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作 者:张春平[1] 代洪生 王津迪 潘光敏 高志星[2] 季万胜[2] ZHANG Chunping;DAI Hongsheng;WANG Jindi;Pan Guangmin;GAO Zhixing;JI Wansheng(Weifang Medical College,Weifang 261053,China;Department of Gastroenterology;Hospital Affiliated to Weifang Medical University,Weifang 261031,China)
机构地区:[1]潍坊医学院,山东潍坊261053 [2]潍坊医学院附属医院消化内科,山东潍坊261031
出 处:《现代医学》2018年第7期748-750,共3页Modern Medical Journal
基 金:山东省优秀中青年科学家科研奖励基金资助项目(BS2010SW034)
摘 要:目的:探讨重组改构人肿瘤坏死因子-α(rmhTNF-α)抑制人胃癌细胞增殖的作用机制。方法:将不同浓度(0、50、100、200 U·ml^(-1))的rmhTNF-α作用于人胃癌细胞系MKN45(干预组),采用增殖/毒性检测试剂(CCK-8)测定细胞抑制率,实时荧光定量PCR测定Δ133p53、cjun、cfos mRNA表达变化。结果:细胞抑制率干预组高于对照组(rmhTNF-α0 U·ml^(-1)组),且随rmhTNF-α浓度的增加而增高(P<0.05);Δ133p53mRNA表达干预组较对照组低,且随rmhTNF-α浓度的增加而降低(P<0.05),cjun、cfos mRNA表达干预组较对照组高,且随rmhTNF-α浓度的增加而增高(均P<0.05)。Pearson相关分析显示,Δ133p53 mRNA与cjun和cfos mRNA的表达呈显著负相关(分别r=-0.954、-0.947,均P<0.01)。结论:rmhTNF-α可能是通过抑制Δ133p53表达并促进cjun、cfos表达而抑制胃癌细胞的增殖,其对Δ133p53的抑制作用可能是cjun、cfos介导的。Objective: To investigate the mechanism of recombinant mutant human tumor necrosis factor-α(rmhTNF-α) inhibit the proliferation of human gastric cancer cell. Methods: Human gastric cancer cell lines MKN45 were treated with different concentrations(0,50,100,200 U·ml^-1) of rmhTNF-α intervention group. The cell inhibition rate was detected by proliferation/toxicity detection kit(CCK-8),and the expression of Δ133 p53,cjun,cfos mRNA were detected by real-time fluorescent quantitative reverse transcription polymerase chain reaction. Results: The cell inhibition rates in the intervention group was higher than that in the control group(rmhTNF-α 0 U·ml^-1 group) and it increased with the increasing of concentration of rmhTNF-α(P〈0. 05); the expression of Δ133 p53 mRNA in the intervention group was lower than that in the control group and it decreased with the increasing of concentration of rmhTNF-α(P〈0. 05); the expression of cjun,cfos mRNA in the intervention group were higher than those in the control group and they increased with the increasing of concentration of rmhTNF-α(all P〈0. 05). Pearson correclation analysis showed the expression was negatively correlated markedly betweenΔ133 p53 mRNA and cjun,cfos mRNA(r =-0. 954,-0. 947,respectivly,all P〈0. 01). Conclusion: rmhTNF may inhibit Δ133 p53 expression and promote cjun,cfos expression to further inhibit gastric cancer cell proliferation,the inhibitory effect on Δ133 p53 may mediated by cjun and cfos.
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