Gene therapy is broadly defined as the delivery or transferof genetic material to target cells for therapeutic purposes. Elucidation of the molecular bases of inherited diseases as well as acquired diseases, such as cancer, allows for the possibility of therapeutic interventions at the molecular level. The therapeutic benefits may be achieved by, interfering with gene function, restoring lost function, or initiating a new function in the target cells. Current methods of gene transfer include the use of viral and non-viral vectors [1–5]. Viral vectors accomplish gene transfer directly by viral-mediated infection.
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- AAV:
-
adeno-associated viruses
- Ad5:
-
type of adenovirus
- Ad-ER-DN:
-
adenoviral vector that expresses a dominant negative ER mutant
- Ad-LacZ:
-
adenovirus expressing the marker gene β-lactamase
- ALDH-1:
-
aldehyde dehydrogenase class 1 gene
- bFGF:
-
basic fibroblast growth factor
- CaCL2:
-
calcium chloride
- CAR:
-
coxsackie-adenovirus receptor
- CD/5-FCyt:
-
cytosine deaminase plus 5-fluorocytosine
- CMV:
-
cytomegalovirus
- CRAds:
-
conditionally replicative adenoviruses
- DNA:
-
deoxyribonucleic acid
- ELT3:
-
cell line derived from Eker rat leiomyoma
- ER:
-
estrogen receptor
- ERE:
-
estrogen receptor element
- ERI-536:
-
estrogen receptor mutant
- GCV:
-
ganciclovir
- HSV:
-
herpes simplex virus
- HSV-tk:
-
herpes simplex virus-thymidine kinase
- LM-15:
-
human leiomyoma cell line
- MDR1:
-
multidrug resistance gene
- MOI:
-
multiplicity of infection
- PDGF:
-
platelet-derived endothelial growth factor
- RNA:
-
ribonucleic acid
- siRNA:
-
small interfering RNA
- TK-GCV:
-
thymidine kinase – ganciclovir
- TNF:
-
tumor necroses factor
- TRAIL:
-
TNF apoptosis-inducing ligand
- VEGF:
-
vascular endothelial growth factor
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Al-Hendy, A., Salama, S.A. (2009). Introduction to Gene Therapy. In: Chedrese, P. (eds) Reproductive Endocrinology. Springer, Boston, MA. https://doi.org/10.1007/978-0-387-88186-7_12
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