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三氧化二砷对多药耐药白血病细胞株K562/A02中血管内皮生长因子及P-糖蛋白表达的影响

[Effects of arsenic trioxide on expressions of vascular endothelial growth factor and P-glycoprotein in multidrug resistant leukemia cell line K562/A02].

作者信息

Liang Hong, Zhang Yu, Zhang Jian-dong, Gu Jian, Ma Li, Wang Xiao-ling, Shen Wei-gan

机构信息

Medical College, Yangzhou University, Yangzhou, Jiangsu Province 225001, China.

出版信息

Zhong Xi Yi Jie He Xue Bao. 2007 Nov;5(6):647-50. doi: 10.3736/jcim20070609.

Abstract

OBJECTIVE

To investigate the effects of arsenic trioxide (ATO) on the expressions of vascular endothelial growth factor (VEGF) and P-glycoprotein (P-gp) in K562/A02 cells and to explore the correlation between VEGF and P-gp.

METHODS

The inhibition rate of K562/A02 cell proliferation was detected by using methyl thiazolyl tetrazolium assay (MTT); the level of VEGF was detected by enzyme-linked immunosorbent assay (ELISA) and the expression rate of P-gp was determined by flow cytometry (FCM).

RESULTS

0.05 micromol/L ATO had no influences on the cell proliferation and the expression of VEGF in K562/A02 cells; 0.4 and 3.2 micromol/L ATO could significantly inhibit the K562/A02 cell proliferation and down-regulate the expression of VEGF in K562/A02 cells (P<0.05). The expression of P-gp did not changed after being exposed to 0.05 and 0.4 micromol/L ATO for 24, 48 and 72 hours (P>0.05). 3.2 micromol/L ATO could remarkably reduce the expression of P-gp in K562/A02 cells after 48- and 72-hour incubation with ATO (P<0.05).

CONCLUSIONS

The down-regulation of P-gp and VEGF after being exposed to ATO probably contributes to the reversion of multidrug resistance in K562/A02 cells. The level of VEGF may be related to the expression rate of P-gp in K562/A02 cells.

摘要

目的

研究三氧化二砷(ATO)对K562/A02细胞中血管内皮生长因子(VEGF)和P-糖蛋白(P-gp)表达的影响,并探讨VEGF与P-gp之间的相关性。

方法

采用甲基噻唑基四氮唑蓝比色法(MTT)检测K562/A02细胞增殖抑制率;采用酶联免疫吸附测定法(ELISA)检测VEGF水平,采用流式细胞术(FCM)测定P-gp表达率。

结果

0.05 μmol/L ATO对K562/A02细胞增殖及VEGF表达无影响;0.4和3.2 μmol/L ATO可显著抑制K562/A02细胞增殖,并下调K562/A02细胞中VEGF的表达(P<0.05)。在0.05和0.4 μmol/L ATO作用24、48和72小时后,P-gp的表达未发生变化(P>0.05)。在与3.2 μmol/L ATO孵育48和72小时后,K562/A02细胞中P-gp的表达显著降低(P<0.05)。

结论

ATO作用后P-gp和VEGF的下调可能有助于K562/A02细胞多药耐药性的逆转。VEGF水平可能与K562/A02细胞中P-gp的表达率有关。

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