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作 者:于鑫[1] 卢发强[1] 宗成国[1] 张卫军[1] 牟锐[1] 魏丹冰 范世珍 于波海 YU Xin;LU Fa-qiang;ZONG Cheng-guo(Clinical Laboratory,Affiliated Zhongshan Hospital of Daian University,Dalian 116001,China)
机构地区:[1]大连大学附属中山医院检验科,辽宁大连116001 [2]广州中医药大学深圳医院
出 处:《中国实验诊断学》2019年第11期1965-1969,共5页Chinese Journal of Laboratory Diagnosis
基 金:大连市医学科学研究计划项目(No.1611115);黑龙江省自然科学基金项目(No.H2018055);广东省中医药局科研项目(No.20191293);深圳市福田区卫生公益性科研项目(NO.FTWS2018068)
摘 要:目的研究姜黄素诱导自噬对K562细胞增殖的作用。方法采用MTT法检测不同浓度的姜黄素及自噬特异性抑制剂3-MA对K562细胞存活率的影响;通过Western blot法检测自噬标志蛋白Beclin1及LC3-Ⅱ/LC3-Ⅰ的水平评价自噬;应用实时定量PCR法检测BCR-ABL融合基因的表达。结果姜黄素以剂量、时间依赖方式抑制K562细胞增殖;与加入3-MA的对照组相比,Beclin1的水平及LC3-Ⅱ/LC3-Ⅰ的比值明显升高;姜黄素可导致BCRABL融合基因的水平降低。结论姜黄素诱导自噬可抑制K562细胞增殖并下调BCR-ABL融合基因的表达水平。Objective To investigate the proliferative effect of curcumin-induced autophagy on chronic myelogenous leukemia cell line K562.Methods K562cells was incubated with various concentrations of curcumin and autophagyspecific inhibitor 3-MA,the cell viability was measured by MTT;the level of autophagy marker protein Beclin1and the ratio of LC3-Ⅱ/LC3-Ⅰwere detected by Western blot to evaluate autophagy;mRNA expression level of BCR-ABL fusion gene was determined by quantitative real-time PCR.Results Dose-and time-dependent K562cell viability inhibition was observed following curcumin treatment;the level of Beclin1and the ratio of LC3-Ⅱ/LC3-Ⅰwere significantly increased compared with the control group with 3-MA;in addition,curcumin reduced the level of BCR-ABL fusion gene.Conclusion Curcumin could induce autophagy to inhibit the proliferation of K562cells and downregulate expression level of BCR-ABL fusion gene.
关 键 词:姜黄素 自噬 慢性粒细胞白血病 K562细胞 BCR-ABL融合基因
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