The glutathione-related detoxification pathway in the human breast: a highly coordinated system disrupted in the tumour tissues

被引:34
作者
Perquin, M
Oster, T
Maul, A
Froment, N
Untereiner, M
Bagrel, D
机构
[1] Univ Metz, UFR SciFA, Biochim Lab, F-57070 Metz, France
[2] Univ Metz, Dept Stat & Traitement Informat Donnees, F-57070 Metz, France
[3] Hop Bon Secours, CHR Metz Thionville, Serv Anat Pathol, F-57038 Metz, France
[4] Ctr Natl Radiotherapie, Ctr Francois Badesse, L-4005 Esch Sur Alzette, Luxembourg
关键词
glutathione system; breast cancer; cancer resistance; regulation;
D O I
10.1016/S0304-3835(00)00481-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glutathione and the associated enzymes, glutathione S-transferases, peroxidases, and reductase, have been implicated in cancer chemoresistance. This pathway was investigated in paired cancerous and peritumoral breast samples from 41 women. The tumours exhibited a higher redox status as deduced from increased transferase, peroxidase, and reductase activities and from higher total and reduced glutathione contents. Several components were strongly correlated in peritumoral tissues, suggesting a highly co-ordinated glutathione pathway that appeared disrupted in breast tumours with only a few correlations left. Therefore, resistance could spontaneously result from deregulated variations in the glutathione pathway, which might be relevant to the malignant disease progression. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:7 / 16
页数:10
相关论文
共 33 条
[1]   DIFFERENTIAL ACTIVITY OF HUMAN, RAT, MOUSE AND BACTERIA GLUTATHIONE TRANSFERASE ISOENZYMES TOWARDS 4-NITROQUINOLINE 1-OXIDE [J].
ACETO, A ;
DIILIO, C ;
LOBELLO, M ;
BUCCIARELLI, T ;
ANGELUCCI, S ;
FEDERICI, G .
CARCINOGENESIS, 1990, 11 (12) :2267-2269
[2]   GENETIC-HETEROGENEITY OF THE HUMAN GLUTATHIONE TRANSFERASES - A COMPLEX OF GENE FAMILIES [J].
BOARD, P ;
COGGAN, M ;
JOHNSTON, P ;
ROSS, V ;
SUZUKI, T ;
WEBB, G .
PHARMACOLOGY & THERAPEUTICS, 1990, 48 (03) :357-369
[3]  
Board PG, 1997, BIOCHEM J, V328, P929
[4]  
BONGERS V, 1995, LAB INVEST, V73, P503
[5]  
CAMPBELL JAH, 1991, CANCER, V67, P1608, DOI 10.1002/1097-0142(19910315)67:6<1608::AID-CNCR2820670623>3.0.CO
[6]  
2-S
[7]  
CARLBERG I, 1975, J BIOL CHEM, V250, P5475
[8]   SELENIUM-DEPENDENT AND NON-SELENIUM-DEPENDENT GLUTATHIONE PEROXIDASES IN HUMAN-TISSUE EXTRACTS [J].
CARMAGNOL, F ;
SINET, PM ;
JEROME, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 759 (1-2) :49-57
[9]  
CHAO SSK, 1991, MOL PHARMACOL, V41, P69
[10]  
Coban T, 1998, NEOPLASMA, V45, P151