MDR1 expression correlates with mutant p53 expression in colorectal cancer metastases

被引:30
作者
deKant, E
Heide, I
Thiede, C
Herrmann, R
Rochlitz, CF
机构
[1] KANTONSSPITAL,DEPT INNERE MED,ABT ONKOL,CH-4031 BASEL,SWITZERLAND
[2] UNIV UTRECHT HOSP,DEPT INTERNAL MED G02228,NL-3508 GA UTRECHT,NETHERLANDS
[3] HUMBOLDT UNIV BERLIN,HAMATOL ONKOL ABT,D-13353 BERLIN,GERMANY
关键词
p53; MDR1; colorectal cancer; metastasis;
D O I
10.1007/BF01209030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Overexpression of the multidrug resistance MDR1 gene is thought to contribute to drug resistance in non-responsive cancers like colorectal carcinoma. Little is known about the mechanisms by which expression of MDR1 is regulated in human tumours. However, there is growing evidence that regulation primarily takes place at the transcriptional level and that the process of tumour progression is related to activation of the MDR1 gene. Mutations in the p53 tumour-suppression gene occur in approximately 70% of colorectal cancers. As a transcriptional regulator, p53 might be involved in regulation of MDR1 expression in these tumours. We therefore determined MDR1 expression using the differential polymerase chain reaction technique in 30 colorectal tumours (4 primaries and 26 metastates) and correlated our results with previously reported data on p53 in the same group of patients. We found a significant positive correlation between p53 and MDR1 expression in p53-mutated tumours (P=0.005; r=0.596), but not in tumours without a p53 mutation. In addition, we observed a tendency towards higher MDR1 expression levels in tumours carrying p53 mutations (P=0.14) compound to wild-type p53 tumours. These data indicate that mutant p53 may play a role in the regulation of MDR1 expression in human cholorectal cancer.
引用
收藏
页码:671 / 675
页数:5
相关论文
共 29 条
[1]  
BAKER SJ, 1990, CANCER RES, V50, P7717
[2]  
BANERJEE S, 1992, CELL MOL BIOL, V38, P561
[3]   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
[4]   MODULATION OF ACTIVITY OF THE PROMOTER OF THE HUMAN MDR1 GENE BY RAS AND P53 [J].
CHIN, KV ;
UEDA, K ;
PASTAN, I ;
GOTTESMAN, MM .
SCIENCE, 1992, 255 (5043) :459-462
[5]   P-GLYCOPROTEIN IS NOT EXPRESSED IN A MAJORITY OF COLORECTAL CARCINOMAS AND IS NOT REGULATED BY MUTANT P53 IN-VIVO [J].
DEANGELIS, P ;
STOKKE, T ;
SMEDSHAMMER, L ;
LOTHE, RA ;
LEHNE, G ;
CHEN, Y ;
CLAUSEN, OPF .
BRITISH JOURNAL OF CANCER, 1995, 72 (02) :307-311
[6]  
EFFERTH T, 1992, CANCER DETECT PREV, V16, P237
[7]  
ELROUBY S, 1993, BLOOD, V82, P3452
[8]   EXPRESSION OF A MULTIDRUG-RESISTANCE GENE IN HUMAN-TUMORS AND TISSUES [J].
FOJO, AT ;
UEDA, K ;
SLAMON, DJ ;
POPLACK, DG ;
GOTTESMAN, MM ;
PASTAN, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (01) :265-269
[9]   WILD-TYPE P53 STIMULATES EXPRESSION FROM THE HUMAN MULTIDRUG-RESISTANCE PROMOTER IN A P53-NEGATIVE CELL-LINE [J].
GOLDSMITH, ME ;
GUDAS, JM ;
SCHNEIDER, E ;
COWAN, KH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (04) :1894-1898
[10]   EXPRESSION OF A MULTIDRUG RESISTANCE GENE IN HUMAN CANCERS [J].
GOLDSTEIN, LJ ;
GALSKI, H ;
FOJO, A ;
WILLINGHAM, M ;
LAI, SL ;
GAZDAR, A ;
PIRKER, R ;
GREEN, A ;
CRIST, W ;
BRODEUR, GM ;
LIEBER, M ;
COSSMAN, J ;
GOTTESMAN, MM ;
PASTAN, I .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (02) :116-124