Chen H, Luo Z, Luo S
Research Center for Molecular Biology, Hunan Medical University, Changsha 410078, China.
Zhonghua Yi Xue Za Zhi. 2000 Aug;80(8):606-9.
To observe the effect of hydroxyurea (HU) alone and in combination with interferon-alpha (IFN-alpha) on the cell growth and cell death, and the related oncogene expression of chronic myelogenous leukemia (CML) cell line, K562 cells. To further investigate the molecular basis of combination therapy on CML by chemotherapeutants combined with cytokines.
The proliferation and viability of K562 cells were detected by cell-counting and trypan blue dye exclusion test. The levels of bcr-abl, bax and c-myc gene expression in K562 cells incubated for 48 hours were examined using RT-PCR technique.
proliferation was suppressed and cell death process was accelerated by both HU and HU combined with IFN-alpha. HU significantly inhibited bcr-abl gene expression and increased bax gene expression level (both P < 0.05 as compared with that of control). Furthermore, IFN-alpha dose-dependently enhanced the regulatory effects of HU on bcr-abl and bax gene expression. HU alone and in combination with IFN-alpha suppressed slightly c-myc gene expression.
Both HU and HU combined with IFN-alpha can inhibit cell proliferation and promote cell death or apoptotic cell death by regulating the expression levels of the genes relating to cell proliferation and apoptosis. The molecular mechanism of HU and IFN-alpha synergistically acting on leukemic cells is further elucidated from the expression level of the related genes which control the balance of survival and death or apoptosis of the cells.
观察羟基脲(HU)单独及联合α-干扰素(IFN-α)对慢性粒细胞白血病(CML)细胞系K562细胞生长、细胞死亡及相关癌基因表达的影响。进一步探讨化疗药物联合细胞因子治疗CML的分子基础。
采用细胞计数和台盼蓝拒染试验检测K562细胞的增殖和活力。应用逆转录-聚合酶链反应(RT-PCR)技术检测培养48小时的K562细胞中bcr-abl、bax和c-myc基因的表达水平。
HU及HU联合IFN-α均抑制K562细胞增殖并加速细胞死亡进程。HU显著抑制bcr-abl基因表达并提高bax基因表达水平(与对照组相比,均P<0.05)。此外,IFN-α呈剂量依赖性增强HU对bcr-abl和bax基因表达的调控作用。HU单独及联合IFN-α均轻微抑制c-myc基因表达。
HU及HU联合IFN-α均可通过调节细胞增殖和凋亡相关基因的表达水平抑制细胞增殖并促进细胞死亡或凋亡性细胞死亡。从控制细胞生存与死亡或凋亡平衡的相关基因表达水平进一步阐明了HU与IFN-α协同作用于白血病细胞的分子机制。