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作 者:吕晓东[1] 范瑞华[1] 胡杰英[1] 徐本玲[1] 张旭华[1] 郭金东[1] 宋永平[1]
机构地区:[1]河南省肿瘤医院,郑州450008
出 处:《山东医药》2009年第44期18-19,共2页Shandong Medical Journal
基 金:河南省社会公益项目预研专项课题(072103810503)
摘 要:目的探讨定量检测bcr-abl融合基因在慢性粒细胞白血病(CML)诊断、治疗及微小残留病变监测中的意义。方法应用实时定量PCR(RQ-PCR)方法检测145例CML患者bcr-abl融合基因的表达情况。结果abl和bcr-abl的标准曲线相关系数均大于0.99,批内差及批间差均小于4%;11例不同分期的CML患者同时检测外周血和骨髓中bcr-abl水平,8例外周血较骨髓低,3例较骨髓高;急变期的bcr-abl表达情况较加速期和慢性期均明显增高。结论RQ-PCR技术检测bcr-abl融合基因准确可靠,对于评价疗效、监测微小残留病变以及预测疾病进展具有重要的临床应用价值。Objective To evaluate the significance of bcr-abl mRNA expression to diagnose, treat and monitor minimal residual disease in myeloid leukemia (CML). Methods Ber-abl mRNA level of 145 CML patients were detected by realtime quantitative RT-PCR (RQ-PCR). Results Both correlation coefficiencies were over 0.99 for abl and bcr-abl standard curves. Coefficiencies of both interassay and iutraassay variation were below 4%. Detecting bone marrow samples and blood samples of 11 CML cases, levels of bcr-abt expression in 8 patients were lower in blood samples than bone marrow samples, and 3 cases showed higher levels in blood samples. Expression of bcr-abl in blastic phase (BP) was markedly higher than in accelerated phase (AP) and chronic phase (CP) ( P 〈 0. 01 ). Conclusion RQ-PCR is reliable to detect bor-abl gene, which can be used to evaluate the treatment outcome, monitor the minimal residual disease, and predict blast crisis.
关 键 词:白血病 粒细胞 慢性 实时定量PCR bcr—abl融合基因
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