Expression of resistance-related proteins in tumoral and peritumoral tissues of patients with lung cancer

被引:30
作者
Koomagi, R
Stammler, G
Manegold, C
Mattern, J
Volm, M
机构
[1] GERMAN CANC RES CTR, DEPT ONCOL DIAG & THERAPY, D-69120 HEIDELBERG, GERMANY
[2] THORAX CLIN HEIDELBERG ROHRBACH, D-69126 HEIDELBERG, GERMANY
关键词
resistance; lung tumors; normal tissue; P-glycoprotein; glutathione S-transferase; metallothionein; topoisomerase II; heat shock protein; proto-oncogenes; immunohistochemistry; smoking;
D O I
10.1016/S0304-3835(96)04471-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Twenty tumoral and peritumoral tissues from patients with lung cancer were analyzed immunohistochemically for the drug resistance-related proteins P-glycoprotein (P-170), topoisomerase II (Topo-II), glutathione S-transferase-pi (GST-pi), metallothionein (MT), heat shock protein-70 (HSP-70) and the putative regulators of resistance (ErbB1, Fos and Jun). Protein expression of Topo-II, GST-pi, MT, HSP-70, ErbB1, Fos and Jun was elevated in tumor tissue in comparison to normal tissue. The different expression of the proteins between tumoral and normal tissues was statistically significant for Topo-II (P = 0.05), MT (P = 0.03), and HSP-70 (P = 0.01), whereas ErbB1 showed a borderline significance. The expression of the proteins was frequently increased in smokers in comparison to non-smokers. In general, the increase of the proteins of smokers corresponded in tumoral and non-tumoral tissue. Different expression was only found with MT and HSP-70 which were higher in tissues of smokers.
引用
收藏
页码:129 / 136
页数:8
相关论文
共 56 条
[1]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[2]  
BATIST G, 1986, J BIOL CHEM, V261, P5544
[3]   GLUTATHIONE S-TRANSFERASES - BIOMEDICAL APPLICATIONS [J].
BECKETT, GJ ;
HAYES, JD .
ADVANCES IN CLINICAL CHEMISTRY, VOL 30, 1993, 30 :281-380
[4]   ROLE OF GLUTATHIONE AND ITS ASSOCIATED ENZYMES IN MULTIDRUG-RESISTANT HUMAN MYELOMA CELLS [J].
BELLAMY, WT ;
DALTON, WS ;
MELTZER, P ;
DORR, RT .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (05) :787-793
[5]   TRANSFORMATION OF RAT-LIVER EPITHELIAL-CELLS WITH V-H-RAS OR V-RAF CAUSES EXPRESSION OF MDR-1, GLUTATHIONE-S-TRANSFERASE-P AND INCREASED RESISTANCE TO CYTO-TOXIC CHEMICALS [J].
BURT, RK ;
GARFIELD, S ;
JOHNSON, K ;
THORGEIRSSON, SS .
CARCINOGENESIS, 1988, 9 (12) :2329-2332
[6]   GLUTATHIONE S-TRANSFERASE ISOENZYMES AND GLUTATHIONE-PEROXIDASE ACTIVITY IN NORMAL AND TUMOR SAMPLES FROM HUMAN-LUNG [J].
CARMICHAEL, J ;
FORRESTER, LM ;
LEWIS, AD ;
HAYES, JD ;
HAYES, PC ;
WOLF, CR .
CARCINOGENESIS, 1988, 9 (09) :1617-1621
[7]  
CARR DT, 1977, CLIN DIAGNOSIS TREAT, P151
[8]  
CIOCCA DR, 1992, CANCER RES, V52, P3648
[9]  
DEFFIE A M, 1989, Proceedings of the American Association for Cancer Research Annual Meeting, V30, P514
[10]  
DRINGS P, 1994, STRAHLENTHER ONKOL, V9, P495