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GSTM1基因多态性与白血病关系的研究 被引量:3

Relation of GSTM1 Polymorphism with Leukemia
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摘要 目的:探讨白血病患者GSTM1基因多态性与白血病疗效及主要生物学特征的关系。方法:采用巢式PCR检测GSTM1基因型,比较不同基因型患者第1疗程的缓解率及发病时的主要生物学特征。结果:GSTM1非缺失基因型患者第1疗程的缓解率及部分缓解率与GSTM1缺失基因型无显著性差异(χ~2=0.290,P=0.590);GSTM1基因型与患者性别、年龄,初诊时白细胞数、血红蛋白水平、血小板数、脾脏肿大无相关性(P>0.05);用Log-rank法对GSTM1缺失基因型的AML与ALL组比较结果显示,AML与ALL组患者的生存率之间无统计学差异(χ~2=2.043,P=0.153);GSTM1未缺失基因型患者初诊时血清乳酸脱氢酶浓度与GSTM1缺失基因型比较有统计学差异(P=0.001)。结论:GSTM1基因型与白血病患者第1疗程的缓解及部分缓解率无相关性,GSTM1基因型与患者血清乳酸脱氢酶浓度有关。 Objective: To investigate the relation of GSTM1 polymorphism in leukemia patients with therapeutic efficacy and the main biological characteristics. Methods: The GSTM] genotypes were detected by nested PCR; the remission rate after 1 course of treatment and main biological characteristics at occurrence of leukemia were compared between AL patients with different GSTM1 genotypes, and their relation was analyzed. Results: The remission rate and partial remission rate after 1 course of treatment in patients with GSTMl-undeleted genotype were no significantly different from those in patients with GSTM1 null genotype ( χ^2= 0.290, P 〉 0.05 ). The stratification analysis showed that GSTM1 null genotype was not related with age, sex, WBC count, Hb level, pit count at initial diagnosis and spleen enlargenent or no( P 〉 0.05 ). The comparison of AML and ALL with GSTM1 null genotype by Log-rank showed that the survival rate was no statistically different between AML and ALL patients (χ^2 = 2.043, P 〉 0.05 ), while the LDH level in serum of patients with GSTMl-undeleted genotype at initial diagnosis was statistically different from that in patients with GSTM1 null genotype (P = 0. 001 ). Conclusion: The GSTM1 genotype does not relate with remission and partial remission rates after 1 course treatment of AL patients, but relates with LDH level. GSTM1 null genotype deletion may play a role in risk of leukemia.
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2017年第2期318-321,共4页 Journal of Experimental Hematology
基金 兰州市自然科学基金(2011-2-46)
关键词 白血病 GSTM1基因 LDH leukemia GSTM1 gene LDH
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