Prenyl Ammonium Salts--New Carriers for Gene Delivery: A B16-F10 Mouse Melanoma Model

PLoS One. 2016 Apr 18;11(4):e0153633. doi: 10.1371/journal.pone.0153633. eCollection 2016.

Abstract

Purpose: Prenyl ammonium iodides (Amino-Prenols, APs), semi-synthetic polyprenol derivatives were studied as prospective novel gene transfer agents.

Methods: AP-7, -8, -11 and -15 (aminoprenols composed of 7, 8, 11 or 15 isoprene units, respectively) were examined for their capacity to form complexes with pDNA, for cytotoxicity and ability to transfect genes to cells.

Results: All the carriers were able to complex DNA. The highest, comparable to commercial reagents, transfection efficiency was observed for AP-15. Simultaneously, AP-15 exhibited the lowest negative impact on cell viability and proliferation--considerably lower than that of commercial agents. AP-15/DOPE complexes were also efficient to introduce pDNA to cells, without much effect on cell viability. Transfection with AP-15/DOPE complexes influenced the expression of a very few among 44 tested genes involved in cellular lipid metabolism. Furthermore, complexes containing AP-15 and therapeutic plasmid, encoding the TIMP metallopeptidase inhibitor 2 (TIMP2), introduced the TIMP2 gene with high efficiency to B16-F10 melanoma cells but not to B16-F10 melanoma tumors in C57BL/6 mice, as confirmed by TIMP2 protein level determination.

Conclusion: Obtained results indicate that APs have a potential as non-viral vectors for cell transfection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ammonium Compounds / pharmacology*
  • Animals
  • Blotting, Western
  • Cell Survival
  • DNA / administration & dosage*
  • Drug Carriers
  • Drug Delivery Systems*
  • Female
  • Gene Transfer Techniques
  • Genetic Therapy*
  • Immunoenzyme Techniques
  • Liposomes
  • Lung Neoplasms / genetics
  • Lung Neoplasms / secondary
  • Lung Neoplasms / therapy
  • Melanoma, Experimental / genetics
  • Melanoma, Experimental / pathology
  • Melanoma, Experimental / therapy*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Neoprene / chemistry*
  • RNA, Messenger / genetics
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sarcoma, Experimental / genetics
  • Sarcoma, Experimental / pathology
  • Sarcoma, Experimental / therapy*
  • Transfection
  • Tumor Cells, Cultured
  • Xenograft Model Antitumor Assays

Substances

  • Ammonium Compounds
  • Drug Carriers
  • Liposomes
  • RNA, Messenger
  • prenyl
  • DNA
  • Neoprene

Grants and funding

This work was supported by Polish National Cohesion Strategy Innovative Economy Grant UDA-POIG 01.03.01-14-036/09 (ES, MC, M. Malecki). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.