Gene Therapy Techniques;Physical and Chemical Methods
Veysi Akpolat (Author)
Release Date: 2024-02-12
Gene therapy is a technique that changes a person’s genes to treat or cure disease. To insert new genes directly into cells, scientists use a tool called a “vector.” Vectors are genetically engineered to deliver the genes needed to treat the disease. Various approaches can be used to deliver DNA into the cell with different [...]
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Work Type | Book Chapter |
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Published in | Gene Therapy |
First Page | 17 |
Last Page | 38 |
DOI | https://doi.org/10.69860/nobel.9786053358824.2 |
Page Count | 22 |
Copyright Holder | Nobel Tıp Kitabevleri |
License | https://nobelpub.com/publish-with-us/copyright-and-licensing |
Veysi Akpolat (Author)
Professor, Dicle University
https://orcid.org/0000-0002-2435-7800
3Veysi Akpolat, currently works as a professor at Dicle University, Department of Biophysics. He graduated from Dicle University Faculty of Medicine with the title of Medical Doctor in 1990. Later, he completed his doctorate in the biophysics department of Dicle University Faculty of Medicine in 2004. He has many research and projects on cell biophysics. He has many research and projects on cell biophysics. The areas he is most interested in are ion channels diseases, electromagnetic field cell interactions, electrophysiological biopotentials, osteoporosis, artificial intelligence and its use in medicine.
https://www.fda.gov/consumers/consumer-updates/how-gene-therapy-can-cure-ortreat- diseases?%20how%20does%20it%20work?.
Attar A. Gene therapy techniques: physical and chemical methods. Turk Hij Den Biyol Derg, 2017; 74(1): 103-112.
Long Term Follow-Up After Administration of Human Gene Therapy Products; Guidance for Industry, January 2020. Followed by ; https://www.fda.gov/vaccines- blood-biologics/cellular-gene-therapy-products/what-gene-therapy.
https://www.nhlbi.nih.gov/health/genetic-therapies/types.
W.T. Godbey, Chapter 13- gene delivery, in: W.T. Godbey (Ed.), An Introduction to Biotechnology, Woodhead Publishing, 2014, pp. 275–312.
Y.T. Chow, et al., Single cell transfection through precise microinjection with quantitatively controlled injection volumes, Sci. Rep. 6 (1) (2016) 24127.
J.A. O’Brien, S.C.R. Lummis, Nano-biolistics: a method of biolistic transfection of cells and tissues using a gene gun with novel nanometer-sized projectiles, BMC Biotechnol. 11 (1) (2011) 66.
C.H. Yang, et al., Seeing the gene therapy: application of gene gun technique to transfect and decolour pigmented rat skin with human agouti signalling protein cDN, Gene Ther. 11 (13) (2004) 1033–1039.
W. F¨orster, E. Neumann, Gene transfer by electroporation, in: E. Neumann, A. E. Sowers, C.A. Jordan (Eds.), Electroporation and Electrofusion in Cell Biology, Springer US, Boston, MA, 1989, pp. 299–318.
L.D. Cervia, F. Yuan, Current Progress in electrotransfection as a nonviral method for gene delivery, Mol. Pharm. 15 (9) (2018) 3617–3624.
J.L. Young, D.A. Dean, Electroporation-mediated gene delivery, Adv. Genet. 89 (2015) 49–88.
Bulysheva A., et al., 365. Increased tissue temperature improves electro-transfer mediated gene delivery to skin, Mol. Ther. 23 (2015), S145.
Tao W., Wilkinson J., Stanbridge EJ., Berns MW. Direct gene transfer into human cultured cells facilitated by laser micropuncture of the cell membrane. Proc Natl Acad Sci USA, 1987; 84 (12): 4180-4.
Palumbo G., Caruso M., Crescenzi E., Tecce MF., Roberti G., Colasanti A. Targeted gene transfer in eucaryotic cells by dye-assisted laser optoporation. J Photochem Photobiol B: Biol, 1996; 36 (1): 41-6.
Sagi S, Knoll T, Trojan L, Schaaf A, Alken P, Michel MS. Gene delivery into prostate cancer cells by holmium laser application. Prostate Cancer Prostatic Dis, 2003; 6 (2): 127-30.
Zeira E., et al. Femtosecond infrared laser-an efficient and safe in vivo gene delivery system for prolonged expression. Molec Ther, 2003; 8 (2): 342-50.
Clark I., et al., Optoinjection for efficient targeted delivery of a broad range of compounds and macromolecules into diverse cell types, J. Biomed. Opt. 11 (1) (2006), 014034. 17780–17789.
Sakakura, M., et al., Observation of laser-induced stress waves and mechanism of structural changes inside rock-salt crystals, Opt. Express 19 (18) (2011).
Yao CP., et al., Laser-based gene transfection and gene therapy, IEEE Trans. Nanobioscience 7 (2) 111–119. (2008).
Farivar S., Malekshahabi T., Shiari R. Biological effects of low level laser therapy, J Lasers Med Sci 5 (2) 58–62. (2014).
W. Jerjes., et al., Photochemical internalization for intracellular drug delivery. From basic mechanisms to clinical research, J. Clin. Med. 9 (2), 528. (2020).
Pitsillides CM., et al., Selective cell targeting with light-absorbing microparticles and nanoparticles, Biophys. J. 84 (6) 4023–4032. (2003).
Passineau MJ., et al., Ultrasound-assisted non-viral gene transfer to the salivary glands, Gene Ther. 17 (11) (2010) 1318–1324.
Tomizawa M., et al., Sonoporation: gene transfer using ultrasound, World J. Methodol. 3 (4) (2013) 39.
Scherer F, Anton M, Schillinger U, Henke J, Bergemann C, Kruger A, et al. Magnetofection: Enhancing and targeting gene delivery by magnetic force in vitro and in vivo. Gene Ther, 2002; 9 (2): 102-9.
Yellepeddi V., in: Vectors for Non-viral Gene Delivery-Clinical and Biomedical Applications, Austin Therapeutics,, pp. 2472–3673. (2015).
Krötz F., Sohn HY., Gloe T., Plank C., Pohl U. Magnetofection potentiates gene delivery to cultured endothelial cells. J Vasc Res, 2003; 40 (5): 425-34.
Suda T., Liu D. Hydrodynamic gene delivery: its principles and applications, Mol. Ther. 15 (12) 2063–2069. (2007).
Kedika B., Patri SV. Benzothiazole head group based cationic lipids: synthesis and application for gene delivery. Eur J Med Chem, 2014; 74: 703-716.
Balazs DA., Godbey W. Liposomes for use in gene delivery, J. Drug Deliv. 2011, 326497. (2011).
Hug P., Sleight RG. Chapter 18 The advantages of liposome-based gene therapy: a comparison of viral versus liposome-based gene delivery, in: Bittar E.E., Bittar N. (Eds.), Principles of Medical Biology, Elsevier, 1997, pp. 345–362.
Balbino TA, Azzoni AR, de La Torre LG. Microfluidic devices for continuous production of pDNA/cationic liposome complexes for gene delivery and vaccine therapy. Colloids Surf B Biointerfaces, 2013; 111: 203-210.
Renukuntla J, Vadlapudi AD, Patel A, Boddu SH, Mitra AK. Approaches for enhancing oral bioavailability of peptides and proteins. Int J Pharm, 2013; 447: 75-93.
Hebert E. Improvement of exogenous DNA nuclear importation by nuclear localization signal-bearing vectors: a promising way for nonviral gene therapy. Biol Cell, 2003; 95 (2): 59-68.
Lakkaraju A, Dubinsky JM, Low WC, Rahman Y-E. Neurons are protected from excitotoxic death by p53 antisense oligonucleotides delivered in anionic liposomes. J Biol Chem, 2001; 276: 32000-7.
Fillion P, Desjardins A, Sayasith K, Lagace J. Encapsulation of DNA in negatively charged liposomes and inhibition of bacterial gene expression with fluid liposome-encapsulated antisense oligonucleotides. Biochim Biophys Acta, 2001; 1515: 44-54.
Perrie Y., Gregoriadis G. Liposome-entrapped plasmid DNA: Characterization studies. Biochim Biophys Acta, 2000; 1475: 125-32.
Patil SD, Rhodes DG, Burgess DJ. Anionic liposomal delivery system for DNA transfection. The AAPS Journal, 2004; 6 (4): 1-10.
Attar A, Ogan A, Yucel S, Turan K. The potential of archaeosomes as carriers of pDNA into mammalian cells. Artif Cells Nanomed Biotechnol, 2016; 44: 710-6.
Sayed N., et. al., Gene therapy: Comprehensive overview and therapeutic applications. Life Sci. 2022 Apr 1; 294:120375.
Calcium phosphate–mediated transfection of eukaryotic cells, Nat. Methods 2 (4) (2005) 319–320.
K.D. Mack, et al., A novel method for DEAE-dextran mediated transfection of adherent primary cultured human macrophages, J. Immunol. Methods 211 (1–2) (1998) 79–86.
Mortimer I., et al., Cationic lipid-mediated transfection of cells in culture requires mitotic activity, Gene Ther. 6 (3) 403–411. (1999).
Felgner J., et al., Cationic lipid-mediated transfection in mammalian cells: “Lipofection”, J. Tissue Cult. Methods 15 (2) 63–68. (1993).
Zhu L., Mahato RI., Lipid and polymeric carrier-mediated nucleic acid delivery, Expert Opin. Drug Deliv. 7 (10) 1209–1226. (2010).
Barua S., et al., Discovery of cationic polymers for non-viral gene delivery using combinatorial approaches, Comb. Chem. High Throughput Screen. 14 (10) 908–924. (2011).
Eliyahu H., Barenholz Y., Domb AJ. Polymers for DNA delivery, Molecules 10 (1) 34–64. (2005).
Ramamoorth M., Narvekar A. Non-viral vectors in gene therapy- an overview, J. Clin. Diagn. Res. 9 (1) GE01-6. (2015).
Bates K., Kostarelos K. Carbon nanotubes as vectors for gene therapy: past achievements, present challenges and future goals, Adv. Drug Deliv. Rev. 65 (15) (2013).
Maeda-Mamiya, R., et al., In vivo gene delivery by cationic tetra amino fullerene, Proc. Natl. Acad. Sci. U. S. A. 107 (12) 5339–5344. (2010).
Shalek AK., et al., Vertical silicon nanowires as a universal platform for delivering biomolecules into living cells, Proc. Natl. Acad. Sci. U. S. A. 107 (5) 1870–1875. (2010).
Cao X., et al., Photoluminescent cationic carbon dots as efficient non-viral delivery of plasmid SOX9 and chondrogenesis of fibroblasts, Sci. Rep. 8 (1) 7057. (2018).
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