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白血病和骨髓增生异常综合征患者红细胞酶及同工酶谱的改变
Study on red cell enzymes and isoenzymes in patients with leukemia and myelodysplastic syndromes
【摘要】 目的:调查白血病和骨髓增生异常综合征(MDS)患者红细胞酶和同工酶谱改变的患病率,并研究其临床意义。方法:采用ICSH介绍的方法及PAGE电泳测定红细胞酶活性及PK和ADA同工酶,采用FPLC系统纯化ADA同工酶,分析酶蛋白的生化性质。结果:患病率:在229例白血病和MDS患者中,G6PD缺乏为43.1%,PK缺乏为27.8%。MDS患者中的酶缺乏患病率:PK缺乏为50.0%,G6PD缺乏为48.0%,PNP缺乏为39.1%;酶过多患病率:ADA过多为69.6%,ENOL过多为40.0%,ALD过多为30.4%。慢性粒细胞白血病(CML)的PK活性增高,而PK同工酶型均正常。急性白血病患者采用抗肿瘤抗生素后G6PD和6PGD活性减低(P<0.05)。MDS红细胞酶缺陷显著多于ADA2同工酶表达见于AML(M4和M5)的单个核细胞及慢性粒-单核细胞白血病(CMML)的红细胞,但ALL不表达(P<0.001)。ADA同工酶纯化分析示正常结构。结论:红细胞酶的检测可作为CML的预后参数,作为急性白血病抗肿瘤药物耐药预示指标,有助于MDS-RA和再障、CML与CMML的鉴别诊断。
【Abstract】 Objective:To define the prevalence of acquired red cell enzymopathy in leukemia and MDS patients and explore its clinical significance.Methods:Red cell enzymes (G6PD,6PGD,PK,ENOL,ADA,PNP,ALD) activities and PK,ADA isoenzymes were assayed by the methods recommended by ICSH and PAGE electrophoresis.Results:The prevalence rate of G6PD deficiency was 43.1%,and of PK deficiency was 27.8%,in leukemia and MDS patients.The prevalence rates of PK,G6PD and PNP deficiency in MDS patients were 50%,48% and 39.1%,respectively,while of ADA,ENOL and ALD over production in MDS patients were 69.6%,40% and 30.4%,respectively.PK activity was increased in CML, while the PK isoenzyme pattern was normal.Administration of antitumor antibiotics to AL decreased G6PD and 6PGD activities (P<0.05).ADA2 was expressed in MNC of AML(M 4 and M 5) and in RBC of CMML,but not expressed in ALL(P<0.001).Conclusion:Determination of enzymes may be used as prognostic parameters in CML,a predictor of antitumor drug resistance in acute leukemia,and a differential parameter between MDS RA and aplastic anemia and between CML and CMML.
【Key words】 Red cell enzymopathy Leukemia Myelodysplastic syndromes;
- 【文献出处】 中华血液学杂志 ,CHINESE JOURNAL OF HEMATOLOGY , 编辑部邮箱 ,1997年07期
- 【分类号】R733.1
- 【被引频次】20
- 【下载频次】47