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EXPRESSION AND CLINICAL SIGNIFICANCE OF MULTIDRUG RESISTANCE GENE AND MULTIDRUG RESISTANCE-ASSOCIATEDPROTEIN GENE IN ACUTE LEUKEMIA
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作者 赖永榕 马劼 +2 位作者 卢玉英 牛威林 向直富 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 1999年第3期192-195,共4页
Objective: To evaluate the expression and clinical significance of multidrug resistance gene (mdr1) and multidrug resistance-associated protein (MRP) gene in acute leukemia. Methods: The expression of mdr1 and MRP ass... Objective: To evaluate the expression and clinical significance of multidrug resistance gene (mdr1) and multidrug resistance-associated protein (MRP) gene in acute leukemia. Methods: The expression of mdr1 and MRP assay in 55 patients with acute leukemia (AL) by reverse transcription polymerase chain reaction (RT-PCR). Results: The mdr1 and MRP gene expression levels in the relapsed AL and the blastic plastic phases of CML were significantly higher than those in the newly diagnostic AL and controls. The mdr1 and MRP gene expression levels in the clinical drug-resistant group were significantly higher than those in the non-drug-resistant group. The complete remission (CR) rate in patients with high mdr1 expression (14.3%) was significantly lower than that with low mdr1 expression (57.5%); similarly the CR rate in patients with high MRP level was also lower than that with low MRP level. Using both high expression of mdr1 and MRP gene as the indicator for evaluating multidrug resistance (MDR), the positive predictive value and accuracy increased in comparison with single gene high expression. Conclusion: Elevated level of mdr1 or MRP gene expression might be unfavorable prognostic factors for AL patient and may be used as an important index for predicting drug-resistance and relapse in AL patient. Measuring both mdr1 and MRP gene expression would increase accuracy and sensibility of evaluating MDR in acute leukemia. 展开更多
关键词 Acute leukemia multidrug resistance gene multidrug resistance-associated protein gene PCR
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黄芩苷对白血病细胞耐药株逆转耐药效果及机制研究 被引量:8
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作者 杨莉洁 赵挺 +1 位作者 白庆咸 董红娟 《陕西医学杂志》 CAS 2012年第7期775-777,779,共4页
目的:观察黄芩苷对白血病耐药株细胞的耐药逆转作用,并初步探讨其可能的机制。方法:MTT法检测阿霉素及黄芩苷对白血病亲本细胞及耐药株细胞的抑制率,通过计算阿霉素对耐药株细胞及亲本细胞的半数抑制浓度(IC50)评价耐药倍数,通过阿霉素... 目的:观察黄芩苷对白血病耐药株细胞的耐药逆转作用,并初步探讨其可能的机制。方法:MTT法检测阿霉素及黄芩苷对白血病亲本细胞及耐药株细胞的抑制率,通过计算阿霉素对耐药株细胞及亲本细胞的半数抑制浓度(IC50)评价耐药倍数,通过阿霉素与黄芩苷联用的IC50评价黄芩苷的逆转作用,流式细胞计数法检测黄芩苷作用后对耐药细胞内阿霉素药物蓄积的影响,RT-PCR检测黄芩苷对耐药细胞中多药耐药相关基因MDR1、MRP1以及LRP1表达的影响。结果:耐药细胞株的耐药倍数为17.384倍,黄芩苷10μg/ml和20μg/ml对白血病耐药株的逆转倍数分别为4.230和7.812,相对逆转率分别为0.81和0.93,黄芩苷作用后耐药株细胞内阿霉素蓄积明显增加,MDR1基因表达显著下降。结论:黄芩苷对白血病耐药细胞株具有显著的逆转作用,其机制可能与下调了细胞内的MDR1基因表达进而抑制P糖蛋白对阿霉素的泵出有关。 展开更多
关键词 黄芩苷 白血病 多药耐药相关蛋白质类 基因表达
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耐药白血病细胞系(K562/H20)MRP表达的实验研究
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作者 夏瑞祥 林果为 +2 位作者 励雁峰 钱耕荪 汪惠园 《安徽医科大学学报》 CAS 1998年第4期249-250,共2页
目的了解MRP在K562/H20耐药株中的表达。方法用32P-dATP标记的MRPcDNA探针,对细胞总RNA进行了Northern杂交。结果与敏感株K562/S相比,K562/H20MRP呈过度表达。结论MRP参与... 目的了解MRP在K562/H20耐药株中的表达。方法用32P-dATP标记的MRPcDNA探针,对细胞总RNA进行了Northern杂交。结果与敏感株K562/S相比,K562/H20MRP呈过度表达。结论MRP参与了K562/H20耐药机制。 展开更多
关键词 白血病 MRP 基因表达 耐药性
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