Gene-expression patterns in drug-resistant acute lymphoblastic leukemia cells and response to treatment

被引:452
作者
Holleman, A
Cheok, MH
den Boer, ML
Yang, WJ
Veerman, AJP
Kazemier, KM
Pei, DQ
Cheng, C
Pui, CH
Relling, MV
Janka-Schaub, GE
Pieters, R
Evans, WE
机构
[1] St Jude Childrens Res Hosp, Dept Pharmaceut Sci, Memphis, TN 38105 USA
[2] Erasmus Univ, Med Ctr, Sophia Childrens Hosp, Div Pediat Hematol Oncol, Rotterdam, Netherlands
[3] St Jude Childrens Res Hosp, Dept Hematol Oncol, Memphis, TN 38105 USA
[4] St Jude Childrens Res Hosp, Dept Biostat, Memphis, TN 38105 USA
[5] Pharmacogenet Res Network, Pharmacogenet Anticanc Agents Res Grp, Memphis, TN USA
[6] Univ Tennessee, Coll Pharm, Memphis, TN USA
[7] Univ Tennessee, Coll Med, Memphis, TN USA
[8] Free Univ Amsterdam, Med Ctr, Dept Pediat Hematol Oncol, Amsterdam, Netherlands
[9] Childrens Univ Hosp, German Cooperat Study Grp Childhood Acute Lymphob, Dept Hematol Oncol, Hamburg, Germany
关键词
D O I
10.1056/NEJMoa033513
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Childhood acute lymphoblastic leukemia (ALL) is curable with chemotherapy in approximately 80 percent of patients. However, the cause of treatment failure in the remaining 20 percent of patients is largely unknown. METHODS: We tested leukemia cells from 173 children for sensitivity in vitro to prednisolone, vincristine, asparaginase, and daunorubicin. The cells were then subjected to an assessment of gene expression with the use of 14,500 probe sets to identify differentially expressed genes in drug-sensitive and drug-resistant ALL. Gene-expression patterns that differed according to sensitivity or resistance to the four drugs were compared with treatment outcome in the original 173 patients and an independent cohort of 98 children treated with the same drugs at another institution. RESULTS: We identified sets of differentially expressed genes in B-lineage ALL that were sensitive or resistant to prednisolone (33 genes), vincristine (40 genes), asparaginase (35 genes), or daunorubicin (20 genes). A combined gene-expression score of resistance to the four drugs, as compared with sensitivity to the four, was significantly and independently related to treatment outcome in a multivariate analysis (hazard ratio for relapse, 3.0; P=0.027). Results were confirmed in an independent population of patients treated with the same medications (hazard ratio for relapse, 11.85; P=0.019). Of the 124 genes identified, 121 have not previously been associated with resistance to the four drugs we tested. CONCLUSIONS: Differential expression of a relatively small number of genes is associated with drug resistance and treatment outcome in childhood ALL.
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收藏
页码:533 / 542
页数:10
相关论文
共 34 条
  • [1] MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia
    Armstrong, SA
    Staunton, JE
    Silverman, LB
    Pieters, R
    de Boer, ML
    Minden, MD
    Sallan, SE
    Lander, ES
    Golub, TR
    Korsmeyer, SJ
    [J]. NATURE GENETICS, 2002, 30 (01) : 41 - 47
  • [2] Treatment-specific changes in gene expression discriminate in vivo drug response in human leukemia cells
    Cheok, MH
    Yang, WL
    Pui, CH
    Downing, JR
    Cheng, C
    Naeve, CW
    Relling, MV
    Evans, WE
    [J]. NATURE GENETICS, 2003, 34 (01) : 85 - 90
  • [3] Treatment-specific changes in gene expression discriminate in vivo drug response in human leukemia cells (vol 34, pg 85, 2003)
    Cheok, MH
    Yang, W
    Pui, CH
    Downing, JR
    Cheng, C
    Naeve, CW
    Relling, MV
    Evans, WE
    [J]. NATURE GENETICS, 2003, 34 (02) : 231 - 231
  • [4] Patient stratification based on prednisolone-vincristine-asparaginase resistance profiles in children with acute lymphoblastic leukemia
    Den Boer, ML
    Harms, DO
    Pieters, R
    Kazemier, KM
    Göbel, U
    Körholz, D
    Graubner, U
    Haas, RJ
    Jorch, N
    Spaar, HJ
    Kaspers, GJL
    Kamps, WA
    Van der Does-Van den Berg, A
    Van Wering, ER
    Veerman, AJP
    Janka-Schaub, GE
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (17) : 3262 - 3268
  • [5] Bagging to improve the accuracy of a clustering procedure
    Dudoit, S
    Fridlyand, J
    [J]. BIOINFORMATICS, 2003, 19 (09) : 1090 - 1099
  • [6] DUI JP, 2003, ZHONGHUA ZHONG LIU Z, V25, P21
  • [7] Moving towards individualized medicine with pharmacogenomics
    Evans, WE
    Relling, MV
    [J]. NATURE, 2004, 429 (6990) : 464 - 468
  • [8] Pharmacogenomics: Translating functional genomics into rational therapeutics
    Evans, WE
    Relling, MV
    [J]. SCIENCE, 1999, 286 (5439) : 487 - 491
  • [9] A proportional hazards model for the subdistribution of a competing risk
    Fine, JP
    Gray, RJ
    [J]. JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1999, 94 (446) : 496 - 509
  • [10] MDM2 induces NF-κB/p65 expression transcriptionally through Sp1-binding sites:: a novel, p53-independent role of MDM2 in doxorubicin resistance in acute lymphoblastic leukemia
    Gu, LB
    Findley, HW
    Zhou, MX
    [J]. BLOOD, 2002, 99 (09) : 3367 - 3375