BCRP gene expression is associated with a poor response to remission induction therapy in childhood acute myeloid leukemia

被引:180
作者
Steinbach, D [1 ]
Sell, W [1 ]
Voigt, A [1 ]
Hermann, J [1 ]
Zintl, F [1 ]
Sauerbrey, A [1 ]
机构
[1] Univ Childrens Hosp, Jena, Germany
关键词
multidrug resistance; BCRP; prognosis; childhood AML;
D O I
10.1038/sj.leu.2402541
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer resistance protein (BCRP), also known as mitoxantrone resistance protein (MRX) or placenta ABC protein (ABC-P), is the second member of the ABCG subfamily of ABC transport proteins (gene symbol ABCG2). Transfection and enforced expression of BCRP in drug-sensitive cells confers resistance to mitoxantrone, doxorubicin, daunorubicin and topotecan. In this study the expression of BCRP gene was measured using TaqMan real-time PCR in 59 children with newly diagnosed AML. Nine patients were also analyzed in relapse. The median of BCRP gene expression was more than 10 times higher in patients who did not achieve remission after the first phase of chemotherapy (n = 24) as compared to patients who did achieve remission at this stage (n = 21; P = 0.012). In first relapse the expression of the BCRP gene was higher than at diagnosis (P = 0.038). Although high levels of BCRP gene expression were more frequent in subtypes of AML with a favorable prognosis, we found that within both risk groups (high and low risk), patients who expressed high levels of BCRP had a worse prognosis (P = 0.023). Our results strongly suggest that the expression of the BCRP gene reduces the response to chemotherapy in AML and that BCRP expression is higher at the time of relapse.
引用
收藏
页码:1443 / 1447
页数:5
相关论文
共 22 条
[1]  
Allikmets R, 1998, CANCER RES, V58, P5337
[2]   Idarubicin improves blast cell clearance during induction therapy in children with AML:: results of study AML-BFM 93 [J].
Creutzig, U ;
Ritter, J ;
Zimmermann, M ;
Hermann, J ;
Gadner, H ;
Sawatzki, DB ;
Niemeyer, CM ;
Schwabe, D ;
Selle, B ;
Boos, J ;
Kühl, J ;
Feldges, A .
LEUKEMIA, 2001, 15 (03) :348-354
[3]   A multidrug resistance transporter from human MCF-7 breast cancer cells [J].
Doyle, LA ;
Yang, WD ;
Abruzzo, LV ;
Krogmann, T ;
Gao, YM ;
Rishi, AK ;
Ross, DD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15665-15670
[4]  
Filipits M, 1997, CLIN CANCER RES, V3, P1419
[5]   PREDICTIVE VALUE FOR TREATMENT OUTCOME IN ACUTE MYELOID-LEUKEMIA OF CELLULAR DAUNORUBICIN ACCUMULATION AND P-GLYCOPROTEIN EXPRESSION SIMULTANEOUSLY DETERMINED BY FLOW-CYTOMETRY [J].
GUERCI, A ;
MERLIN, JL ;
MISSOUM, N ;
FELDMANN, L ;
MARCHAL, S ;
WITZ, F ;
ROSE, C ;
GUERCI, O .
BLOOD, 1995, 85 (08) :2147-2153
[6]  
LAMY T, 1994, LEUKEMIA, V8, P1879
[7]  
Leith CP, 1999, BLOOD, V94, P1086
[8]  
Maliepaard M, 2001, CANCER RES, V61, P3458
[9]  
Miyake K, 1999, CANCER RES, V59, P8
[10]   The product of the ABC half-transporter gene ABCG2 (BCRP/MXR/ABCP) is expressed in the plasma membrane [J].
Rocchi, E ;
Khodjakov, A ;
Volk, EL ;
Yang, CH ;
Litman, T ;
Bates, SE ;
Schneider, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 271 (01) :42-46