期刊文献+

癌症相关microRNA与靶基因的生物信息学分析 被引量:25

Bioinformatic analysis of cancer-related microRNAs and their target genes
在线阅读 下载PDF
导出
摘要 Micro RNAs(mi RNAs)是一类长度约为22nt的内源性非编码RNA,通过与靶基因转录本互补结合调控基因的表达。近年来,研究发现mi RNA与癌症发生密切相关,mi RNA可以直接充当癌基因或者抑癌基因而影响肿瘤的发生和生长。为更进一步揭示癌症相关mi RNA的特征及靶基因的功能,文章通过数据库搜索及文献检索,在人类基因组中发现了475个癌症相关mi RNA,系统地比较了癌症相关mi RNA与非癌症mi RNA以及基因内和基因间区癌症相关mi RNA在保守性、SNP位点分布、癌谱及转录调控等特性。研究发现,癌症相关mi RNA比非癌症mi RNA保守性要强,发生SNP概率比较低,同时发现mi RNA所涉及癌症数目与保守性成正相关。基因组定位分析发现,癌症相关mi RNA比非癌症mi RNA更倾向于成簇存在。进一步对宿主基因、癌症相关mi RNA及作用的靶基因与癌症发生进行关联分析,发现一些非癌症mi RNA的宿主基因倾向于被癌症mi RNA作用。本研究结果为深入理解mi RNA与癌症之间的关系,以及进一步为mi RNA作为癌症诊断指示物提供理论依据。 MicroRNAs (miRNAs) are a class of --22 nucleotide endogenous noncoding RNAs which regulate gene expression by targeting complementary transcripts. Recent studies have found that miRNAs are closely related to tumorigenesis and can act as oncogenes or tumor suppressor genes to influence the occurrence and development of tumor. To further reveal characteristics of cancer-related miRNAs and the functions of miRNA targets, we obtained 475 miRNAs involved in cancer through database searching and information retrieval. We systematically analyzed and compared thefeatures including conservation, SNP distribution, cancer spectrum width, and transcriptional regulation between cancer and non-cancer related miRNAs as well as between intergenic and intragenic miRNAs. Our results showed that cancer-related miRNAs have higher conservation and lower SNP frequency compared to non-cancer-related miRNAs, and the cancer spectrum of one miRNA is positively correlated with its conservation. Genome analysis showed that cancer-related miRNAs tend to present as clusters compared with non-cancer-related miRNAs. Further association analysis between cancer progression and host genes, cancer-related miRNAs or target genes found that the host genes of some non-cancer related miRNAs tend to be targeted by cancer-related miRNAs. This study provides theoretical basis for further understanding the relationship between miRNA and cancer progression as well as the miRNA-based cancer diagnosis.
出处 《遗传》 CAS CSCD 北大核心 2015年第9期855-864,共10页 Hereditas(Beijing)
基金 南京师范大学泰州学院青年项目(编号:Q201206)资助
关键词 MicroRNAs(miRNAs) 癌症 靶基因 宿主基因 生物信息学 microRNAs (miRNAs) cancer target gene host gene bioinformatics
  • 相关文献

参考文献40

  • 1Lee Y, Kim M, Han JJ, Yeom KH, Lee S, Back SH, Kim VN. MicroRNA genes are transcribed by RNA polymerase II. EMBO J, 2004, 23(20): 4051-4060.
  • 2Lee RC, Feinbaum RL, Ambros V. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell, 1993, 75(5): 843-854.
  • 3Wightman B, Ha I, Ruvkun G. Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans. Cell, 1993, 75(5): 855-862.
  • 4Ambros V, Barrel B, Barrel DP, Burge CB, Carrington JC, Chen XM, Dreyfuss G, Eddy SR, Griffiths-Jones S, Marshall M, Matzke M, Ruvkun G, Tuschl T. A uniform system for microRNA annotation. RNA, 2003, 9(3): 277-279.
  • 5Bushati N, Cohen SM. microRNA functions. Annu Rev Cell Dev Biol, 2007, 23: 175-205.
  • 6Sun BK, Tsao H. Small RNAs in development and disease. JAm AcadDermatol, 2008, 59(5): 725-737.
  • 7Brase JC, Wuttig D, Kuner R, Sfiltmann H. Serum microRNAs as non-invasive biomarkers for cancer. Mol Cancer, 2010, 9(1): 306.
  • 8Cortez MA, Calin GA. MicroRNA identification in plasma and serum: a new tool to diagnose and monitor diseases. Expert Opin Biol Ther, 2009, 9(6): 703-711.
  • 9Kozomara A, Griffiths-Jones S. miRBase: integrating microRNA annotation and deep-sequencing data. Nucleic Acids Res, 2011, 39(Database issue): D 152-D 157.
  • 10Griffiths-Jones S, Saini HK, van Dongen S, Enright AJ. miRBase: tools for microRNA genomics. Nucleic Acids Res, 2008, 36(Database issue): D154-D158.

二级参考文献94

  • 1盛熙晖,杜立新.MicroRNA及其在人和动物上的研究进展[J].遗传,2007,29(6):651-658. 被引量:20
  • 2[1]Horvitz H R,Sulston J E.Isolation and genetic characterization of cell- lineage mutants of the nematode Caenorhabditis ele gans.Genetics,1980,96:435 ~ 454.
  • 3[2]Lee R C,Feinbaum R L,Ambros V.The C.elegans hetero chronic gene lin- 4 encodes small RNAs with antisense com plementarity to lin- 14 RNA.Cell,1993,75:843 ~ 854.
  • 4[3]Wightman B,Ha I,Ruvkun G.Posttranscriptional regulation of the heterochronic gene lin-4 by lin-4 mediates temporal pat tern formation in C.elegans.Cell,1993,75:855~862.
  • 5[4]Moss E G,Lee R C,Ambros V.The cold shock domain protein LIN-28 controls developmental timing in C.elegans and is regulated by lin-4 RNA.Cell,1997,88:637~646.
  • 6[5]Brenda J Reinhart,Frank J Slack,Michael Basson,Amy E Pas quinelli,Jill C Bettinger,Ann E Rougvie,H Robert Horvitz,Gary Ruvkun.The 21 - nucleotide let- 7 RNA regulates de velopmental timing in Caenorhabditis elegans.Nature,2000,403:901~906.
  • 7[6]Amy E Pasquinelli,Brenda J Reinhart,Frank Slack,Mark Q Martindale,Mitzi I Kuroda,Betsy Maller,David C Hayward,Eldon E Ball,Bernard Degnan,Peter M,Spring,Ashok Sriniva san,Mark Fishman,John Finnerty,Joseph Corbo,Michael Le vine,Patrick Leahy,Eric Davidson,Gary Ruvkun.Conservation of sequence and temporal expression of let-7 heterochronic reg ulatory RNA.Nature,2000,408:86 ~ 89.
  • 8[7]Lagos-Quinana M,Rauhut R,Lendeckel W,Tuschl T.Identifi cation of novel genes coding for small expressed RNAs.Sci ence,2001,294:853 ~ 858.
  • 9[8]Lau N C,Lim L P,Weinstein E G,Bartel D P.An abundant class of tiny RNAs with probable regulatory roles in Cae norhabditis elegans.Science,2001,294:858~862.
  • 10[9]Lee R C,Ambros V.An extensive class of small RNAs in Cae norhabditis elegans.Science,2001,294:862 ~ 864.

共引文献35

同被引文献139

  • 1王煜,雷霆,牛洪泉,董震,董芳永,柳再明,薛德麟.树突状细胞瘤内注射和化疗联合治疗脑胶质瘤的实验研究[J].中华神经外科杂志,2006,22(3):184-186. 被引量:11
  • 2张跃萍,何孝华.慷舒灵凝胶在糖尿病足溃疡换药中的应用及护理[J].实用医院临床杂志,2007,4(6):116-116. 被引量:11
  • 3LANDI D, MORENO V, GUINO E, et al. Polymorphisms affecting micro-RNA regulation and associated with the risk of dietary-related cancers: a review from the literature and new evidence for a functional role of rs17281995 (CD86) and rs1051690 (INSR), previously associated with colorectal cancer[J]. Mutat Res,2011,717 (1-2):109-115.
  • 4LIU N, TANG L L, SUN Y, et al. MiR-29c suppresses invasion and metastasis by targeting TIAM1 in nasopharyngeal carcinoma[J]. Cancer Lett,2013,329(2): 181 - 188.
  • 5LIU L, YE J X, QIN Y Z, et al. Evaluation of miR-29c, miR- 124, miR-135a and miR-148a in predicting lymph node metastasis and tumor stage of gastric cancer[J]. Int J Clin Exp Med,2015,8(12): 22227-22236.
  • 6CRISTOBAL I, MADOZ-GURPIDE J, MANSO R, et al. MiR-29c downregulation contributes to metastatic progression in colorectal cancer[J]. Ann Oncol,2015,26(10):2199-2200.
  • 7YU Y, WANG Y, NIU Y, et al. Leukemia inhibitory factor attenuates renal fibrosis through Stat3-miR-29c[J]. Am J Physiol Renal Physiol, 2015,309(7):595-603.
  • 8NONAKA R, MIYAKE Y, HATA T, et al. Circulating miR-103 and miR-720 as novel serum biomarkers for patients with colorectal cancer[J]. Int J Oncol,2015,47(3): 1097-1102.
  • 9LI L Z, ZHANG C Z, LIU L L, et al. miR-720 inhibits tumor invasion and migration in breast cancer by targeting TWISTI[J]. Carcinogenesis,2014,35(2):469-478.
  • 10陈军,刘斌,孙毅,温敏.糖尿病并发皮肤溃疡的临床特点与治疗探讨[J].西部医学,2009,21(2):239-240. 被引量:3

引证文献25

二级引证文献75

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