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作 者:刘黎琼[1] 李慧玉[1] 曾惠[2] 刘隽[1] 周咏明[1] 黄士昂[1]
机构地区:[1]华中科技大学同济医学院附属协和医院干细胞研究与应用中心,武汉430022 [2]浙江省嘉兴市第一医院
出 处:《临床血液学杂志》2008年第3期247-249,254,共4页Journal of Clinical Hematology
基 金:国家重点研究项目(No:001CB510103);国家杰出青年基金资助项目(No:30225038)
摘 要:目的:研究herg1基因在慢性髓细胞白血病(CML)细胞的表达及其对CML细胞增殖和细胞周期的调控作用。方法:应用RT-PCR方法测定33例初治慢性髓细胞白血病患者和10例健康志愿者的骨髓细胞herg1基因的表达,检测特异性抑制剂处理后CML细胞株K562增殖凋亡和细胞周期的变化。结果:①在初发CML病例中,herg1mRNA的表达率是72.7%(24/33),高于正常对照(20%)(P<0.01)。CML加速期和急变期的herg1mRNA的表达率分别为75%和90.9%,高于正常对照(P<0.01),但是herg1的表达与CML的临床分期并无相关性(P>0.05)。②E-4031(1μmol/L)可呈时间依赖性抑制细胞增殖,不诱导明显凋亡。③E-4031阻滞K562细胞周期于G1期。结论:CML细胞herg1基因表达失调,IHERG抑制剂E-4031对K562细胞的增殖和细胞周期具有调控作用,herg1基因可能与CML发病机制相关。Objective: To investigate the mRNA expression of hergl in chronic myeloid leukemia (CML) patients and to investigate the effects of IHERC; inhibitor E-4031 on the proliferation and apoptosis of human leukemia cell line (K562) . Method:The expression of myeloid cell hergl gene in 33 de novo CML patients and 10 normal control (NC) was detected by transcription polymerase chain reaction (RT-PCR). The effects of E-4031 on the proliferation of K562 leukemia cells were assayed by MTT method, cell apoptosis and cell cycle by flow cytometry (FCM). Result:①In the de novo CML cases, the expression rate of hergl mRNA was 72.7% ( 24/33 ), which was higher than NC (20%) (P〈0.01). The expression of hergl in CML-AP(90.9%) and CML-BC (75%) patients was higher than that in NC (P%0.01), but no correlation between hergl expression and clinical staging of chronic myeloid leukemia (P〉0.05). ②With E-4031 (1 μmol/ L) , the inhibitory of proliferation could be observed in a time-dependent manner without more apoptsis. ③E-4031 inhibited K562 cell cycle progression at the G1 phase. Conclusion: The overexpression of hergl gene has been confirmed for the first time in patients with chronic myeloid leukemia. IHERG inhibitor E-4031 inhibited the proliferation of CML cell line K562 partly via cell cycle arrest, hergl gene is related to the pathogenesis of CML.
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