Multidrug Resistance Mediated by MRP1 Gene Overexpression in Breast Cancer Patients

被引:25
作者
Abaan, Ogan Demir [1 ,2 ]
Mutlu, Pelin Kaya [1 ]
Baran, Yusuf [1 ,3 ]
Atalay, Can [1 ,4 ]
Gunduz, Ufuk [1 ]
机构
[1] Middle E Tech Univ, Dept Biol, TR-06531 Ankara, Turkey
[2] Georgetown Univ, Dept Oncol, Lombardi Comphrenes Canc Ctr, Washington, DC USA
[3] Izmir Inst Technol, Dept Mol Biol & Genet, Izmir, Turkey
[4] Ankara Oncol Hosp, Dept Gen Surg, Ankara, Turkey
关键词
Multidrug resistance; MDR; MRP1; Breast cancer; Chemotherapy; MRP Family; HUMAN TUMOR-CELLS; LEUKEMIA-CELLS; PROTEIN MRP; DRUG-RESISTANCE; EXPRESSION; CARCINOMA; MDR1;
D O I
10.1080/07357900802173562
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Multidrug resistance (MDR) is a serious handicap towards the effective treatment of breast cancer patients. One of the most prevalent MDR mechanisms is through the overexpression of genes coding the proteins called Multidrug Resistance-associated Proteins (MRPs). The aim of this study was to investigate the expression of MRP1 in tumor tissues from breast cancer patients. In this study, a semi-quantitative RT-PCR approach was utilized. Our results suggest that MRP1 overexpression can mediate MDR in patients. Pre-evaluation of the level of such MDR mediators before chemotherapy can increase the efficacy of the treatment.
引用
收藏
页码:201 / 205
页数:5
相关论文
共 19 条
[1]
Baran Y., 2006, Experimental Oncology, V28, P163
[2]
Upregulation of multi drug resistance genes in doxorubicin resistant human acute myelogeneous leukemia cells and reversal of the resistance [J].
Baran, Yusuf ;
Guer, Bala ;
Kaya, Pelin ;
Ural, Ali Ugur ;
Avcu, Ferit ;
Guenduez, Ufuk .
HEMATOLOGY, 2007, 12 (06) :511-517
[3]
COLE SPC, 1994, CANCER RES, V54, P5902
[4]
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
[5]
Dexter DW, 1998, CLIN CANCER RES, V4, P1533
[6]
Ferrero JM, 2000, BRIT J CANCER, V82, P171
[7]
Lack of glutathione conjugation to adriamycin in human breast cancer MCF-7/DOX cells -: Inhibition of glutathione S-transferase P1-1 by glutathione conjugates from anthracyclines [J].
Gaudiano, G ;
Koch, TH ;
Lo Bello, M ;
Nuccetelli, M ;
Ravagnan, G ;
Serafino, A ;
Sinibaldi-Vallebona, P .
BIOCHEMICAL PHARMACOLOGY, 2000, 60 (12) :1915-1923
[8]
Rapid RNA isolation without the use of commercial kits: Application to small tissue samples [J].
Gauthier, ER ;
Madison, SD ;
Michel, RN .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1997, 433 (05) :664-668
[9]
Meeting highlights:: Updated international expert consensus on the primary therapy of early breast cancer [J].
Goldhirsch, A ;
Wood, WC ;
Gelber, RD ;
Coates, AS ;
Thürlimann, B ;
Senn, HJ .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (17) :3357-3365
[10]
GRANT CE, 1994, CANCER RES, V54, P357