期刊文献+

血清miR-21及AFP在大鼠肝癌发生过程中的动态表达比较分析 被引量:4

A Comparison Analysis between the Dynamic Expressions of Serum miR-21 and AFP During the Process of Liver Cancer Development in Rats
原文传递
导出
摘要 目的:分析血清miR-21在肝癌发生过程中的表达水平并将其与传统肝癌血清标志物甲胎蛋白(AFP)比较,探索其成为肝癌早期诊断血清标志物的可能性。方法:二乙基亚硝胺(DENA)腹腔注射诱导建立大鼠肝癌模型,建模过程中收集造癌各个阶段的血清。Realtime-PCR检测血清miR-21的表达情况,ELISA法检测血清AFP水平。结果:与正常组及纤维化期大鼠相比,miR-21在肝硬化期、肝癌早期、肝癌晚期的大鼠血清均有不同程度上调(P<0.05),AFP在肝癌早、晚期的大鼠血清明显上调(P<0.05);与肝硬化期大鼠比较,肝癌早、晚期大鼠体内的miR-21表达显著上调(P<0.05),AFP在肝癌早期、肝癌晚期均显著上调(P<0.05)。结论:血清miR-21参与了肝癌发生的过程,对于肝癌发生的各个阶段均有很大的指示作用,可能作为肝癌预防和早期诊断的一个潜在标志物。 Objective: To investigate whether serum microRNA-21 (miR:21) could be used as a novel biomarker of liver cancer by comparing with serum AFP. Methods: Diethylnirtosamine (DENA) abdominal injection was applied to induce liver cancer in F344 rats. Blood samples of rats were collected for analysis. Real-time quantitative PCR technique and ELISA test were used respectively to measure the expressions of serum miR-21 and AFP during the liver cancer developing process. Results: Comparing with that in normal rats and liver fibrosis rats, miR-21 had higher expressions in liver cirrhosis rats, early liver cancer rats and advanced liver cancer rats (P〈0.05), while AFP had higher expressions only in early and advanced liver cancer rats (P〈0.05). During the developmental process of liver cancer, the miR-21 expression kept on increasing, while the AFP expression only increased at the stage of tumor formation. Conclusion: Data indicated that MiR-21 played an important role in liver cancer development and had diagnostic value for indicating early liver cancer.
出处 《现代生物医学进展》 CAS 2012年第12期2282-2284,2297,共4页 Progress in Modern Biomedicine
基金 国家自然科学基金项目(81030010 81170419)
关键词 肝癌 血清 MIR-21 AFP 早期诊断 Hepatocellular carcinoma Serum Early diagnosis MiR-21 AFP
  • 相关文献

参考文献4

二级参考文献40

共引文献45

同被引文献39

  • 1Hassan El-Garem,Ayman Ammer,Hany Shehab,Olfat Shaker,Mohammed Anwer,Wafaa El-Akel,Heba Omar.Circulating micro RNA, mi R-122 and mi R-221 signature in Egyptian patients with chronic hepatitis C related hepatocellular carcinoma[J].World Journal of Hepatology,2014,6(11):818-824. 被引量:18
  • 2Silahtaroglu A, Stenvang J. MicroRNAs, epigenetics and disease [J].Essays Biochem,2010,48( 1):165-185.
  • 3Mayr M,Zampetaki A, Willeit P, et al. MicroRNAs within thecontinuum of postgenomics biomarker discovery [J]. ArteriosclerThromb Vase Biol,2013,33(2):206-214.
  • 4Somel M, Liu X,Khaitovich P. Human brain evolution: transcripts,metabolites and their regulators [J]. Nat Rev Neurosci,2013,14(2): 112-127.
  • 5Nana-Sinkam SP,Croce CM. Clinical applications for microRNAs incancer[J]. Clin Pharmacol Ther,2013,93( 1):98-104.
  • 6Ross SA, Davis CD. MicroRNA, Nutrition, and Cancer Prevention [J].Adv Nutr,2011,2(6):472-485.
  • 7Zhang Y, Wu JH, Han F, et al. Arsenic trioxide induced apoptosis inretinoblastoma cells by abnormal expression of microRNA-376a [J].Neoplasma,2013,60(3):247-53.
  • 8Shen J, Stass SA, Jiang F. MicroRNAs as potential biomarkers inhuman solid tumors[J]. Cancer Lett,2013,329(2): 125-136.
  • 9Lee RC, Feinbaum RL, Ambros V. The C. elegans heterochronicgene lin-4 encodes small RNAs with antisense complementarity tolin-14[J]. Cell,1993,75(5):843-854.
  • 10Hu J, Wang Z,Tan CJ, et al. Plasma microma, a potential biomarkerfor acute rejection after liver transplantation [J]. Transplantation,2013Mar 4[Epub ahead of print].

引证文献4

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部