摘要
为了建立一种稳定可靠的多药耐药基因(MDR1)mRNA检测方法,探讨MDR1基因表达检测的临床价值,我们采用RT-PCR1方法定量检测了K562、K562/ADM细胞株和30例初治急性白血病MDR1的表达水平。结果发现:1)耐药K562/ADM1细胞系的MDR1表达较高,而K562敏感细胞系无表达。2)初治急性白血病患者MDR1阳性表达率40.0%,表达值为0.2208±0.0896。3)5例正常人对照均无MDR1阳性表达。4)初治急性白血病MDR1阳性表达组缓解率为41.7%,明显低于阴性组88.9%(P<0.01)。我们认为RT-PCR是一种敏感性高、特异性强、可定量检测MDR1表达手段,有临床实用价值;另外,初治急性白血病患者MDR1表达检测的结果表明,MDR1表达增加是化疗的一个不利因素,且对化疗方案的选择有一定的指导意义。
To evaluate the clinical value of the expression of multidrug resistance gene(MDR1) on acute leukemia and to select a reliable quantitative method of expression of MDR1,we analyzed the expression levles of MDR1 in drug-sensitive K562 cell line and multidrug-resisant K562/ADM cell line with RT-PCR. 30 adultuntreated patients were studied by the same tehnique.The results showed that there were a higher lever of MDR1 gene expression in K562/ADM resistant cell line and an undetectable level in K562 sensitive cell line.The MDR1 mRNA positive rates in 30 untreated eases and 5 normal cases were 40. 0% and 0% respectively. All Patients were treated by standard chemotherapy.Complete remission rates were significantly lower in MDR1 mRNA positive group than negative group(41、 7% v 88. 9%P<0. 01). It is conclude that RT-PCR methd is a sensitive quantitation tool for expression of MDR1 and can be used in clinical patients. These data also indicate that MDR1 mRNA expression is an infavorable prognostic factor on diagnosis in acute leukemia and suggest that the levels ofMDR1 mRNA have clinical significance to select the induction chemotherapy regimens.
出处
《中国肿瘤临床》
CAS
CSCD
北大核心
1995年第10期689-693,共5页
Chinese Journal of Clinical Oncology