and immunosuppressants perturb the myo-inositol but not the betaine cotransporter in isotonic and hypertonic MDCK cells [J].
Atta, MG ;
Dahl, SC ;
Kwon, HM ;
Handler, JS .
KIDNEY INTERNATIONAL, 1999, 55 (03) :956-962
[3]  
Au JLS, 1998, CANCER RES, V58, P2141
[4]  
Beran M, 1998, CLIN CANCER RES, V4, P1661
[5]   TNF-induced modulations of phospholipid metabolism in human breast cancer cells [J].
Bogin, L ;
Papa, MZ ;
Polak-Charcon, S ;
Degani, H .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1998, 1392 (2-3) :217-232
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   The putative benzene metabolite 2,3,5-tris(glutathion-S-yl)hydroquinone depletes glutathione, stimulates sphingomyelin turnover, and induces apoptosis in HL-60 cells [J].
Bratton, SB ;
Lau, SS ;
Monks, TJ .
CHEMICAL RESEARCH IN TOXICOLOGY, 2000, 13 (07) :550-556
[8]   Two-step formation of lH NMR visible mobile lipids during apoptosis of paclitaxel-treated K562 cells [J].
Brisdelli, F ;
Iorio, E ;
Knijn, A ;
Ferretti, A ;
Marcheggiani, D ;
Lenti, L ;
Strom, R ;
Podo, F ;
Bozzi, A .
BIOCHEMICAL PHARMACOLOGY, 2003, 65 (08) :1271-1280
[9]  
CARLBERG I, 1975, J BIOL CHEM, V250, P5475
[10]   Phosphatidylcholine and cell death [J].
Cui, Z ;
Houweling, M .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2002, 1585 (2-3) :87-96