Development of drug targeting based on recombinant expression of the chicken avidin gene

Journal of Drug Targeting

Volumn 4, Issue 1, 1996, Pages 41-49

  Walker, Lynn ^a   Kulomaa, Markku S ^d   Bebok, Zsuzsa ^b   Parker, William B ^c   Allan, Paula ^c   Logan, James ^a   Huang, Zhen ^b   Reynolds, Robert C ^c   King, Scott ^b   Sorscher, Eric J ^b  

^a University of Alabama at Birmingham   (United States)

^b UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^c SOUTHERN RESEARCH INSTITUTE   (United States)

^d UNIVERSITY OF JYVÄSKYLÄ   (Finland)

Author keywords

Avidin; Biotinylation; Drug targeting; Gene expression

Indexed keywords

ANTINEOPLASTIC AGENT; AVIDIN; BIOTIN; COMPLEMENTARY DNA; RADIOPHARMACEUTICAL AGENT; RECOMBINANT DNA; STREPTAVIDIN;

ANIMAL CELL; ARTICLE; BREAST CANCER; CONTROLLED STUDY; COVALENT BOND; DRUG SYNTHESIS; DRUG TARGETING; GENE EXPRESSION; GENE TARGETING; HELA CELL; HUMAN; HUMAN CELL; IMMUNOHISTOCHEMISTRY; NONHUMAN; OLIGOMERIZATION; PRIORITY JOURNAL; PROTEIN FOLDING; TUMOR CELL LINE;

EID: 9344259103     PISSN: 1061186X     EISSN: None     Source Type: Journal    
DOI: 10.3109/10611869609046259     Document Type: Article

References (34)

1. Alton, E.W.F.W., Middleton, P.G., et al. (1993). Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice. Nature/Genetics 5:16-23.
2. Bradford, M.M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72:248-254.
3. Canonico, A.B., Conary, J.T., et al. (1994). Aerosol and intravenous transfection of human α1-antitrypsin gene to lungs of rabbits. Am. J. Respir. Cell. Mol. Biol. 10:24-29.
4. Caplen, N.J., Alton, E.W.F.W., et al. (1995). Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis. Nat. Med. 1:38-46.
5. Caruso, M., Panis, Y., et al., (1993). Regression of established macroscopic liver metastases after in situ transduction of a suicide gene. Proc. Nat. Acad. Sci. USA, 90(15):7024-7028.
6. Chambers, R., Gillespie, G.Y., et al., (1995). Comparison of genetically engineered herpes simplex viruses for the treatment of brain tumors in a scid mouse model of human malignant glioma. Proc. Nat. Acad. Sci. USA, 92(5):1411-1415.
7. Chen, S.H., Shine, H.D., et al., (1994). Gene therapy for brain tumors: regression of experimental gliomas by adenovirus-mediated gene transfer in vivo. Proc. Nat. Acad. Sci. USA, 91(8):3054-7.
8. Culver, K.W., Ram, Z., et al. (1992). In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. Science, 256:1550-1552.
9. Freeman, S.M. Gene transfer for the treatment of cancer. RAC Protocol No. 9202-016, approved 2/10/92; NIH approval 2/4/ 93.
10. Gao, L., Wagner, E., et al., (1993). Direct in vivo gene transfer into airway epithelium employing adenovirus-polylysine-DNA complexes. Hum. Gen. Ther. 4(1):17-24.
11. Gope, M.L., Keinänen, R.A., et al. (1987). Molecular cloning of the chicken avidin cDNA. Nuc. Acids Res. 15:3595-3599.
12. Hnatowich, D.J., Virzi, F., et al. (1987). Investigations of avidin and biotin for imaging applications. J. Nucl. Med., 28:1294-1302.
13. Huber, B.E., Richards, C.A., and Krenitsky, T.A. (1991). Retroviral-mediated gene therapy for the treatment of hepatocellular carcinoma: an innovative approach for cancer therapy. Proc. Natl Acad. Sci. USA, 88:8039-8043.
14. Hughes, B., Parker W.B., Gadi V.K., Garver R.I, and Sorscher E.J. Bystander Killing of Melanoma Cells Using the Human Tyrosinase Promoter to Express the E. coli Purine Nucleoside Phosphorylase Gene. Cancer Research, 55:3339-3345 (1995).
15. 111indium labeled biotin and streptavidin-conjugated antibodies: preliminary communication. J. Nucl. Med., 31:1791-1796.
16. Kuriyama, S., Yoshikawa, M., et al. (1991). A potential approach for gene therapy targeting hepatoma using a liver-specific promoter on a retroviral vector. Cell Struct. Funct. 16:503-510.
17. Logon, J., Bebok, Z., Walker, L., Feigner, P., Burgess, S., Shaw, W., Siegal, G., Frizzell, R., Dong, J., Matalon, S., Duvall, M., Sorscher, E.J. (1995). Cationic lipids for CFTR gene transfer. Gene Therapy 2:38-49.
18. Manome, Y., Abe, M., et al. (1994). Enhancer sequences of the DF3 gene regulate expression of the herpes simplex virus thymidine kinase gene and confer sensitivity of human breast cancer cells to ganciclovir. Cancer Res., 54:5408-5413.
19. 6, Biotin and C. P.S.E.B.M., 202:265-270.
20. Miller, A.D. and Rosman, G.J. (1989). Improved retroviral vectors for gene transfer and expression. Biotechniques, 7:980-990, 1989.
21. van Osdol, W.W., Sung, C., Dedrick, R.L., and Weinstein, J.N. (1993). A distributed pharmocokinetic model of two-step imaging and treatment of protocols: application to streptavidin-conjugated monoclonal antibodies and radiolabeled biotin. J. Nucl. Med. 34:1552-1564.
22. Paganelli, G., Malcovati, M., and Fazio, F. (1991). Monoclonal antibody pretargeting techniques for tumor localizations: the avidin-biolin system. Nucl. Med. Comm. 12:211-234.
23. Paganelli, G., Pervez, S., et al. (1990). Intraperitoneal radiolocalization of tumors pre-targeted by biotinylated monoclonal antibodies. Int. J. Cancer, 45:1184-1189.
24. Puck, T.T., et al. (1958). Genetics of somatic mammalian cells. III. Long-term cultivation of euploid cells from human and animal subjects. J. Exp. Med. 108:945-956.
25. Ram, Z., Culver, K.W., Walbridge, S., Blaese, R.M. and Oldfield, E.H. (1993). In situ retroviral-mediated gene transfer for the treatment of brain tumors in rats. Cancer Research, 53:83-88.
26. Sorscher, E.J. and Logan, J. Gene therapy for cystic fibrosis using cationic liposome mediated gene transfer: a phase I trial of safety and efficacy in the nasal airway. Human Gene Therapy 5:1259-1277, 1994.
27. Vile, R.G., and Hart, I.R. (1993). Use of tissue-specific expression of the herpes simplex virus thymidine kinase gene to inhibit growth of established murine melanomas following direct intratumoral injection of DNA. Cancer Research, 53:3860-3864.
28. Vile, R.G. and Hart, R.A. (1993). In vitro and in vivo targeting of gene expression to melanoma cells. Cancer Research, 53:962-967.
29. 134.5 deletion mutants in rodent models. J. Clin. Invest., 91:2837-2843.
30. Wolff, J.A., Editor, Gene Therapeutics, Birkhauser Boston, 1993.
31. Zhu, N., Liggitt, D., Liu, Y. and Debs, R. (1993). Systemic gene expression after intravenous DNA delivery into adult mice. Science, 261:209-11.
32. Bebok, Z., Dong, J., Logan, J., King, S., Felgner, P., Kirk, K., Berta, G., Burgess, S., Shaw, W., and Sorscher, E.J. (1994). Plasmid delivery is not a limiting factor in lipid mediated gene transfer in vitro. Ped. Pulm. Suppl., 10:223.
33. Harlow, E., and Lane, D. (1988). Labeling Antibodies, Cold Spring Harbor: Laboratory Manual, 9:321.
34. Bayer, E.A., and Wilchek, M. (1992). Avidin-Biotin Technology. In Methods in Molecular Biology (Immunochemical Protocols)., ed. M. Manson, New Jersey: Humana Press, 14:143-148.