Emerging Role of microRNA in Neuropathic Pain

被引:51
作者
Pu Jiangpan [1 ,4 ]
Meng Qingsheng [2 ,3 ]
Yang Zhiwen [1 ]
Zhu Tao [1 ]
机构
[1] Nanjing Med Univ, Shanghai Songjiang Hosp, Shanghai, Peoples R China
[2] Nanjing Med Univ, Nanjing Hosp, Dept Anesthesiol, Nanjing 210006, Jiangsu, Peoples R China
[3] Nanjing First Hosp, Nanjing 210006, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Nanjing, Jiangsu, Peoples R China
关键词
Delivery; mechanism; microRNA; neuropathic pain; side-effect; targeting; DIFFERENTIAL EXPRESSION; ANTISENSE OLIGONUCLEOTIDES; RNAI THERAPEUTICS; NERVOUS-SYSTEM; SPINAL-CORD; RAT MODEL; IN-VIVO; DELIVERY; CANCER; MIRNA;
D O I
10.2174/1389200216666151015113400
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
Background: Neuropathic pain is an incurable disease which is defined as a chronic pain caused by a disease or lesion of the nervous systems. Current treatments can provide a long-lasting pain relief only in a very limited number of patients with neuropathic pain. MicroRNA can regulate multiple genes and pathways involved in human diseases. This review focuses on: a) Molecular mechanisms of microRNA biogenesis. b) Targeting, modifications, and delivery of microRNAs. c) Aberrant expression of microRNAs and their potential therapeutic targets in neuropathic pain. d) Potential challenges of microRNA therapy in clinical practice, such as off-target effects, toxicity, delivery hurdles, and target prediction. Results: This review introduces: 1. Canonical/non-canonical pathway of microRNA biogenesis. 2. Viral/non-viral vectors transporting microRNAs into target cells. 3. MicroRNA mimics/inhibitors targeting strategies. 4. Aberrantly expressed microRNAs in different animal neuropathic pain models and their links to underlying mechanisms such as inflammation and ion channel expression. 5. Potential challenges of microRNAs therapy such as off-target effect, pseudogenes, liver toxicity, delivery hurdles and target prediction. Conclusion: Although using microRNAs to target neuropathic pain seem promising, their off-target/toxic effects and delivery hurdles still need to be surmounted.
引用
收藏
页码:336 / 344
页数:9
相关论文
共 79 条
  • [1] CHANGES IN EXPRESSION OF SENSORY ORGAN-SPECIFIC microRNAs IN RAT DORSAL ROOT GANGLIA IN ASSOCIATION WITH MECHANICAL HYPERSENSITIVITY INDUCED BY SPINAL NERVE LIGATION
    Aldrich, B. T.
    Frakes, E. P.
    Kasuya, J.
    Hammond, D. L.
    Kitamoto, T.
    [J]. NEUROSCIENCE, 2009, 164 (02) : 711 - 723
  • [2] MicroRNAs as modulators and biomarkers of inflammatory and neuropathic pain conditions
    Andersen, Hjalte H.
    Duroux, Meg
    Gazerani, Parisa
    [J]. NEUROBIOLOGY OF DISEASE, 2014, 71 : 159 - 168
  • [3] Efficient delivery of RNA Interference to peripheral neurons in vivo using herpes simplex virus
    Anesti, Anna-Maria
    Peeters, Pieter J.
    Royaux, Ines
    Coffin, Robert S.
    [J]. NUCLEIC ACIDS RESEARCH, 2008, 36 (14)
  • [4] The miRNA and mRNA Changes in Rat Hippocampi after Chronic Constriction Injury
    Arai, Masae
    Genda, Yuuki
    Ishikawa, Masashi
    Shunsuke, Tanaka
    Okabe, Tadashi
    Sakamoto, Atsuhiro
    [J]. PAIN MEDICINE, 2013, 14 (05) : 720 - 729
  • [5] The Promise of MicroRNA Replacement Therapy
    Bader, Andreas G.
    Brown, David
    Winkler, Matthew
    [J]. CANCER RESEARCH, 2010, 70 (18) : 7027 - 7030
  • [6] Noncoding RNAs: key molecules in understanding and treating pain
    Bali, Kiran Kumar
    Kuner, Rohini
    [J]. TRENDS IN MOLECULAR MEDICINE, 2014, 20 (08) : 437 - 448
  • [7] Global Coevolution of Human MicroRNAs and Their Target Genes
    Barbash, Shahar
    Shifman, Sagiv
    Soreq, Hermona
    [J]. MOLECULAR BIOLOGY AND EVOLUTION, 2014, 31 (05) : 1237 - 1247
  • [8] Expression of spinal cord microRNAs in a rat model of chronic neuropathic pain
    Brandenburger, Timo
    Castoldi, Mirco
    Brendel, Maike
    Grievink, Hilbert
    Schloesser, Lukas
    Werdehausen, Robert
    Bauer, Inge
    Hermanns, Henning
    [J]. NEUROSCIENCE LETTERS, 2012, 506 (02) : 281 - 286
  • [9] MicroRNA silencing improves the tumor specificity of adenoviral transgene expression
    Card, P. B.
    Hogg, R. T.
    del Alcazar, C. R. Gil
    Gerard, R. D.
    [J]. CANCER GENE THERAPY, 2012, 19 (07) : 451 - 459
  • [10] The promises and pitfalls of RNA-interference-based therapeutics
    Castanotto, Daniela
    Rossi, John J.
    [J]. NATURE, 2009, 457 (7228) : 426 - 433