THE EFFECT OF MDR-1 GENE-EXPRESSION ON OUTCOME IN ACUTE MYELOBLASTIC-LEUKEMIA

被引:53
作者
HOLMES, JA [1 ]
WEST, RR [1 ]
机构
[1] UNIV WALES COLL CARDIFF,COLL MED,DEPT EPIDEMIOL,CARDIFF CF4 4XN,S GLAM,WALES
关键词
D O I
10.1038/bjc.1994.70
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Resistance to cytotoxic agents may be encountered during the treatment of acute myeloblastic leukaemia (AML). P-glycoprotein encoded by the MDR-I gene has been implicated as a potential drug resistance mechanism in leukaemic cells. In recent years, many data have been accrued concerning the expression of P-glycoprotein in leukaemia, and several studies have been published which have related MDR status to outcome in AML. Conclusions as to the effect of P-glycoprotein expression on prognosis in AML have varied widely. The studies are not immediately comparable, since they differ in methodology, treatment regimens, demographic profile and, perhaps most importantly, criteria for positivity of MDR status. The technique of statistical overview (meta-analysis) can be used to poor observational studies. Application of this statistical method to existing studies suggests an estimated relative risk of 0.68 for P-glycoprotein expression with respect to complete remission in AML. Further large studies are required to determine fully the role of P-glycoprotein in AML.
引用
收藏
页码:382 / 384
页数:3
相关论文
共 23 条
[1]  
BALL ED, 1990, BLOOD S, V76, pA252
[2]   PUBLICATION BIAS - A PROBLEM IN INTERPRETING MEDICAL DATA [J].
BEGG, CB ;
BERLIN, JA .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES A-STATISTICS IN SOCIETY, 1988, 151 :419-463
[3]  
BIEDLER JL, 1970, CANCER RES, V30, P1174
[4]   MECHANISM OF MULTIDRUG RESISTANCE [J].
BRADLEY, G ;
JURANKA, PF ;
LING, V .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 948 (01) :87-128
[5]  
CAMPOS L, 1992, BLOOD, V79, P473
[6]   INTERNAL DUPLICATION AND HOMOLOGY WITH BACTERIAL TRANSPORT PROTEINS IN THE MDR1 (P-GLYCOPROTEIN) GENE FROM MULTIDRUG-RESISTANT HUMAN-CELLS [J].
CHEN, CJ ;
CHIN, JE ;
UEDA, K ;
CLARK, DP ;
PASTAN, I ;
GOTTESMAN, MM ;
RONINSON, IB .
CELL, 1986, 47 (03) :381-389
[7]   MDR1/P-GLYCOPROTEIN GENE SEGMENTS ANALYZED FROM VARIOUS HUMAN LEUKEMIC-CELL LINES EXHIBITING DIFFERENT MULTIDRUG RESISTANCE PROFILES [J].
GEKELER, V ;
WEGER, S ;
PROBST, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 169 (02) :796-802
[8]   QUANTITATIVE-DETERMINATION OF MDR1 GENE-EXPRESSION IN LEUKEMIC-CELLS FROM PATIENTS WITH ACUTE-LEUKEMIA [J].
GRUBER, A ;
VITOLS, S ;
NORGREN, S ;
ARESTROM, I ;
PETERSON, C ;
BJORKHOLM, M ;
REIZENSTEIN, P ;
LUTHMAN, H .
BRITISH JOURNAL OF CANCER, 1992, 66 (02) :266-272
[9]  
HOLMES JA, 1992, LEUKEMIA, V6, P484
[10]   SURFACE GLYCOPROTEIN MODULATING DRUG PERMEABILITY IN CHINESE-HAMSTER OVARY CELL MUTANTS [J].
JULIANO, RL ;
LING, V .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 455 (01) :152-162