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ABCB5和MDR1对急性髓系白血病耐药的影响

李真真 张晓龙 杨雨琪 张晴 袁向飞 范冬梅

中国药理学通报Issue(9):1214-1218,1219,6.
中国药理学通报Issue(9):1214-1218,1219,6.DOI:10.3969/j.issn.1001-1978.2014.09.008

ABCB5和MDR1对急性髓系白血病耐药的影响

Effect evaluation of ABCB5 and MDR1 on multidrug resistance in acute myeloid leukemia

李真真 1张晓龙 1杨雨琪 2张晴 1袁向飞 1范冬梅1

作者信息

  • 1. 中国医学科学院·北京协和医学院血液病医院血液学研究所,实验血液学国家重点实验室,天津 300020
  • 2. 天津医科大学药学院,天津 300070
  • 折叠

摘要

Abstract

Aim To investigate the expression of AB-CB5 and MDR1 in the cell line KG1 a and samples from acute myeloid leukemia ( AML) and their effects on multidrug resistance. Methods The expression of ABCB5 and P-gp ( the expressed product of MDR1 ) in KG1 a cells were detected by flow cytometry as well as Western blot analysis; KG1 a cells were transfected with the specific siRNA of ABCB5 using lipo2000 to reduce the expression of ABCB5; intracellular rhoda-mine123 was measured by flow cytometry;cell viability was detected by MTT; the expressions of ABCB5 and MDR1 in samples from AML were detected by real time PCR. Results ABCB5 and P-gp were overexpressed in KG1 a;the specific siRNA of ABCB5 transiently in-hibited the expression of ABCB5 in KG1 a; the siAB-CB5-KG1 a cells increased the intracellular rhodamine 123 and have been more sensitive to adriamycin com-pared with the parent KG1a. ABCB5 gene expression in samples from AML was higher than healthy people. Further, the expression of ABCB5 in 38 relapse or re-fractory AML significantly exceeded the 33 drug sensi-tive. And we found a significant positive correlation between ABCB5 expression and MDR1 gene expression in the 38 patients with relapse or refractory AML. Conclusion ABCB5 , as well as P-gp contributes to mediate multidrug resistance of AML, which provides a novel target for the therapy of relapse or refractory AML.

关键词

ABCB5/P-gp/急性髓系白血病/siABCB5/多药耐药/复发难治

Key words

ABCB5/P-gp/AML/siABCB5/MDR/relapse/refractory

分类

医药卫生

引用本文复制引用

李真真,张晓龙,杨雨琪,张晴,袁向飞,范冬梅..ABCB5和MDR1对急性髓系白血病耐药的影响[J].中国药理学通报,2014,(9):1214-1218,1219,6.

基金项目

国家自然科学基金资助项目(No 30971291) (No 30971291)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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