Jamroziak Krzysztof, Młynarski Wojciech, Balcerczak Ewa, Mistygacz Magda, Trelinska Joanna, Mirowski Marek, Bodalski Jerzy, Robak Tadeusz
Department of Haematology, Medical University of Lodz, ul. Pabianicka 62, 93-513 Lodz, Poland.
Eur J Haematol. 2004 May;72(5):314-21. doi: 10.1111/j.1600-0609.2004.00228.x.
The significance of genetic background in childhood acute lymphoblastic leukemia (ALL) is not well understood. Polymorphisms of genes encoding for xenobiotics and drug transporters are potential factors, which can influence the risk of developing ALL and its clinical outcome. P-glycoprotein (P-gp) is an adenosine triphosphate-binding cassette (ABC)-family transporter involved in protection against xenobiotics and multi-drug resistance. Recently, the single-nucleotide polymorphism C3435T of MDR1 gene has been found to be associated with altered tissue expression and function of P-gp. To evaluate whether C3435T MDR1 polymorphism is associated with the occurrence and outcome of ALL, 113 children with ALL (median age 5.1 yr) and 175 healthy individuals of Polish Caucasian origin were studied by polymerase chain reaction-restriction fragment-length polymorphism (PCR-RFLP) assay. The mutant homozygous TT genotype was found to be associated with occurrence of ALL (OR, 95% CI; 1.8, 1.1-3.1; P = 0.037). Besides, the analysis of factors influencing clinical outcome of our ALL patient cohort showed that CC genotype carriers had significantly lower event-free survival probability (pEFS) (0.62 vs. 0.87; P = 0.007) and overall survival probability (pOS) (0.72 vs. 0.91; P = 0.006). The Cox proportional hazards model-based analysis revealed that the hazard ratios for lower pEFS and lower pOS among CC homozygous subjects were 3.9 (P = 0.008) and 3.3 (P = 0.02), respectively. In conclusion, the results of the present study provide evidence that C3435T MDR1 polymorphism may involve both the susceptibility to and the clinical outcome of childhood ALL. Carriers of the TT genotype are more at risk of developing ALL than other individuals, whereas CC genotype carriers are supposed to have worse prognosis.
遗传背景在儿童急性淋巴细胞白血病(ALL)中的意义尚未得到充分理解。编码外源性物质和药物转运蛋白的基因多态性是潜在因素,可影响ALL的发病风险及其临床结局。P-糖蛋白(P-gp)是一种三磷酸腺苷结合盒(ABC)家族转运蛋白,参与对外源性物质的防护和多药耐药。最近,发现MDR1基因的单核苷酸多态性C3435T与P-gp的组织表达和功能改变有关。为评估C3435T MDR1多态性是否与ALL的发生及结局相关,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析法对113例ALL儿童(中位年龄5.1岁)和175名波兰白种人健康个体进行了研究。发现突变纯合子TT基因型与ALL的发生相关(OR,95%CI:1.8,1.1 - 3.1;P = 0.037)。此外,对影响我们ALL患者队列临床结局的因素分析表明,CC基因型携带者的无事件生存概率(pEFS)显著更低(0.62对0.87;P = 0.007),总生存概率(pOS)也显著更低(0.72对0.91;P = 0.006)。基于Cox比例风险模型的分析显示,CC纯合子受试者中较低pEFS和较低pOS的风险比分别为3.9(P = 0.008)和3.3(P = 0.02)。总之,本研究结果提供了证据表明C3435T MDR1多态性可能既涉及儿童ALL的易感性又涉及其临床结局。TT基因型携带者比其他个体患ALL的风险更高,而CC基因型携带者的预后可能更差。