4.6 Review

Nanoparticle-mediated delivery of therapeutic genes: focus on miRNA therapeutics

Journal

EXPERT OPINION ON DRUG DELIVERY
Volume 10, Issue 9, Pages 1259-1273

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1517/17425247.2013.798640

Keywords

microRNA; nanocarriers; oncogene; therapeutics; tumor suppressor gene

Funding

  1. BioImaging Research Center at GIST
  2. Regional Technology Innovation Program of the Ministry of Commerce, Industry and Energy [RT104-01-01]
  3. Basic Science Research Program through the National Research Foundation of Korea (NRF)
  4. Ministry of Education, Science and Technology (MEST) [2010-0002940]
  5. Korea Healthcare Technology R&D Project, Ministry for Health, Welfare & Family Affairs, Republic of Korea [A120899]
  6. Small and Medium Business Administration of Korea
  7. Leading Foreign Research Institute Recruitment Program through the NRF
  8. MEST [2011-0030034, 2012-0001034]
  9. Future Pioneer R&D program through the NRF
  10. Ministry of Science & ICT (MSIT), Republic of Korea [GIST-12] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  11. National Research Foundation of Korea [2009-0082952, 2011-0030034] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Introduction: Micro RNAs (miRNA) are 21 - 23 nucleotides long and regulate the expression of coding genes by binding imperfectly with their 3' UTR region. The miRNA profile is altered in pathological processes, making miRNAs good targets for drug therapy. Restoration of down-regulated miRNA or inhibition of overexpressed miRNA to return miRNA to its normal state is the basis of miRNA-based therapy. This review focuses on nanocarriers used for the delivery of miRNA that confer physical stability to the unstable RNA structure, protect the RNA from nuclease degradation and aid in effective silencing of target genes. Areas covered: The necessity of the nanocarrier for the delivery of the miRNA is emphasized and the recent research on liposome-, metal- and polymer-mediated miRNA delivery for the inhibition or replacement of the disease-related miRNA is summarized. Expert opinion: The size, charge and surface properties of nanocarriers have to be tuned to ensure effective and safe delivery of the miRNA in clinical practice. The immune responses related to the nanocarriers and the double-stranded nucleotide delivery remain to be addressed. Also, the binding of miRNAs to non-specific targets has to be studied in more detail because miRNAs have multiple targets due to partial binding unlike siRNA.

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