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浙江大学学报(医学版)  1995, Vol. 24 Issue (2): 49-51    DOI: 10.3785/j.issn.1008-9292.1995.02.001
论著     
用逆转录多聚酶链反应法检测多药耐药基因(mdr 1)的表达
杨骅1, 曹江1, 胡汛1, 郑树1, 董海涛2
1. 浙江医科大学肿瘤研究所;
2. 浙江医科大学医学分子生物实验室
ANALYSIS OF MDR 1 GENE EXPRESSION BY REVERSE TRANSCRIPTION-POL YMERASE CHAIN REACTION
Yang Hua1, Dong Haitao1, Cao Jiang1, et al
Cancer Intstitute, Zhejiang Medical University
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摘要:

以长春新碱诱导的耐药细胞K562/VCR和阿霉素诱导的耐药细胞K562/DOX及敏感细胞K562作为检测对象,采用逆转录多聚酶链反应法,并且以β2-微球蛋白(β2m)基因作为内参照,检测和比较了上述细胞的多药耐药基因mdr 1表达。经过30个循环扩增,耐药细胞检测出mdr 1和β2m基因的扩增产物,而敏感细胞无mdr 1扩增产物。结果提示,本方法可用以区分耐药和敏感细胞,有希望成为临床个体化疗敏感性预测的重要指标之一。

关键词: 多药耐药基因逆转录多聚酶链反应人白血病细胞株培养的肿瘤细胞    
Abstract:

A highly sensitive,specific assay for measuring the expression of mdr 1 gene in tumor cells,based on the reverse transcription-polymerase chain reaction (RT-PCR),was established.The expression of mdr 1 gene of the drug resistant cell lines K5 62/VCR,K562/DOX,induced by vincristine and doxorubicin respectively,and the sensitive cell line K562 was examined by RT-PCR.It was shown that through 30 cycles of amplification,the mdr 1 product could be detected in the resistant cell lines K562/VCR and K562/DOX,but not in the sensitive cell line K562.The findings suggested that RT-PCR assay could be used to distinguish drug-resistunt cells from sensitive cells and might be considered as one of the important parameters in predicting the sensitivity of anticancer drugs for individual patients clinically.

Key words: Multidrug resistance gene    Reverse transcription-polymerase chain reaction    Human leukemia cell line    Tumor cells, cultured
收稿日期: 1994-08-26 出版日期: 1995-03-25
基金资助:

国家"八五"攻关基金,浙江省自然科学基金

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引用本文:

杨骅, 曹江, 胡汛, 郑树, 董海涛. 用逆转录多聚酶链反应法检测多药耐药基因(mdr 1)的表达[J]. 浙江大学学报(医学版), 1995, 24(2): 49-51.

Yang Hua, Dong Haitao, Cao Jiang, et al. ANALYSIS OF MDR 1 GENE EXPRESSION BY REVERSE TRANSCRIPTION-POL YMERASE CHAIN REACTION. Journal of ZheJiang University(Medical Science), 1995, 24(2): 49-51.

链接本文:

https://www.zjujournals.com/med/CN/10.3785/j.issn.1008-9292.1995.02.001        https://www.zjujournals.com/med/CN/Y1995/V24/I2/49

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