Is miR therapeutic targeting still a miRage?

被引:7
作者
Levantini, Elena [1 ,2 ,3 ,4 ]
机构
[1] Harvard Med Sch, Boston, MA 02115 USA
[2] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[3] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[4] Natl Res Council CNR, Inst Biomed Technol, Area Ric Pisa, I-56124 Pisa, Italy
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2021年 / 26卷 / 10期
关键词
RNA therapeutics; Biomarkers; miR-21; NSCLC; Cancer; CELL LUNG-CANCER; HUMAN MICRORNA GENES; TUMOR-SUPPRESSOR; DOWN-REGULATION; GASTRIC-CANCER; LINKING INFLAMMATION; CURRENT STRATEGIES; NONCODING RNAS; MESSENGER-RNAS; EXPRESSION;
D O I
10.52586/4979
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Since the discovery of the first microRNA (miR), almost three decades ago, the roles played by miRs under normal and diseased settings have been widely investigated. miRs are found to play crucial roles in cancer initiation and progression, as well as towards therapy response mechanisms. Therefore, they are relevant and attractive targets for therapeutic development. Many preclinical studies have demonstrated their promise as future anti-cancer tools. Recently, increasing number of early phase clinical trials have emerged. In this Commentary, we will summarize the major discoveries within the miR research field and highlight the status quo of current miR-therapeutics, which has prominent potential of impacting future cancer regimens given their massive dysregulation in oncogenic processes.
引用
收藏
页码:680 / 692
页数:13
相关论文
共 201 条
  • [1] A uniform system for microRNA annotation
    Ambros, V
    Bartel, B
    Bartel, DP
    Burge, CB
    Carrington, JC
    Chen, XM
    Dreyfuss, G
    Eddy, SR
    Griffiths-Jones, S
    Marshall, M
    Matzke, M
    Ruvkun, G
    Tuschl, T
    [J]. RNA, 2003, 9 (03) : 277 - 279
  • [2] microRNAs: Tiny regulators with great potential
    Ambros, V
    [J]. CELL, 2001, 107 (07) : 823 - 826
  • [3] Diversifying microRNA sequence and function
    Ameres, Stefan L.
    Zamore, Phillip D.
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2013, 14 (08) : 475 - 488
  • [4] Epstein-Barr virus encoded LMP1 downregulates TCL1 oncogene through miR-29b
    Anastasiadou, E.
    Boccellato, F.
    Vincenti, S.
    Rosato, P.
    Bozzoni, I.
    Frati, L.
    Faggioni, A.
    Presutti, C.
    Trivedi, P.
    [J]. ONCOGENE, 2010, 29 (09) : 1316 - 1328
  • [5] MicroRNA-21 (miR-21) post-transcriptionally downregulates tumor suppressor Pdcd4 and stimulates invasion, intravasation and metastasis in colorectal cancer
    Asangani, I. A.
    Rasheed, S. A. K.
    Nikolova, D. A.
    Leupold, J. H.
    Colburn, N. H.
    Post, S.
    Allgayer, H.
    [J]. ONCOGENE, 2008, 27 (15) : 2128 - 2136
  • [6] audelot K, 2017, TUMOR BIOL, V39
  • [7] Hypoxia represses microRNA biogenesis proteins in breast cancer cells
    Bandara, Veronika
    Michael, Michael Z.
    Gleadle, Jonathan M.
    [J]. BMC CANCER, 2014, 14
  • [8] Metazoan MicroRNAs
    Bartel, David P.
    [J]. CELL, 2018, 173 (01) : 20 - 51
  • [9] MicroRNAs: Target Recognition and Regulatory Functions
    Bartel, David P.
    [J]. CELL, 2009, 136 (02) : 215 - 233
  • [10] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29