The role of Src kinase inhibitor ZD6474 on multi-drug resistant K562/A02 cells.
- Author:
Hong-yun JIA
1
;
Juan LI
;
Zhong-ying WANG
;
Qiang ZHOU
;
Xiao-man WU
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Apoptosis; drug effects; Cell Cycle; drug effects; Cell Proliferation; drug effects; Drug Resistance, Multiple; drug effects; Drug Resistance, Neoplasm; drug effects; Female; Humans; K562 Cells; Mice; Mice, Inbred BALB C; Piperidines; pharmacology; Quinazolines; pharmacology; src-Family Kinases; antagonists & inhibitors
- From: Chinese Journal of Hematology 2012;33(3):220-224
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the role of Src kinase inhibitor ZD6474 on the growth of multidrug-resistant K562/A02 cells and its regulatory mechanisms.
METHODSThe possible mechanisms of drug-resistance were tested by Western blot. Proliferation assays and cell cycle distribution were analyzed by WST metric analysis. Western blot were used to investigate the mechanisms of antiproliferative activity induced by tyrosine kinase inhibitor ZD6474. The in vivo anti-tumor activity was evaluated in K562, K562/A02 xenografted nude mice by administration of ZD6474 (25 - 100 mg×kg(-1)×d(-1), PO).
RESULTSCompared with parental K562 cells, marked high levels of p-Src and Src expression were detected in K562/A02 cells. WST results showed that the IC(50) values of ZD6474 on K562 and K562/A02 after 48 hours incubation were (1.61 ± 0.07) µmol/L and (3.22 ± 0.21)µmol/L, respectively. ZD6474 caused an accumulation of cells in the G(0)/G(1) fraction and apoptosis by inhibiting the expressions of p-Src and Src kinase. Administration of ZD6474 produced a dose-dependent inhibition of tumor growth. 50 mg/kg ZD6474 produced the growth inhibition rates of 43.7% and 56.3%, respectively in K562 and K562/A02.
CONCLUSIONOur results indicated that inhibiting Src kinase could induce K562/A02 cells apoptosis in vitro and in vivo.
