MicroRNA polymorphisms: the future of pharmacogenomics, molecular epidemiology and individualized medicine

被引:222
作者
Mishra, Prasun J. [1 ]
Bertino, Joseph R. [2 ]
机构
[1] NCI, Lab Canc Biol & Genet, NIH, Bethesda, MD 20892 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Newark, NJ 07103 USA
关键词
classification; diagnosis; disease; drug resistance; epidemiology; epigenetics; microRNA; miRSNP; mutations; pharmacogenomics; polymorphism; prognosis; SNP; SINGLE-NUCLEOTIDE POLYMORPHISM; DIHYDROFOLATE-REDUCTASE GENE; BINDING-SITE POLYMORPHISM; MESSENGER-RNA; BREAST-CANCER; TARGET SITE; UNTRANSLATED REGION; EXPRESSION; RISK; CELL;
D O I
10.2217/14622416.10.3.399
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Referred to as the micromanagers of gene expression, microRNAs (miRNAs) are evolutionarily conserved small noncoding RNAs. Polymorphisms in the miRNA pathway (miR-polymorphisms) are emerging as powerful tools to study the biology of a disease and have the potential to be used in disease prognosis and diagnosis. Detection of miR-polymorphisms holds promise in the field of miRNA pharmacogenomics, molecular epidemiology and for individualized medicine. MiRNA pharmacogenomics can be defined as the study of miRNAs and polymorphisms affecting miRNA function in order to predict drug behavior and to improve drug efficacy. Advancements in the miRNA field indicate the clear involvement of miRNAs and genetic variations within the miRNA pathway in the progression and prognosis of diseases such as cancer, neurological disorders, muscular hypertrophy, gastric mucosal atrophy, cardiovascular disease and Type 11 diabetes. Various algorithms are available to predict miRNA-target mRNA sites; however, it is advisable to use multiple algorithms to confirm the predictions. Polymorphisms that may potentially affect miRNA-mediated regulation of the cell can be present not only in the 3'-UTR of a miRNA target gene, but also in the genes involved in miRNA biogenesis and in pri-, pre- and mature-miRNA sequences. A polymorphism in processed miRNAs may affect expression of several genes and have serious consequences, whereas a polymorphism in miRNA target site, in the 3'-UTR of the target mRNA, may be more target and/or pathway specific. In this review, we for the first time suggest a classification of miRNA polymorphisms/mutations. We also describe the importance and implications of miR-polymorphisms in gene regulation, disease progression, pharmacogenomics and molecular epidemiology.
引用
收藏
页码:399 / 416
页数:18
相关论文
共 96 条
  • [41] MicroRNA gene expression deregulation in human breast cancer
    Iorio, MV
    Ferracin, M
    Liu, CG
    Veronese, A
    Spizzo, R
    Sabbioni, S
    Magri, E
    Pedriali, M
    Fabbri, M
    Campiglio, M
    Ménard, S
    Palazzo, JP
    Rosenberg, A
    Musiani, P
    Volinia, S
    Nenci, I
    Calin, GA
    Querzoli, P
    Negrini, M
    Croce, CM
    [J]. CANCER RESEARCH, 2005, 65 (16) : 7065 - 7070
  • [42] Common SNP in pre-miR-146a decreases mature miR expression and predisposes to papillary thyroid carcinoma
    Jazdzewski, Krystian
    Murray, Elizabeth L.
    Franssila, Kaarle
    Jarzab, Barbara
    Schoenberg, Daniel R.
    de la Chapelle, Albert
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (20) : 7269 - 7274
  • [43] JENSEN KP, MOL PSYCHIATR, DOI DOI 10.1038/MP.2008.15
  • [44] Involvement of MicroRNA in AU-rich element-mediated mRNA instability
    Jing, Q
    Huang, S
    Guth, S
    Zarubin, T
    Motoyama, A
    Chen, JM
    Di Padova, F
    Lin, SC
    Gram, H
    Han, JH
    [J]. CELL, 2005, 120 (05) : 623 - 634
  • [45] Human microRNA targets (vol 2, pg 1862, 2005)
    John, B
    Enright, AJ
    Aravin, A
    Tuschl, T
    Sander, C
    Marks, DS
    [J]. PLOS BIOLOGY, 2005, 3 (07): : 1328 - 1328
  • [46] First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome
    Kapeller, Johannes
    Houghton, Lesley A.
    Moennikes, Hubert
    Walstab, Jutta
    Moeller, Dorothee
    Boenisch, Heinz
    Burwinkel, Barbara
    Autschbach, Frank
    Funke, Benjamin
    Lasitschka, Felix
    Gassler, Nikolaus
    Fischer, Christine
    Whorwell, Peter J.
    Atkinson, Wendy
    Fell, Catherine
    Buechner, Karl J.
    Schmidtmann, Marco
    van der Voort, Ivo
    Wisser, Anna-Sophia
    Berg, Thomas
    Rappold, Gudrun
    Niesler, Beate
    [J]. HUMAN MOLECULAR GENETICS, 2008, 17 (19) : 2967 - 2977
  • [47] A small piece in the cancer puzzle: microRNAs as tumor suppressors and oncogenes
    Kent, O. A.
    Mendell, J. T.
    [J]. ONCOGENE, 2006, 25 (46) : 6188 - 6196
  • [48] The role of site accessibility in microRNA target recognition
    Kertesz, Michael
    Iovino, Nicola
    Unnerstall, Ulrich
    Gaul, Ulrike
    Segal, Eran
    [J]. NATURE GENETICS, 2007, 39 (10) : 1278 - 1284
  • [49] Combinatorial microRNA target predictions
    Krek, A
    Grun, D
    Poy, MN
    Wolf, R
    Rosenberg, L
    Epstein, EJ
    MacMenamin, P
    da Piedade, I
    Gunsalus, KC
    Stoffel, M
    Rajewsky, N
    [J]. NATURE GENETICS, 2005, 37 (05) : 495 - 500
  • [50] Experimental validation of miRNA targets
    Kuhn, Donald E.
    Martin, Mickey M.
    Feldman, David S.
    Terry, Alvin V., Jr.
    Nuovo, Gerard J.
    Elton, Terry S.
    [J]. METHODS, 2008, 44 (01) : 47 - 54