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红系分化因子(激活素A)对多药耐药的人K562红白血病细胞中P-糖蛋白表达的抑制作用。

Inhibition by erythroid differentiation factor (activin A) of P-glycoprotein expression in multidrug-resistant human K562 erythroleukemia cells.

作者信息

Okabe-Kado J, Hayashi M, Honma Y, Hozumi M, Tsuruo T

机构信息

Department of Chemotherapy, Saitama Cancer Center Research Institute, Japan.

出版信息

Cancer Res. 1991 May 15;51(10):2582-6.

PMID:1673636
Abstract

The K562/VCR cell line, exhibiting acquired multidrug resistance (MDR) with increased expression of a cell surface glycoprotein (P-glycoprotein), was isolated from human erythroleukemia K562 cells. Various compounds that induced erythroid differentiation of K562 cells were tested for their effects on growth and differentiation of these K562/VCR cells. Sodium butyrate, hemin, 1-beta-D-arabinofuranosylcytosine, and erythroid differentiation factor (EDF) induced erythroid differentiation of K562/VCR cells as well as K562 cells. The MDR of K562/VCR cells was partly overcome by treatment with EDF but not with the other inducers. Expression of P-glycoprotein by K562/VCR cells was measured by radioimmunoassay using MRK16 monoclonal antibody. Results showed that EDF caused down-regulation of P-glycoprotein in K562/VCR cells, whereas the other inducers did not cause its down-regulation. Thus, in addition to inducing erythroid differentiation, EDF enhanced the sensitivity of K562/VCR cells to multidrugs and suppressed expression of P-glycoprotein. These results suggest that differentiation inducers may be useful in chemotherapy of leukemic MDR cells.

摘要

K562/VCR细胞系是从人红白血病K562细胞中分离出来的,它表现出获得性多药耐药(MDR),细胞表面糖蛋白(P-糖蛋白)的表达增加。测试了各种诱导K562细胞红系分化的化合物对这些K562/VCR细胞生长和分化的影响。丁酸钠、血红素、1-β-D-阿拉伯呋喃糖基胞嘧啶和红系分化因子(EDF)可诱导K562/VCR细胞以及K562细胞的红系分化。EDF处理可部分克服K562/VCR细胞的MDR,而其他诱导剂则不能。使用MRK16单克隆抗体通过放射免疫测定法测量K562/VCR细胞中P-糖蛋白的表达。结果表明,EDF导致K562/VCR细胞中P-糖蛋白的下调,而其他诱导剂则不会导致其下调。因此,EDF除了诱导红系分化外,还增强了K562/VCR细胞对多种药物的敏感性,并抑制了P-糖蛋白的表达。这些结果表明,分化诱导剂可能对白血病MDR细胞的化疗有用。

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