Fedasenka U U, Shman T V, Savitski V P, Belevcev M V
Belarusian Research Center for Pediatric Oncology and Hematology, Minsk, Belarus.
Exp Oncol. 2008 Sep;30(3):248-52.
to investigate properties of leukemic cells by sorting out children diagnosed with ALL with different response to chemotherapy based on MRD level.
We used a minimal residual disease (MRD) data on day 36 obtained with 3-colour flow cytometry as a reference. In view of MRD results, we used real-time PCR to assess expression levels of multidrug resistance associated genes MDR1, LRP and BCRP, antiapoptotic gene Bcl-2 in initial samples from children diagnosed with ALL. P-gp expression and function in initial samples were analyzed by flow cytometry.
Briefly, medians of relative expression levels of MDR1 gene were roughly comparable and in MRD(+) group came to 22.8 (0.02-26.6; n = 9) vs 24.8 (3.9-41.4; n = 10) in MRD(-) group. Bcl-2 gene showed tendency to higher expression levels in MRD(+) group with median at 5992.9 (521.0-10362.0; n = 9) compared to 3183.6 (1947.9-6581.0; n = 10) in MRD(-) group. LRP gene relative expression levels were similar in both groups and came to 1934.9 (1500.7-3490.4; n = 9) and 1408.5 (665.5-2917.1; n = 10) in MRD + and MRD(-) groups, respectively. The median of BCRP expression levels in MRD + group was considerably lower than that in MRD - group, namely 76000.0 (48196.2-169230.8; n = 9) and 227967.2 (16683.7-422222.2; n = 10), respectively, but statistical analysis showed no significant difference for this parameter.
We investigated expression of multidrug resistance genes MDR1, LRP and BCRP and antiapoptotic gene Bcl-2 in leukemic cells at diagnosis, and MRD level at the end of induction therapy, and could not find obvious relations between these parameters.
通过根据微小残留病(MRD)水平对诊断为急性淋巴细胞白血病(ALL)且对化疗有不同反应的儿童进行分类,来研究白血病细胞的特性。
我们将通过三色流式细胞术获得的第36天的微小残留病(MRD)数据作为参考。鉴于MRD结果,我们使用实时聚合酶链反应(PCR)来评估诊断为ALL的儿童初始样本中多药耐药相关基因MDR1、肺耐药相关蛋白(LRP)和乳腺癌耐药蛋白(BCRP)以及抗凋亡基因Bcl-2的表达水平。通过流式细胞术分析初始样本中P-糖蛋白(P-gp)的表达和功能。
简而言之,MDR1基因相对表达水平的中位数大致相当,MRD(+)组为22.8(0.02-26.6;n=9),而MRD(-)组为24.8(3.9-41.4;n=10)。Bcl-2基因在MRD(+)组中显示出较高表达水平的趋势,中位数为5992.9(521.0-10362.0;n=9),而MRD(-)组为3183.6(1947.9-6581.0;n=10)。两组中LRP基因的相对表达水平相似,MRD(+)组和MRD(-)组分别为1934.9(1500.7-3490.4;n=9)和1408.5(665.5-2917.1;n=10)。MRD(+)组中BCRP表达水平的中位数明显低于MRD(-)组,分别为76000.0(48196.2-169230.8;n=9)和227967.2(16683.7-422222.2;n=10),但该参数的统计分析显示无显著差异。
我们研究了诊断时白血病细胞中多药耐药基因MDR1、LRP和BCRP以及抗凋亡基因Bcl-2的表达,以及诱导治疗结束时的MRD水平,未发现这些参数之间存在明显关联。