Expression of genes related to multiple drug resistance and apoptosis in acute leukemia: response to induction chemotherapy

被引:49
作者
Chauhan, Pradeep Singh [1 ]
Bhushan, Bharat [1 ]
Singh, L. C. [1 ]
Mishra, Ashwani Kumar [1 ]
Saluja, Sumita [2 ]
Mittal, Vishakha [2 ]
Gupta, Dipendra Kumar [2 ]
Kapur, Sujala [1 ]
机构
[1] Natl Inst Pathol ICMR, New Delhi 110029, India
[2] Safdarjang Hosp, Dept Hematol, New Delhi 110029, India
关键词
Drug resistance gene; Apoptotic gene; Real-time PCR; Acute leukemia; Induction chemotherapy; ACUTE MYELOID-LEUKEMIA; MULTIDRUG-RESISTANCE; P-GLYCOPROTEIN; PROGNOSTIC-SIGNIFICANCE; MESSENGER-RNA; CHILDHOOD; SURVIVIN; PROTEINS; BCL-2; PCR;
D O I
10.1016/j.yexmp.2011.09.004
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
Resistance to chemotherapy is a major impediment to the successful treatment of acute leukemia (AL). Expression of genes involved in drug resistance and apoptosis may be responsible for this. This study aimed to investigate the expression of drug resistance (MDR1, MRP1, LRP, BCRP, GSTP1, DHFR) and apoptotic genes (p53, BCL-2, Survivin) in adult acute leukemias and compare them with clinical and hematological findings and response to induction chemotherapy. Eighty-five patients with AL [45 with acute myeloid leukemia (AML) and 40 with acute lymphoblastic leukemia (ALL)] were used as a study group. Real-time PCR results showed that expression level of MDR1 was significantly higher in AML whereas expression of DHFR, BCRP and Survivin was significantly higher in All patients. In AML, significant correlation was observed between LRP and MRP1 (r(s) = 0.44, p=0.016). LRP and DHFR (r(s) = 0.41, p = 0.02), MDR1 and BCL-2 (r(s) = 0.38, p = 0.03). Expression of GSTP1 and LRP correlated with high white blood count (p = 0.03 and p = 0.03) and BCL-2 with high peripheral blast count (p = 0.009). MDR1 expression was significantly associated with the expression of immature stem cell marker CD34 (p = 0.002). In ALL significant association was found between LRP gene and female sex (p<0.0001), LRP and B-ALL patients (p = 0.04) and LRP and BCR/ABL positive patients (p = 0.004). High expression of MDR1 and BCL-2 in AML and MRP1 gene in ALL was associated with response to induction chemotherapy (p = 0.001, p = 0.02 and p = 0.007 respectively). These results showed the potential clinical relevance of MDR1, MRP1 and BCL-2 in adult patients with acute leukemia in the context of induction chemotherapy. (C) 2011 Elsevier Inc. All rights reserved.
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页码:44 / 49
页数:6
相关论文
共 32 条
[1]
Expression and prognostic significance of survivin in de novo acute myeloid leukaemia [J].
Adida, C ;
Recher, C ;
Raffoux, E ;
Daniel, MT ;
Taksin, AL ;
Rousselot, P ;
Sigaux, F ;
Degos, L ;
Altieri, DC ;
Dombret, H .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 111 (01) :196-203
[2]
Anti-apoptosis gene, survivin, and prognosis of neuroblastoma [J].
Adida, C ;
Berrebi, D ;
Peuchmaur, M ;
Reyes-Mugica, M ;
Altieri, DC .
LANCET, 1998, 351 (9106) :882-883
[3]
MRP3, BCRR and P-glycoprotein activities are prognostic factors in adult acute myeloid leukemia [J].
Benderra, Z ;
Faussat, AM ;
Sayada, L ;
Perrot, JY ;
Tang, RP ;
Chaoui, D ;
Morjani, H ;
Marzac, C ;
Marie, JP ;
Legrand, O .
CLINICAL CANCER RESEARCH, 2005, 11 (21) :7764-7772
[4]
BERTINO JR, 1977, CANCER TREAT REP, V61, P667
[5]
Aberrant phenotypes in childhood and adult acute leukemia and its association with adverse prognostic factors and clinical outcome [J].
Bhushan, Bharat ;
Chauhan, Pradeep Singh ;
Saluja, Sumita ;
Verma, Saurabh ;
Mishra, Ashwani Kumar ;
Siddiqui, Saeed ;
Kapur, Sujala .
CLINICAL AND EXPERIMENTAL MEDICINE, 2010, 10 (01) :33-40
[6]
Mutation of FLT3 gene in acute myeloid leukemia with normal cytogenetics and its association with clinical and immunophenotypic features [J].
Chauhan, Pradeep S. ;
Bhushan, Bharat ;
Mishra, Ashwani K. ;
Singh, Laishram C. ;
Saluja, Sumita ;
Verma, Saurabh ;
Gupta, Dipendra K. ;
Mittal, Vishakha ;
Chaudhry, Sumita ;
Kapur, Sujala .
MEDICAL ONCOLOGY, 2011, 28 (02) :544-551
[7]
CROSS NCP, 1994, LEUKEMIA, V8, P186
[8]
Different expression of glutathione S-transferase α, μ and π in childhood acute lymphoblastic and myeloid leukaemia [J].
Den Boer, ML ;
Pieters, R ;
Kazemier, KM ;
Janka-Schaub, GE ;
Henze, G ;
Creutzig, U ;
Kaspers, GJL ;
Kearns, PR ;
Hall, AG ;
Pearson, ADJ ;
Veerman, AJP .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 104 (02) :321-327
[9]
Expression of the lung resistance protein predicts poor outcome in de novo acute myeloid leukemia [J].
Filipits, M ;
Pohl, G ;
Stranzl, T ;
Suchomel, RW ;
Scheper, RJ ;
Jäger, U ;
Geissler, K ;
Lechner, K ;
Pirker, R .
BLOOD, 1998, 91 (05) :1508-1513
[10]
Galimberti S, 2003, ANTICANCER RES, V23, P3419