期刊文献+

microRNA-15家族功能研究进展 被引量:6

Cellular function of microRNA-15 family
原文传递
导出
摘要 微小RNA(microRNAs,miRNAs)是一类具有转录后调节作用的短小的内源性非编码RNA,其中miR-15家族参与凋亡、细胞分化与周期调控、应激等重要细胞功能活动的调节,并与多种人类疾病如肿瘤、心血管疾病、神经退行性疾病等相关,具有潜在的治疗前景及干预价值。本文就miR-15家族的重要功能及治疗应用前景作一综述。 microRNAs (miRNAs) are non-coding endogenous short RNAs which are involved in regulating gene expression at the post-transcriptional level. miR-15 family is increasingly found to play great roles in important cell processes, such as apoptosis, cell differentiation and stress response. Growing evidence indicates that miR-15 family members are implicated in tumor, cardiovascular disease and neurodegenerative disease. miRNAs have emerged as a new promising subset of therapeutic targets. The present paper reviewed the important function of miR-15 family and new approaches for miRNA-based therapy.
作者 刘丽凤 王禹
出处 《生理学报》 CAS CSCD 北大核心 2012年第1期101-106,共6页 Acta Physiologica Sinica
关键词 微小RNA miR-15家族 凋亡 肿瘤 心血管疾病 microRNAs miR-15 family apoptosis neoplasm cardiovascular disease
  • 相关文献

参考文献32

  • 1Bartel DP.MicroRNAs:genomics,biogenesis,mechanism,and function.Cell2004;116(2):281–297.
  • 2Bartel DP.MicroRNAs:target recognition and regulatory functions.Cell2009;136(2):215–233.
  • 3Axtell MJ,Westholm JO,Lai EC.Vive la difference:biogen-esis and evolution of microRNAs in plants and animals.Ge-nome Biol2011;12(4):221.
  • 4Okamura K,Hagen JW,Duan H,Tyler DM,Lai EC.The mirtron pathway generates microRNA-class regulatory RNAs in Drosophila.Cell2007;130(1):89–100.
  • 5Park JE,Heo I,Tian Y,Simanshu DK,Chang H,Jee D,Patel DJ,KimVN.Dicerrecognizesthe5’endofRNAforeffi-cient and accurate processing.Nature2011;475(7355):201–205.
  • 6Zhang X,Zeng Y.The terminal loop region controls microR-NA processing by Drosha and Dicer.Nucleic Acids Res2010;38(21):7689–7697.
  • 7Lewis BP,Burge CB,Bartel DP.Conserved seed pairing,of-tenflankedbyadenosines,indicatesthatthousandsofhuman genes are microRNA targets.Cell2005;120(1):15–20.
  • 8Bargaje R,Hariharan M,Scaria V,Pillai B.Consensus miR-NAexpressionprofilesderivedfrominterplatformnormal-ization of microarray data.RNA2010;16(1):16–25.
  • 9Yue J,Tigyi G.Conservation of miR-15a/16-1and miR-15b/16-2clusters.Mamm Genome2010;21(1–2):88–94.
  • 10Qu KZ,Zhang K,Li H,Afdhal NH,Albitar M.Circulating microRNAs as biomarkers for hepatocellular carcinoma.J Clin Gastroenterol2011;45(4):355–360.

同被引文献74

  • 1Garzon R, Calin GA, Croce CM, MicroRNAs in Cancer[J]. Annu Rev Meal,2009,60:167-179.
  • 2Barrel DP. MicroRNAs.. Genomics, biogenesis, mechanism and function[J]. Cell, 2004,116(2) .. 281-297.
  • 3Chen C, Ridzon DA, Broomer A J, et al. Real-time quantification of microRNAs by stem-loop RT-PCR[J].NucleicAcids Res, 2005,33(20) :e179.
  • 4Thomson JM, Newman M, Parker JS, et ol. Extensive post- transcriptional regulation of microRNAs and its implications for cancer[J]. Genes Dev, 2006,20(16): 2202-2207.
  • 5Yingqing S, Seongjoon K, Neill W, et al. Development of a micro-array to detect human and mouse microRNAs and characterization of expression in human organs[JJ.Nucleic Acids Res, 2004,32(22): 2486-2494.
  • 6Caifu C, Kelly M, Ada HW, et al. Real-time PCR: Advancing RNA Interference and MicroRNA Studies[J].Nucleic Acids Research, 2004,32, (22): el 88.
  • 7Finnerty JR, Wang WX, Hebert SS, et al. The miR-15/107 group of microRNA genes: evolutionary biology, cellular functions, and roles in human diseases[JJ.J Mol Biol,2010,402(3): 491-509.
  • 8He JF, Luo YM, Wan XFI, et al. Biogenesis of miRNA-195 and its role in biogenesis, the cell cycle, and apoptosis [ J ]. J Biochem Mol Toxicology, 2011,25(6) :404-408.
  • 9Luo Q, Wei C, Li X, et al. MicroRNA-195-5p is a potential diagnostic and therapeutic target for breast cancer [ J ]. Oncol Rep, 2014,31 (3) :1096-1102.
  • 10Xu T, Zhu Y, Xiong Y, et al. MicroRNA-195 suppresses tu- morigenicity and regulates GI/S transition of human hepatocellu- lar carcinoma cells [ J ]. Hepatology, 2009,50 ( 1 ) : 113 -121.

引证文献6

二级引证文献11

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