Induction of MRP/GS-X pump and cellular resistance to anticancer prostaglandins

被引:24
作者
Akimaru, K
Kuo, MT
Furuta, K
Suzuki, M
Noyori, R
Ishikawa, T
机构
[1] UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT EXPT PEDIAT,HOUSTON,TX 77030
[2] UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT MOL PATHOL,HOUSTON,TX 77030
[3] GIFU UNIV,DEPT APPL CHEM,GIFU 50111,JAPAN
[4] NAGOYA UNIV,DEPT CHEM,NAGOYA,AICHI 46401,JAPAN
关键词
anticancer prostaglandins; cisplatin; drug resistance; glutathione; GS-X pump; MRP;
D O I
10.1007/BF00744216
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We provide evidence that the expression of the human MRP/GS-Xpump encoded by the MRP (multidrug resistance associated protein) gene is induced by cisplatin in human leukemia HL-60/R-CP (cisplatin-resistant) cells and modulates cell growth inhibition by Delta(7)-prostaglandin A(1) (PGA(1)) methyl ester. The MRP mRNA level in HL-60/R-CP cells increased remarkably after a 24-h incubation with 20 mu M cisplatin; interestingly, however, no amplification of the MRP gene was detected. In cisplatin-sensitive HL-60 cells, which express the MRP/GS-X pump at low levels, c-myc expression was substantially suppressed by Delta(7)-PGA(1) methyl ester and the cell cycle was arrested in G1 phase. By contrast, in HL-60/R-CP cells overexpressing the MRP/GS-X pump, c-myc expression and cell proliferation were much less affected by Delta 7-PGA(1) methyl ester. This suggests that induction of the MRP/GS-X pump may confer on cancer cells resistance to anticancer prostaglandins and that the resistance mechanism may involve the increased efflux of PG-glutathione conjugates, as active intermediates, from the cells via the MRP/GS-X pump.
引用
收藏
页码:221 / 227
页数:7
相关论文
共 18 条
[1]   A 190-KILODALTON PROTEIN OVEREXPRESSED IN NON-P-GLYCOPROTEIN-CONTAINING MULTIDRUG-RESISTANT CELLS AND ITS RELATIONSHIP TO THE MRP GENE [J].
BARRAND, MA ;
HEPPELLPARTON, AC ;
WRIGHT, KA ;
RABBITTS, PH ;
TWENTYMAN, PR .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (02) :110-117
[2]   OVEREXPRESSION OF A TRANSPORTER GENE IN A MULTIDRUG-RESISTANT HUMAN LUNG-CANCER CELL-LINE [J].
COLE, SPC ;
BHARDWAJ, G ;
GERLACH, JH ;
MACKIE, JE ;
GRANT, CE ;
ALMQUIST, KC ;
STEWART, AJ ;
KURZ, EU ;
DUNCAN, AMV ;
DEELEY, RG .
SCIENCE, 1992, 258 (5088) :1650-1654
[3]   THE ATP-DEPENDENT GLUTATHIONE S-CONJUGATE EXPORT PUMP [J].
ISHIKAWA, T .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (11) :463-469
[4]   HOM DOES THE MRP/GS-X PUMP EXPORT DOXORUBICIN [J].
ISHIKAWA, T ;
AKIMARU, K ;
KUO, MT ;
PRIEBE, W ;
SUZUKI, M .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (21) :1639-1640
[5]  
ISHIKAWA T, 1994, J BIOL CHEM, V269, P29085
[6]   EVIDENCE FOR LEUKOTRIENE-C4 TRANSPORT MEDIATED BY AN ATP-DEPENDENT GLUTATHIONE S-CONJUGATE CARRIER IN RAT-HEART AND LIVER PLASMA-MEMBRANES [J].
ISHIKAWA, T ;
KOBAYASHI, K ;
SOGAME, Y ;
HAYASHI, K .
FEBS LETTERS, 1989, 259 (01) :95-98
[7]  
ISHIKAWA T, 1993, STRUCTURE FUNCTION G, P211
[8]  
LEIER I, 1994, J BIOL CHEM, V269, P27807
[9]   The yeast cadmium factor protein (YCF1) is a vacuolar glutathione S-conjugate pump [J].
Li, ZS ;
Szczypka, M ;
Lu, YP ;
Thiele, DJ ;
Rea, PA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (11) :6509-6517
[10]   OVEREXPRESSION OF THE GENE ENCODING THE MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN RESULTS IN INCREASED ATP-DEPENDENT GLUTATHIONE S-CONJUGATE TRANSPORT [J].
MULLER, M ;
MEIJER, C ;
ZAMAN, GJR ;
BORST, P ;
SCHEPER, RJ ;
MULDER, NH ;
DEVRIES, EGE ;
JANSEN, PLM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (26) :13033-13037