Zhang Kun-Zhong, Xu Jian-Hua, Huang Xiu-Wang, Wu Li-Xian, Su Yu, Chen Yuan-Zhong
Institute of Clinical Pharmacology, School of Pharmacy, Fujian Medical University, Fujian 350004, China.
Acta Pharmacol Sin. 2007 Jan;28(1):105-10. doi: 10.1111/j.1745-7254.2007.00471.x.
To investigate the growth inhibition effect of the combination of bcr/abl phosphorothioate antisense oligonucleotides (PS-ASODN) and curcumin (cur), and the possible mechanisms of cur on the chronic myelogenous leukemia cell line K562.
The K562 cell line was used as a P210( bcr/abl )-positive cell model in vitro and was exposed to different concentrations of PS-ASODN (0-20 micromol/L), cur (0-20 micromol/L), or a combination of both. Growth inhibition and apoptosis of K562 cells were assessed by MTT assay and AO/EB fluorescent staining, respectively. The expression levels of P210( bcr/abl ), NF-kappaB and heat shock protein 90 (Hsp90) were assessed by Western blot.
Exposure to cur (5-20 micromol/L) and PSASODN (5-20 micromol/L) resulted in a synergistic inhibitory effect on cell growth. Growth inhibition was associated with the inhibition of the proliferation and induction of apoptosis. Western blot analysis showed that the drugs synergistically downregulated the level of P210( bcr/abl ) and NF-kappaB. Cur downregulated Hsp90, whereas no synergism was observed when cur was combined with PS-ASODN.
PS-ASODN and cur exhibited a synergistic inhibitory effect on the cell growth of K562. The synergistic growth inhibition was mediated through different mechanisms that involved the inhibition of P210( bcr/abl ).
探讨bcr/abl硫代磷酸反义寡核苷酸(PS-ASODN)与姜黄素(cur)联合应用对慢性髓性白血病细胞系K562的生长抑制作用及cur可能的作用机制。
以K562细胞系作为体外P210(bcr/abl)阳性细胞模型,分别用不同浓度的PS-ASODN(0 - 20 μmol/L)、cur(0 - 20 μmol/L)或两者联合处理。分别采用MTT法和AO/EB荧光染色法评估K562细胞的生长抑制和凋亡情况。采用蛋白质免疫印迹法检测P210(bcr/abl)、核因子κB(NF-κB)和热休克蛋白90(Hsp90)的表达水平。
cur(5 - 20 μmol/L)和PS-ASODN(5 - 20 μmol/L)联合应用对细胞生长具有协同抑制作用。生长抑制与细胞增殖的抑制和凋亡的诱导有关。蛋白质免疫印迹分析显示,两种药物协同下调P210(bcr/abl)和NF-κB的水平。cur下调Hsp90的表达,而cur与PS-ASODN联合应用时未观察到协同作用。
PS-ASODN和cur对K562细胞生长具有协同抑制作用。协同生长抑制是通过不同机制介导的,其中涉及对P210(bcr/abl)的抑制。