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多药耐药细胞系K562/HHT和K562/VCR的建立及耐药性逆转的研究 被引量:8

Establishment of multidrug resistant cell lines K562/HHT and K562/VCR and reversal of drug resistance
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摘要 目的研究人白血病细胞多药耐药(MDR)的发生机理及逆转方法。方法建立了K562/HHT和K562/VCR两株MDR细胞系,经免疫组化染色观察了P-糖蛋白(Pgp)和MDR相关蛋白(MRP)的表达;采用四氮甲基唑蓝(MTT)药敏试验及测定细胞内柔红霉素(DNR)含量的方法研究了异搏定和红霉素对MDR的逆转作用。结果两株MDR细胞系均有Pgp高度表达,但无MRP表达。5μg/ml异搏定和50μg/ml红霉素都能部分逆转两株MDR细胞系的耐药性。2.5~10μg/ml异搏定不仅能增加MDR细胞对DNR的摄取量,也能减少DNR的外排,且上述作用随异搏定浓度的增加而增强;50~200μg/ml红霉素则对MDR细胞摄取和外排DNR无明显影响。结论Pgp可能与白血病细胞产生MDR有关;异搏定和红霉素对白血病细胞MDR有逆转作用。 Objective To investigate the mechanism of multidrug resistance (MDR) in human leukemic cells and the way to overcome MDR. Methods The authors established two MDR cell lines K562/HHT and K562/VCR. The expressions of P glycoprotein (Pgp) and MDR related protein (MRP) in the two MDR cell lines were observed by immunohistochemical staining and the reversal of MDR by verapamil and erythromycin was studied by MTT assay or by the determination of the amount of daunorubicin (DNR) in cells. Results The two MDR cell lines overexpressed Pgp but didn′t express MRP. The drug resistance of the two MDR cell lines could be partly reversed by 5 μg/ml of verapamil or 50 μg/ml of erythromycin. 2.5~10 μg/ml of verapamil increased DNR accumulation and retention in the two MDR cell lines, and the effect became obvious along with an increase in verapamil concentration. 50~200 μg/ml of erythromycin, however, did not impact DNR accumulation and retention in the two MDR cell lines. Conclusion Pgp might be in association with the MDR of leukemic cells. Verapamil and erythromycin could reverse the MDR of leukemic cells.
出处 《中华儿科杂志》 CAS CSCD 北大核心 1998年第1期15-18,共4页 Chinese Journal of Pediatrics
关键词 白血病 抗药性 多药 维拉帕米 红霉素 药物疗法 Leukemia Drug resistance, multiple Verapamil Erythromycin
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