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microRNA-128:肿瘤治疗新靶点 被引量:2

MicroRNA-128:A new target for oncotherapy
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摘要 微小RNA(miRNA)是体内一类长度为21~25个核苷酸的内源性非编码单链RNA,其主要通过完全或不完全互补结合至靶基因的3’非编码区而调控靶基因的表达。miRNA有多种类型,其中miR-128在多种疾病和正常组织中均不同程度的表达,具有广泛的调节作用。研究发现miR-128参与了神经胶质瘤、白血病、胃癌、肺癌及乳腺癌的发生过程,对细胞的分化、增殖、迁移和凋亡有重要作用。本文就miR-128在肿瘤中的研究进行详细阐述,以期为肿瘤的治疗提供新的靶点。 MicroRNA (miRNA) is a kind of small endogenous non-coding single RNA containing 21-25 nucleotides, which regulates the expression of target genes through complementary binding to the 3' untranslated region completely or incompletely. MiR-128, one of the subtypes of miRNA, expresses differently in a variety of diseases and normal tissues and plays an enormous role. Studies found that miR-128 played fundamental roles in various aspects of cellular function including differentiation, proliferation, migration and apoptosis in the development of several kinds of tumors including glioma, leukemia, stomach cancer, lung cancer and breast cancer. In this review, we will articulate the relationship between miR-128 and cancers, hoping to provide a new target for the treatment of tumor.
出处 《临床肿瘤学杂志》 CAS 2014年第9期849-853,共5页 Chinese Clinical Oncology
基金 国家自然科学基金资助项目(81270420) 湖南省高校创新平台开放基金资助项目(10K051) 湖南省自然科学基金省市联合(衡阳)基金重点项目(12JJ8013)
关键词 miR-128 胶质瘤 白血病 靶基因 调控机制 MicroRNA-128 Glioma Leukemia Target gene Regulatory mechanism
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参考文献33

  • 1Hell MP, Thoma CR, Fankhauser N, et al. miR-28-5p promotes chromosomal instability in VHL-associated cancers by inhibiting Mad2 translation[J]. Cancer Res, 2014, 74(9) :2432-2443.
  • 2Quintavalle C, Garofalo M, Zanca C, et al. miR-221/222 over- expession in human glioblastoma increases invasiveness by targeting the protein phosphate PTPmu [ J ]. Oncogene, 2012, 31 (7) :858-868.
  • 3Godlewski J, Nowicki MO, Bronisz A, et al. Targeting of the Bmi-1 oncogene/stem cell renewal factor by microRNA-128 inhibits glioma proliferation and self-renewal [ J ]. Cancer Res, 2008, 68(22) :9125-9130.
  • 4Wuchty S, Arjona D, Li A, et al. Prediction of associations be-tween microRNAs and gene expression in glioma biology [ J ]. PLoS One, 2011 [ 2014-03-15 ]. http://www, ncbi.nlm, nih. gov! pmc/articles/PMC3040173.
  • 5Zhang Y, Chao T, Li R, et al. MicroRNA-128 inhibits glioma ceils proliferation by targeting transcription factor E2F3a [ J ]. J Mol Med (Bed), 2009, 87(1):43-51.
  • 6Papagiannakopoulos T, Friedmann-Morvinski D, Neveu P, et al. Pro-neural miR-128 is a glioma tumor suppressor that targets mito- genic kinases[J]. Oncogene, 2012, 31(15):1884-1895.
  • 7Shi ZM, Wang J, Yan Z, et al. MiR-128 inhibits tumor growth and angiogenesis by targeting pTOS6K1 [ J ]. PLoS One, 2012 [ 2014-03-20 ]. http://www, ncbi. nlm. nih. gov/pmc/ articles/PMC3307714.
  • 8Nan WU Guo-cai WU Rong HU Mei LI Hua FENG.Ginsenoside Rh2 inhibits glioma cell proliferation by targeting microRNA-128[J].Acta Pharmacologica Sinica,2011,32(3):345-353. 被引量:34
  • 9Cui JG, Zhao Y, Sethi P, et al. Micro-RNA-128 (miRNA-128) down-regulation in glioblastoma targets ARP5 (ANGPTL6), Bmi-1 and E2F-3a, key regulators of brain cell proliferation[ J]. J Neurooncol, 2010, 98(3):297-304.
  • 10夏红飞,贺天柱,崔熠,马旭.miR-128真核表达载体的构建及功能的初步研究[J].生殖医学杂志,2010,19(2):146-151. 被引量:1

二级参考文献54

  • 1Kim VN.Small RNAs:classification,biogenesis,and function[J].Mol Cells,2005,19(1):1-15.
  • 2Hatfield SD,Shcherbata HR,Fischer KA,et al.Stem cell division is regulated by the microRNA pathway[J].Nature,2005,435(7044):974-978.
  • 3Karp X,Ambros V.Developmental biology.Encountering microRNAs in cell fate signaling[J].Science,2005,310(5752):1288-1289.
  • 4Lee RC,Feinbaum RL,Ambros V.The C.elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14[J].Cell,1993,75(5):843-854.
  • 5Griffiths-Jones S,Saini HK,van Dongen S,et al.miRBase:tools for microRNA genomics[J].Nucleic Acids Res,2008,36(Database issue):D154-D158.
  • 6Lim LP,Glasner ME,Yekta S,et al.Vertebrate microRNA genes[J].Science,2003,299(5612):1540.
  • 7Seggerson K,Tang L,Moss EG.Two genetic circuits repress the Caenorhabditis elegans heterochronic gene lin-28 after translation initiation[J].Dev Biol,2002,243(2):215-225.
  • 8Lin SY,Johnson SM,Abraham M,et al.The C.elegans hunchback Homolog,hbl-1,controls temporal patterning and is a probable microRNA target[J].Dev Cell,2003,4(5):639-650.
  • 9Houbavity HB,Murry MF,Sharp PA.Embryo stem stem cell-specific MicroRNAs[J].Dev Cell,2003,5(2):351-358.
  • 10Lagos-Quintana M,Rauhut R,Meyer J,et al.New microRNAs from mouse and human[J].RNA,2003,9(2):175-179.

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