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CHEMICAL DRUG-ASSISTED GENE TRANSFER: A SENSIBLE APPROACH TO IMPROVE TRANSGENE EXPRESSION IN THE CENTRAL NERVOUS SYSTEM GUO HAIYAN NATIONAL UNIVERSITY OF SINGAPORE 2006 CHEMICAL DRUG-ASSISTED GENE TRANSFER: A SENSIBLE APPROACH TO IMPROVE TRANSGENE EXPRESSION IN THE CENTRAL NERVOUS SYSTEM GUO HAIYAN (B.M., PRC) A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF PHILOSOPHY DEPARTMENT OF BIOLOGICAL SCIENCES NATIONAL UNIVERSITY OF SINGAPORE & INSTITUTE OF BIOENGINEERING AND NANOTECHNOLOGY 2006 ACKNOWLEDGMENT I would like to express my sincere thanks and appreciation to my supervisor A/P Wang Shu, for his full support, invaluable guidance, and excellent advice on my research work, as well as his kind understanding and encouragement during my depression period when my work was not going well Without his great help my work would not be done smoothly I also want to sincerely thank my co-supervisor, A/P Lim Tit Meng, for his invaluable support, suggestions and encouragement on my research projects, and for his bright and optimistic smiles which really relieved my stress and strengthened my confidence My sincere thanks also go to A/P Sheu Fwu Shan and Dr Lim Kah Leong, for their sparking ideas and suggestions in our journal club which benefit me a lot Also I would sincerely thank all my dear lab members in IBN and DBS labs for their support and contributions to my work, especially Dr Jurvansuu Jaana, who is my excellent consultant on my experiments and thesis writing; also Dr Wang Xu, Dr Tang Guping, Dr Wang Chaoyang for their special technique support on my projects; and Dr The Hui Leng Christina, who is always there helping around and fully supports me without any hesitation; and Dr Leong Sai Mum who is always giving me valuable advice on my experiments and thesis I I would like to thank my dear parents and husband, who are always standing behind supporting and encouraging me, and whatever they could to help me Special thanks also go to my other friends in NUS and IBN for their kind concerns and moral support II PUBLICATIONS International journals Guo, H Y., S Wang “Enhanced Baculovirus-Mediated p53 Gene Therapy by A Histone Deacetylase Inhibitor, Sodium Butyrate, for Glioblastoma.” (manuscript) Guo, H Y., J M Zeng, W M Fan, S Wang “Downregualtion of Multidrug Transporter P-Glycoprotein Increases Polyethylenimine-Mediated Gene Expression in Tumor Cells.” (manuscript) Wang, C Y., F Li, Y Yang, H Y Guo, C X Wu and S Wang (2006) "Recombinant baculovirus containing the diphtheria toxin A gene for malignant glioma therapy." Cancer Res 66(11): 5798-806 Tang, G P., H Y Guo, F Alexis, X Wang, S Zeng, T M Lim, J Ding, Y Y Yang and S Wang (2006) "Low molecular weight polyethylenimines linked by beta-cyclodextrin for gene transfer into the nervous system." J Gene Med 8(6): 736-44 Wang, C Y., H Y Guo, T M Lim, Y K Ng, H P Neo, P Y Hwang, W C Yee and S Wang (2005) "Improved neuronal transgene expression from an AAV-2 vector with a hybrid CMV enhancer/PDGF-beta promoter." J Gene Med 7(7): 945-55 III Li, Y., X Wang, H Y Guo and S Wang (2004) "Axonal transport of recombinant baculovirus vectors." Mol Ther 10(6): 1121-9 Conferences Guo, H Y., S Wang Enhanced Baculovirus Mediated Gene Therapy by Histone Deacetylase Inhibitor for Glioma (oral presentation) Institute of Bioengineering &Nanotechnology Postgraduate Student Symposium, June 2006, Singapore Guo, H Y., J M Zeng, W M Fan, S Wang Downregulation of Multidrug Transporter P-glycoprotein Increases Polyethylenimine-mediated Gene Expression in Tumor Cells (Poster) Institute of Bioengineering &Nanotechnology Research Symposium, September 2005, Singapore Guo, H Y., C Y Wang, S Wang Neuronal Specific Gene Delivery with A Chimeric CMV IE/PDGF Promoter in A Rat Model (Poster) The 4th Sino-Singapore Conference in Biotechnology November 2003, Singapore Guo, H Y., C Y Wang, S Wang Neuronal Specific Gene Delivery with A Chimeric CMV IE/PDGF Promoter in A Rat Model (Oral Presentation) 8th Biological Sciences Graduate Congress December 2003, Singapore IV CONTENTS PAGE ACKNOWLEDGEMENT I PUBLICATIONS III TABLE OF CONTENTS V SUMMARY IX LIST OF FIGURES XI ABBREVIATION XIII Chapter Introduction 1.1 Current progress in gene therapy 1.2 Gene delivery vectors in central nervous system (CNS) 1.2.1 Non-viral vectors 1.2.1.1 Naked DNA 1.2.1.2 Cationic lipids 1.2.1.3 Cationic polymers 1.2.1.4 Chemical modifications of PEI to facilitate gene delivery 1.2.1.4.1 Polyethylene glycol (PEG) modified PEI 1.2.1.4.2 Ligands modified PEI 1.2.1.4.3 Cross-linking of PEI 10 1.2.1.5 PEI-mediated gene delivery to tumor cells 1.2.2 Viral vectors 1.2.2.1 Adenovirus (Ad) 13 17 18 V 1.2.2.2 Adeno-associated virus (AAV) 18 1.2.2.3 Retrovirus 19 1.2.2.4 Baculovirus 19 1.2.3 Epigenetic gene regulation by chemical compounds, histone deacetylase inhibitors 1.3 Objective of current study 22 24 Chapter Low Molecular Weight Polyethylenimines Modified by β-Cyclodextrin for Improved Gene Delivery 27 2.1 Introduction 28 2.2 Materials and Methods 30 2.2.1 Materials 31 2.2.2 Preparation of PEI 600-CyD copolymer 31 2.2.3 Reporter plasmid and polymer /DNA complexes 31 2.2.4 MTT cytotoxicity assay 32 2.2.5 Gene transfection assay 32 2.3 Results 2.3.1 Effects of PEI600-CyD copolymer on cell survival 35 35 2.3.2 Gene expression mediated by PEI600-CyD copolymer In vitro 35 2.3.3 Gene expression mediated by PEI600-CyD copolymer In vivo 2.4 Discussion 35 43 Chapter Down-regulation of P-Glycoprotein Increases VI Polyethylenimine-mediated Gene Expression 50 3.1 Introduction 51 3.2 Materials and Methods 55 3.2.1 Cell lines and culture 55 3.2.2 Preparation of PEI/DNA complexes 56 3.2.3 Gene delivery in vitro and luciferase activity assay 56 3.2.4 Rhodamine efflux analysis 57 3.2.5 siRNA preparation and transfection 57 3.2.6 Reverse transcription-polymerase chain reaction (RT-PCR) 58 3.2.7 Western blotting 58 3.3 Results 59 3.3.1 Effect of verapamil on PEI-mediated gene delivery in drug resistant tumor cell lines 59 3.3.2 PEI-mediated gene delivery in PGP-positive and PGP-negative tumor cells 60 3.3.3 PEI /DNA complexes inhibit rhodamine 123 efflux in PGP-positive tumor cells 61 3.3.4 PEI-mediated gene delivery efficiency in PGP down-regulated tumor cells 62 3.4 Discussion 72 Chapter A Histone Deacetylase Inhibitor Improves Baculovirus-mediated Gene Therapy in Malignant Gliomas 77 4.1 Introduction 78 VII 4.2 Materials and Methods 83 4.2.1 Cell lines and culture 83 4.2.2 Baculovirus vectors 83 4.2.3 Baculovirus transduction 85 4.2.4 Luciferase activity assay 85 4.2.5 Western blotting 86 4.2.6 Immunohistochemistry 86 4.2.7 MTT cytotoxicity assay 87 4.2.8 TUNEL staining 87 4.2.9 Flow cytometry 87 4.2.10 In vivo study 88 4.3 Results 89 4.3.1 Sodium butyrate improved baculovirus-mediated transgene expression in cultured glioma cells 89 4.3.2 Cytotoxicity of baculovirus-mediated p53 and/or sodium butyrate in vitro 93 4.3.3 Apoptosis in U251 cells treated with baculovirus-mediated p53 and /or sodium butyrate 94 4.3.4 Enhanced antitumor effect in vivo by combination of and sodium butyrate therapy 96 4.4 Discussion 115 Chapter Concusion 126 Chapter References 131 VIII Chapter References Blessing, T., Kursa, M., Holzhauser, R., Kircheis, R., and Wagner, E (2001) Different strategies for formation of pegylated EGF-conjugated PEI/DNA complexes for targeted gene delivery Bioconjug Chem 12, 529-537 Boussif, O., Lezoualc'h, F., Zanta, M A., Mergny, M D., Scherman, D., Demeneix, B., and Behr, J P (1995) A versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimine Proc Natl Acad Sci U S A 92, 7297-7301 Boussif, O., Zanta, M A., and Behr, J P (1996) Optimized galenics improve in vitro gene transfer with cationic molecules up to 1000-fold Gene Ther 3, 1074-1080 Boyce, F M., and Bucher, N L (1996) Baculovirus-mediated gene transfer into mammalian cells Proc Natl Acad Sci U S A 93, 2348-2352 Bucana, C D., Giavazzi, R., Nayar, R., O'Brian, C A., Seid, C., Earnest, L E., and Fan, D (1990) Retention of vital dyes correlates inversely with the multidrug-resistant phenotype of adriamycin-selected murine fibrosarcoma variants Exp Cell Res 190, 69-75 Carson, M J., and Sutcliffe, J G (1999) Balancing function vs self defense: the CNS as an active regulator of immune responses J Neurosci Res 55, 1-8 Cascallo, M., Calbo, J., Capella, G., Fillat, C., Pastor-Anglada, M., and Mazo, A (2005) Enhancement of gemcitabine-induced apoptosis by restoration of p53 function in human pancreatic tumors Oncology 68, 179-189 Chan, H S., DeBoer, G., Thiessen, J J., Budning, A., Kingston, J E., O'Brien, J M., Koren, G., Giesbrecht, E., Haddad, G., Verjee, Z., et al (1996) Combining cyclosporin with chemotherapy controls intraocular retinoblastoma without requiring radiation Clin Cancer Res 2, 1499-1508 Chen, G., Wang, B B., Li, F J., Liu, D Y., Zhou, J F., Lu, Y P., and Ma, D (2005) [Enhancive effect of histone deacetylase inhibitor trichostatin a on transfection efficiency of adenovirus in ovarian carcinoma cell line A2780] Ai Zheng 24, 1196-1200 Chopin, V., Toillon, R A., Jouy, N., and Le Bourhis, X (2002) Sodium butyrate induces P53-independent, Fas-mediated apoptosis in MCF-7 human breast cancer cells Br J Pharmacol 135, 79-86 Clark, P R., Stopeck, A T., Parker, S E., and Hersh, E M (2000) Cationic lipid gene transfer of an IL-2 transgene leads to activation of natural killer cells in a SCID mouse human tumor xenograft Cell Immunol 204, 96-104 Coll, J L., Chollet, P., Brambilla, E., Desplanques, D., Behr, J P., and Favrot, M (1999) In vivo delivery to tumors of DNA complexed with linear polyethylenimine Hum Gene Ther 10, 1659-1666 131 Chapter References Condreay, J P., Witherspoon, S M., Clay, W C., and Kost, T A (1999) Transient and stable gene expression in mammalian cells transduced with a recombinant baculovirus vector Proc Natl Acad Sci U S A 96, 127-132 Costantini, L C., Bakowska, J C., Breakefield, X O., and Isacson, O (2000) Gene therapy in the CNS Gene Ther 7, 93-109 Croyle, M A., Roessler, B J., Hsu, C P., Sun, R., and Amidon, G L (1998) Beta cyclodextrins enhance adenoviral-mediated gene delivery to the intestine Pharm Res 15, 1348-1355 Dachs, G U., Dougherty, G J., Stratford, I J., and Chaplin, D J (1997) Targeting gene therapy to cancer: a review Oncol Res 9, 313-325 Davidson, B L., Allen, E D., Kozarsky, K F., Wilson, J M., and Roessler, B J (1993) A model system for in vivo gene transfer into the central nervous system using an adenoviral vector Nat Genet 3, 219-223 Davis, M E (2002) Non-viral gene delivery systems Curr Opin Biotechnol 13, 128-131 Davis, M E., and Brewster, M E (2004) Cyclodextrin-based pharmaceutics: past, present and future Nat Rev Drug Discov 3, 1023-1035 Demeule, M., Shedid, D., Beaulieu, E., Del Maestro, R F., Moghrabi, A., Ghosn, P B., Moumdjian, R., Berthelet, F., and Beliveau, R (2001) Expression of multidrug-resistance P-glycoprotein (MDR1) in human brain tumors Int J Cancer 93, 62-66 Dorigo, O., Turla, S T., Lebedeva, S., and Gjerset, R A (1998) Sensitization of rat glioblastoma multiforme to cisplatin in vivo following restoration of wild-type p53 function J Neurosurg 88, 535-540 Engelhard, H H., Duncan, H A., Kim, S., Criswell, P S., and Van Eldik, L (2001) Therapeutic effects of sodium butyrate on glioma cells in vitro and in the rat C6 glioma model Neurosurgery 48, 616-624; discussion 624-615 Factor, P (2001) Gene therapy for acute diseases Mol Ther 4, 515-524 Feller, N., Kuiper, C M., Lankelma, J., Ruhdal, J K., Scheper, R J., Pinedo, H M., and Broxterman, H J (1995) Functional detection of MDR1/P170 and MRP/P190-mediated multidrug resistance in tumour cells by flow cytometry Br J Cancer 72, 543-549 Finnin, M S., Donigian, J R., Cohen, A., Richon, V M., Rifkind, R A., Marks, P A., Breslow, R., and Pavletich, N P (1999) Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors Nature 401, 188-193 Fischer, D., Bieber, T., Li, Y., Elsasser, H P., and Kissel, T (1999) A novel non-viral vector for DNA delivery based on low molecular weight, branched 132 Chapter References polyethylenimine: effect of molecular weight on transfection efficiency and cytotoxicity Pharm Res 16, 1273-1279 Forrest, M L., Koerber, J T., and Pack, D W (2003) A degradable polyethylenimine derivative with low toxicity for highly efficient gene delivery Bioconjug Chem 14, 934-940 Forrest, M L., Gabrielson, N., and Pack, D W (2005) Cyclodextrin-polyethylenimine conjugates for targeted in vitro gene delivery Biotechnol Bioeng 89, 416-423 Fujiwara, T., Grimm, E A., Mukhopadhyay, T., Zhang, W W., Owen-Schaub, L B., and Roth, J A (1994) Induction of chemosensitivity in human lung cancer cells in vivo by adenovirus-mediated transfer of the wild-type p53 gene Cancer Res 54, 2287-2291 Gallardo, D., Drazan, K E., and McBride, W H (1996) Adenovirus-based transfer of wild-type p53 gene increases ovarian tumor radiosensitivity Cancer Res 56, 4891-4893 Germann, U A (1996) P-glycoprotein a mediator of multidrug resistance in tumour cells Eur J Cancer 32A, 927-944 Girardin, F (2006) Membrane transporter proteins: a challenge for CNS drug development Dialogues Clin Neurosci 8, 311-321 Glick, R D., Swendeman, S L., Coffey, D C., Rifkind, R A., Marks, P A., Richon, V M., and La Quaglia, M P (1999) Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma Cancer Res 59, 4392-4399 Godbey, W T., Wu, K K., and Mikos, A G (1999a) Poly(ethylenimine) and its role in gene delivery J Control Release 60, 149-160 Godbey, W T., Wu, K K., and Mikos, A G (1999b) Size matters: molecular weight affects the efficiency of poly(ethylenimine) as a gene delivery vehicle J Biomed Mater Res 45, 268-275 Godbey, W T., Wu, K K., and Mikos, A G (1999c) Tracking the intracellular path of poly(ethylenimine)/DNA complexes for gene delivery Proc Natl Acad Sci U S A 96, 5177-5181 Godbey, W T., Wu, K K., and Mikos, A G (2001) Poly(ethylenimine)-mediated gene delivery affects endothelial cell function and viability Biomaterials 22, 471-480 Gomez-Manzano, C., Fueyo, J., Kyritsis, A P., Steck, P A., Roth, J A., McDonnell, T J., Steck, K D., Levin, V A., and Yung, W K (1996) Adenovirus-mediated transfer of the p53 gene produces rapid and generalized death of human glioma cells via apoptosis Cancer Res 56, 694-699 133 Chapter References Gonzalez, H., Hwang, S J., and Davis, M E (1999) New class of polymers for the delivery of macromolecular therapeutics Bioconjug Chem 10, 1068-1074 Gosselin, M A., Guo, W., and Lee, R J (2001) Efficient gene transfer using reversibly cross-linked low molecular weight polyethylenimine Bioconjug Chem 12, 989-994 Gottesman, M M., Fojo, T., and Bates, S E (2002) Multidrug resistance in cancer: role of ATP-dependent transporters Nat Rev Cancer 2, 48-58 Goula, D., Remy, J S., Erbacher, P., Wasowicz, M., Levi, G., Abdallah, B., and Demeneix, B A (1998) Size, diffusibility and transfection performance of linear PEI/DNA complexes in the mouse central nervous system Gene Ther 5, 712-717 Grzelinski, M., Urban-Klein, B., Martens, T., Lamszus, K., Bakowsky, U., Hobel, S., Czubayko, F., and Aigner, A (2006) RNA interference-mediated gene silencing of pleiotrophin through polyethylenimine-complexed small interfering RNAs in vivo exerts antitumoral effects in glioblastoma xenografts Hum Gene Ther 17, 751-766 Gupta, M., Fan, S., Zhan, Q., Kohn, K W., O'Connor, P M., and Pommier, Y (1997) Inactivation of p53 increases the cytotoxicity of camptothecin in human colon HCT116 and breast MCF-7 cancer cells Clin Cancer Res 3, 1653-1660 Harsh, G R., Deisboeck, T S., Louis, D N., Hilton, J., Colvin, M., Silver, J S., Qureshi, N H., Kracher, J., Finkelstein, D., Chiocca, E A., and Hochberg, F H (2000) Thymidine kinase activation of ganciclovir in recurrent malignant gliomas: a gene-marking and neuropathological study J Neurosurg 92, 804-811 Hawkins, D S., Demers, G W., and Galloway, D A (1996) Inactivation of p53 enhances sensitivity to multiple chemotherapeutic agents Cancer Res 56, 892-898 Hofmann, C., Sandig, V., Jennings, G., Rudolph, M., Schlag, P., and Strauss, M (1995) Efficient gene transfer into human hepatocytes by baculovirus vectors Proc Natl Acad Sci U S A 92, 10099-10103 Hofmann, C., and Strauss, M (1998) Baculovirus-mediated gene transfer in the presence of human serum or blood facilitated by inhibition of the complement system Gene Ther 5, 531-536 Horne, R W., Ronchetti, I P., and Hobart, J M (1975) A negative staining-carbon film technique for studying viruses in the electron microscope II Application to adenovirus type J Ultrastruct Res 51, 233-252 Hsich, G., Sena-Esteves, M., and Breakefield, X O (2002) Critical issues in gene therapy for neurologic disease Hum Gene Ther 13, 579-604 134 Chapter References Hu, Y C., Tsai, C T., Chang, Y J., and Huang, J H (2003) Enhancement and prolongation of baculovirus-mediated expression in mammalian cells: focuses on strategic infection and feeding Biotechnol Prog 19, 373-379 Hu, Y C (2005) Baculovirus as a highly efficient expression vector in insect and mammalian cells Acta Pharmacol Sin 26, 405-416 Hwang, S J., Bellocq, N C., and Davis, M E (2001) Effects of structure of beta-cyclodextrin-containing polymers on gene delivery Bioconjug Chem 12, 280-290 Imaoka, T., Date, I., Ohmoto, T., Yasuda, T., and Tsuda, M (1998) In vivo gene transfer into the adult mammalian central nervous system by continuous injection of plasmid DNA-cationic liposome complex Brain Res 780, 119-128 Immonen, A., Vapalahti, M., Tyynela, K., Hurskainen, H., Sandmair, A., Vanninen, R., Langford, G., Murray, N., and Yla-Herttuala, S (2004) AdvHSV-tk gene therapy with intravenous ganciclovir improves survival in human malignant glioma: a randomised, controlled study Mol Ther 10, 967-972 Inoue, A., Narumi, K., Matsubara, N., Sugawara, S., Saijo, Y., Satoh, K., and Nukiwa, T (2000) Administration of wild-type p53 adenoviral vector synergistically enhances the cytotoxicity of anti-cancer drugs in human lung cancer cells irrespective of the status of p53 gene Cancer Lett 157, 105-112 Insinga, A., Monestiroli, S., Ronzoni, S., Gelmetti, V., Marchesi, F., Viale, A., Altucci, L., Nervi, C., Minucci, S., and Pelicci, P G (2005) Inhibitors of histone deacetylases induce tumor-selective apoptosis through activation of the death receptor pathway Nat Med 11, 71-76 Ito, N., Sawa, H., Nagane, M., Noguchi, A., Hara, M., and Saito, I (2001) Inhibitory effects of sodium butyrate on proliferation and invasiveness of human glioma cells Neurosurgery 49, 430-436; discussion 436-437 Jackson, C A., Cobbs, C., Peduzzi, J D., Novak, M., and Morrow, C D (2001) Repetitive intrathecal injections of poliovirus replicons result in gene expression in neurons of the central nervous system without pathogenesis Hum Gene Ther 12, 1827-1841 Johnstone, R W (2002) Histone-deacetylase inhibitors: novel drugs for the treatment of cancer Nat Rev Drug Discov 1, 287-299 Kichler, A., Chillon, M., Leborgne, C., Danos, O., and Frisch, B (2002) Intranasal gene delivery with a polyethylenimine-PEG conjugate J Control Release 81, 379-388 Kichler, A (2004) Gene transfer with modified polyethylenimines J Gene Med Suppl 1, S3-10 135 Chapter References Kircheis, R., Kichler, A., Wallner, G., Kursa, M., Ogris, M., Felzmann, T., Buchberger, M., and Wagner, E (1997) Coupling of cell-binding ligands to polyethylenimine for targeted gene delivery Gene Ther 4, 409-418 Kircheis, R., Schuller, S., Brunner, S., Ogris, M., Heider, K H., Zauner, W., and Wagner, E (1999) Polycation-based DNA complexes for tumor-targeted gene delivery in vivo J Gene Med 1, 111-120 Kircheis, R., Wightman, L., Schreiber, A., Robitza, B., Rossler, V., Kursa, M., and Wagner, E (2001a) Polyethylenimine/DNA complexes shielded by transferrin target gene expression to tumors after systemic application Gene Ther 8, 28-40 Kircheis, R., Wightman, L., and Wagner, E (2001b) Design and gene delivery activity of modified polyethylenimines Adv Drug Deliv Rev 53, 341-358 Kitazono, M., Goldsmith, M E., Aikou, T., Bates, S., and Fojo, T (2001) Enhanced adenovirus transgene expression in malignant cells treated with the histone deacetylase inhibitor FR901228 Cancer Res 61, 6328-6330 Kitazono, M., Rao, V K., Robey, R., Aikou, T., Bates, S., Fojo, T., and Goldsmith, M E (2002) Histone deacetylase inhibitor FR901228 enhances adenovirus infection of hematopoietic cells Blood 99, 2248-2251 Komata, T., Kondo, Y., Kanzawa, T., Hirohata, S., Koga, S., Sumiyoshi, H., Srinivasula, S M., Barna, B P., Germano, I M., Takakura, M., et al (2001) Treatment of malignant glioma cells with the transfer of constitutively active caspase-6 using the human telomerase catalytic subunit (human telomerase reverse transcriptase) gene promoter Cancer Res 61, 5796-5802 Kondo, S., Barna, B P., Kondo, Y., Tanaka, Y., Casey, G., Liu, J., Morimura, T., Kaakaji, R., Peterson, J W., Werbel, B., and Barnett, G H (1996) WAF1/CIP1 increases the susceptibility of p53 non-functional malignant glioma cells to cisplatin-induced apoptosis Oncogene 13, 1279-1285 Kong, J X., Song, Q., Liu, Y P., Wang, C W., and Zhang, Q L (2005) [Inhibition of multidrug resistance gene expression in glioma by antisense oligodeoxynucleotides] Zhongguo Yi Xue Ke Xue Yuan Xue Bao 27, 211-215 Kost, T A., and Condreay, J P (2002) Recombinant baculoviruses as mammalian cell gene-delivery vectors Trends Biotechnol 20, 173-180 Kost, T A., Condreay, J P., and Jarvis, D L (2005) Baculovirus as versatile vectors for protein expression in insect and mammalian cells Nat Biotechnol 23, 567-575 Krishna, R., and Mayer, L D (2000) Multidrug resistance (MDR) in cancer Mechanisms, reversal using modulators of MDR and the role of MDR modulators in influencing the pharmacokinetics of anticancer drugs Eur J Pharm Sci 11, 265-283 136 Chapter References Kursa, M., Walker, G F., Roessler, V., Ogris, M., Roedl, W., Kircheis, R., and Wagner, E (2003) Novel shielded transferrin-polyethylene glycol-polyethylenimine/DNA complexes for systemic tumor-targeted gene transfer Bioconjug Chem 14, 222-231 Kwon, S H., Ahn, S H., Kim, Y K., Bae, G U., Yoon, J W., Hong, S., Lee, H Y., Lee, Y W., Lee, H W., and Han, J W (2002) Apicidin, a histone deacetylase inhibitor, induces apoptosis and Fas/Fas ligand expression in human acute promyelocytic leukemia cells J Biol Chem 277, 2073-2080 Lang, F F., Yung, W K., Sawaya, R., and Tofilon, P J (1999) Adenovirus-mediated p53 gene therapy for human gliomas Neurosurgery 45, 1093-1104 Lawrencia, C., Mahendran, R., and Esuvaranathan, K (2001) Transfection of urothelial cells using methyl-beta-cyclodextrin solubilized cholesterol and Dotap Gene Ther 8, 760-768 Lebherz, C., Auricchio, A., Maguire, A M., Rivera, V M., Tang, W., Grant, R L., Clackson, T., Bennett, J., and Wilson, J M (2005) Long-term inducible gene expression in the eye via adeno-associated virus gene transfer in nonhuman primates Hum Gene Ther 16, 178-186 Lee, G., and Bendayan, R (2004) Functional expression and localization of P-glycoprotein in the central nervous system: relevance to the pathogenesis and treatment of neurological disorders Pharm Res 21, 1313-1330 Lehtolainen, P., Tyynela, K., Kannasto, J., Airenne, K J., and Yla-Herttuala, S (2002) Baculoviruses exhibit restricted cell type specificity in rat brain: a comparison of baculovirus- and adenovirus-mediated intracerebral gene transfer in vivo Gene Ther 9, 1693-1699 Li, H., Lochmuller, H., Yong, V W., Karpati, G., and Nalbantoglu, J (1997) Adenovirus-mediated wild-type p53 gene transfer and overexpression induces apoptosis of human glioma cells independent of endogenous p53 status J Neuropathol Exp Neurol 56, 872-878 Li, H., Alonso-Vanegas, M., Colicos, M A., Jung, S S., Lochmuller, H., Sadikot, A F., Snipes, G J., Seth, P., Karpati, G., and Nalbantoglu, J (1999) Intracerebral adenovirus-mediated p53 tumor suppressor gene therapy for experimental human glioma Clin Cancer Res 5, 637-642 Li, Y., Wang, X., Guo, H., and Wang, S (2004) Axonal transport of recombinant baculovirus vectors Mol Ther 10, 1121-1129 Li, Y., Yang, Y., and Wang, S (2005) Neuronal gene transfer by baculovirus-derived vectors accommodating a neurone-specific promoter Exp Physiol 90, 39-44 Lim, Y B., Han, S O., Kong, H U., Lee, Y., Park, J S., Jeong, B., and Kim, S W (2000) Biodegradable polyester, poly[alpha-(4-aminobutyl)-L-glycolic acid], as a non-toxic gene carrier Pharm Res 17, 811-816 137 Chapter References Liu, Y., Liggitt, D., Fong, S., and Debs, R J (2006) Systemic co-administration of depsipeptide selectively targets transfection enhancement to specific tissues and cell types Gene Ther Lowe, S W., Ruley, H E., Jacks, T., and Housman, D E (1993) p53-dependent apoptosis modulates the cytotoxicity of anticancer agents Cell 74, 957-967 Ludescher, C., Gattringer, Drach, J., Hofmann, J., and Grunicke, H (1991) Rapid functional assay for the detection of multidrug-resistant cells using the fluorescent dye rhodamine 123 Blood 78, 1385-1387 Lungwitz, U., Breunig, M., Blunk, T., and Gopferich, A (2005) Polyethylenimine-based non-viral gene delivery systems Eur J Pharm Biopharm 60, 247-266 Lusky, M., Christ, M., Rittner, K., Dieterle, A., Dreyer, D., Mourot, B., Schultz, H., Stoeckel, F., Pavirani, A., and Mehtali, M (1998) In vitro and in vivo biology of recombinant adenovirus vectors with E1, E1/E2A, or E1/E4 deleted J Virol 72, 2022-2032 Mahato, R I., Rolland, A., and Tomlinson, E (1997) Cationic lipid-based gene delivery systems: pharmaceutical perspectives Pharm Res 14, 853-859 Martino, G., Furlan, R., Comi, G., and Adorini, L (2001) The ependymal route to the CNS: an emerging gene-therapy approach for MS Trends Immunol 22, 483-490 Merdan, T., Kopecek, J., and Kissel, T (2002) Prospects for cationic polymers in gene and oligonucleotide therapy against cancer Adv Drug Deliv Rev 54, 715-758 Merrihew, R V., Clay, W C., Condreay, J P., Witherspoon, S M., Dallas, W S., and Kost, T A (2001) Chromosomal integration of transduced recombinant baculovirus DNA in mammalian cells J Virol 75, 903-909 Meuli-Simmen, C., Liu, Y., Yeo, T T., Liggitt, D., Tu, G., Yang, T., Meuli, M., Knauer, S., Heath, T D., Longo, F M., and Debs, R J (1999) Gene expression along the cerebral-spinal axis after regional gene delivery Hum Gene Ther 10, 2689-2700 Moffatt, S., Wiehle, S., and Cristiano, R J (2005) Tumor-specific gene delivery mediated by a novel peptide-polyethylenimine-DNA polyplex targeting aminopeptidase N/CD13 Hum Gene Ther 16, 57-67 Moghimi, S M., Symonds, P., Murray, J C., Hunter, A C., Debska, G., and Szewczyk, A (2005) A two-stage poly(ethylenimine)-mediated cytotoxicity: implications for gene transfer/therapy Mol Ther 11, 990-995 Nebbioso, A., Clarke, N., Voltz, E., Germain, E., Ambrosino, C., Bontempo, P., Alvarez, R., Schiavone, E M., Ferrara, F., Bresciani, F., et al (2005) 138 Chapter References Tumor-selective action of HDAC inhibitors involves TRAIL induction in acute myeloid leukemia cells Nat Med 11, 77-84 Neu, M., Fischer, D., and Kissel, T (2005) Recent advances in rational gene transfer vector design based on poly(ethylene imine) and its derivatives J Gene Med 7, 992-1009 Niola, F., Evangelisti, C., Campagnolo, L., Massalini, S., Bue, M C., Mangiola, A., Masotti, A., Maira, G., Farace, M G., and Ciafre, S A (2006) A plasmid-encoded VEGF siRNA reduces glioblastoma angiogenesis and its combination with interleukin-4 blocks tumor growth in a xenograft mouse model Cancer Biol Ther 5, 174-179 Nishizaki, M., Meyn, R E., Levy, L B., Atkinson, E N., White, R A., Roth, J A., and Ji, L (2001) Synergistic inhibition of human lung cancer cell growth by adenovirus-mediated wild-type p53 gene transfer in combination with docetaxel and radiation therapeutics in vitro and in vivo Clin Cancer Res 7, 2887-2897 O'Connor, P M., Jackman, J., Bae, I., Myers, T G., Fan, S., Mutoh, M., Scudiero, D A., Monks, A., Sausville, E A., Weinstein, J N., et al (1997) Characterization of the p53 tumor suppressor pathway in cell lines of the National Cancer Institute anticancer drug screen and correlations with the growth-inhibitory potency of 123 anticancer agents Cancer Res 57, 4285-4300 Ogris, M., Steinlein, P., Kursa, M., Mechtler, K., Kircheis, R., and Wagner, E (1998) The size of DNA/transferrin-PEI complexes is an important factor for gene expression in cultured cells Gene Ther 5, 1425-1433 Ogris, M., Brunner, S., Schuller, S., Kircheis, R., and Wagner, E (1999) PEGylated DNA/transferrin-PEI complexes: reduced interaction with blood components, extended circulation in blood and potential for systemic gene delivery Gene Ther 6, 595-605 Ogris, M., Walker, G., Blessing, T., Kircheis, R., Wolschek, M., and Wagner, E (2003) Tumor-targeted gene therapy: strategies for the preparation of ligand-polyethylene glycol-polyethylenimine/DNA complexes J Control Release 91, 173-181 Okada, T., Uchibori, R., Iwata-Okada, M., Takahashi, M., Nomoto, T., Nonaka-Sarukawa, M., Ito, T., Liu, Y., Mizukami, H., Kume, A., et al (2006) A histone deacetylase inhibitor enhances recombinant adeno-associated virus-mediated gene expression in tumor cells Mol Ther 13, 738-746 Okegawa, T., Nutahara, K., Pong, R C., Higashihara, E., and Hsieh, J T (2005) Enhanced transgene expression in urothelial cancer gene therapy with histone deacetylase inhibitor J Urol 174, 747-752 Osaki, S., Nakanishi, Y., Takayama, K., Pei, X H., Ueno, H., and Hara, N (2000) Alteration of drug chemosensitivity caused by the adenovirus-mediated 139 Chapter References transfer of the wild-type p53 gene in human lung cancer cells Cancer Gene Ther 7, 300-307 Ouatas, T., Le Mevel, S., Demeneix, B A., and de Luze, A (1998) T3-dependent physiological regulation of transcription in the Xenopus tadpole brain studied by polyethylenimine based in vivo gene transfer Int J Dev Biol 42, 1159-1164 Palombo, F., Monciotti, A., Recchia, A., Cortese, R., Ciliberto, G., and La Monica, N (1998) Site-specific integration in mammalian cells mediated by a new hybrid baculovirus-adeno-associated virus vector J Virol 72, 5025-5034 Pedroso de Lima, M C., Simoes, S., Pires, P., Faneca, H., and Duzgunes, N (2001) Cationic lipid-DNA complexes in gene delivery: from biophysics to biological applications Adv Drug Deliv Rev 47, 277-294 Petersen, H., Fechner, P M., Martin, A L., Kunath, K., Stolnik, S., Roberts, C J., Fischer, D., Davies, M C., and Kissel, T (2002a) Polyethylenimine-graft-poly(ethylene glycol) copolymers: influence of copolymer block structure on DNA complexation and biological activities as gene delivery system Bioconjug Chem 13, 845-854 Petersen, H., Merdan, T., Kunath, K., Fischer, D., and Kissel, T (2002b) Poly(ethylenimine-co-L-lactamide-co-succinamide): a biodegradable polyethylenimine derivative with an advantageous pH-dependent hydrolytic degradation for gene delivery Bioconjug Chem 13, 812-821 Pun, S H., Bellocq, N C., Liu, A., Jensen, G., Machemer, T., Quijano, E., Schluep, T., Wen, S., Engler, H., Heidel, J., and Davis, M E (2004) Cyclodextrin-modified polyethylenimine polymers for gene delivery Bioconjug Chem 15, 831-840 Puumalainen, A M., Vapalahti, M., Agrawal, R S., Kossila, M., Laukkanen, J., Lehtolainen, P., Viita, H., Paljarvi, L., Vanninen, R., and Yla-Herttuala, S (1998) Beta-galactosidase gene transfer to human malignant glioma in vivo using replication-deficient retroviruses and adenoviruses Hum Gene Ther 9, 1769-1774 Rabinowitz, J E., and Samulski, J (1998) Adeno-associated virus expression systems for gene transfer Curr Opin Biotechnol 9, 470-475 Rainov, N G (2000) A phase III clinical evaluation of herpes simplex virus type thymidine kinase and ganciclovir gene therapy as an adjuvant to surgical resection and radiation in adults with previously untreated glioblastoma multiforme Hum Gene Ther 11, 2389-2401 Ram, Z., Walbridge, S., Oshiro, E M., Viola, J J., Chiang, Y., Mueller, S N., Blaese, R M., and Oldfield, E H (1994) Intrathecal gene therapy for malignant leptomeningeal neoplasia Cancer Res 54, 2141-2145 Ramachandra, M., Ambudkar, S V., Chen, D., Hrycyna, C A., Dey, S., Gottesman, M M., and Pastan, I (1998) Human P-glycoprotein exhibits 140 Chapter References reduced affinity for substrates during a catalytic transition state Biochemistry 37, 5010-5019 Rao, V V., Dahlheimer, J L., Bardgett, M E., Snyder, A Z., Finch, R A., Sartorelli, A C., and Piwnica-Worms, D (1999) Choroid plexus epithelial expression of MDR1 P glycoprotein and multidrug resistance-associated protein contribute to the blood-cerebrospinal-fluid drug-permeability barrier Proc Natl Acad Sci U S A 96, 3900-3905 Raper, S E., Chirmule, N., Lee, F S., Wivel, N A., Bagg, A., Gao, G P., Wilson, J M., and Batshaw, M L (2003) Fatal systemic inflammatory response syndrome in a ornithine transcarbamylase deficient patient following adenoviral gene transfer Mol Genet Metab 80, 148-158 Rieger, L., Rieger, J., Winter, S., Streffer, J., Esser, P., Dichgans, J., Meyermann, R., and Weller, M (2000) Evidence for a constitutive, verapamil-sensitive, non-P-glycoprotein multidrug resistance phenotype in malignant glioma that is unaltered by radiochemotherapy in vivo Acta Neuropathol (Berl) 99, 555-562 Ruefli, A A., Ausserlechner, M J., Bernhard, D., Sutton, V R., Tainton, K M., Kofler, R., Smyth, M J., and Johnstone, R W (2001) The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species Proc Natl Acad Sci U S A 98, 10833-10838 Ruefli, A A., Ausserlechner, M J., Bernhard, D., Sutton, V R., Tainton, K M., Kofler, R., Smyth, M J., and Johnstone, R W (2001) The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species Proc Natl Acad Sci U S A 98, 10833-10838 Saeki, T., Ueda, K., Tanigawara, Y., Hori, R., and Komano, T (1993a) Human P-glycoprotein transports cyclosporin A and FK506 J Biol Chem 268, 6077-6080 Saeki, T., Ueda, K., Tanigawara, Y., Hori, R., and Komano, T (1993b) P-glycoprotein-mediated transcellular transport of MDR-reversing agents FEBS Lett 324, 99-102 Sandmair, A M., Vapalahti, M., and Yla-Herttuala, S (2000) Adenovirus-mediated herpes simplex thymidine kinase gene therapy for brain tumors Adv Exp Med Biol 465, 163-170 Sarkis, C., Serguera, C., Petres, S., Buchet, D., Ridet, J L., Edelman, L., and Mallet, J (2000) Efficient transduction of neural cells in vitro and in vivo by a baculovirus-derived vector Proc Natl Acad Sci U S A 97, 14638-14643 141 Chapter References Sauna, Z E., and Ambudkar, S V (2000) Evidence for a requirement for ATP hydrolysis at two distinct steps during a single turnover of the catalytic cycle of human P-glycoprotein Proc Natl Acad Sci U S A 97, 2515-2520 Schiedner, G., Morral, N., Parks, R J., Wu, Y., Koopmans, S C., Langston, C., Graham, F L., Beaudet, A L., and Kochanek, S (1998) Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity Nat Genet 18, 180-183 Schinkel, A H., Wagenaar, E., Mol, C A., and van Deemter, L (1996) P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs J Clin Invest 97, 2517-2524 Schuldt, C., Zoller, L., Bautz, E K., and Darai, G (1994) Baculovirus expression of the nucleocapsid protein of a Puumala serotype Hantavirus Virus Genes 8, 143-149 Schwartz, B., Benoist, C., Abdallah, B., Rangara, R., Hassan, A., Scherman, D., and Demeneix, B A (1996) Gene transfer by naked DNA into adult mouse brain Gene Ther 3, 405-411 Seelig, A (1998) A general pattern for substrate recognition by P-glycoprotein Eur J Biochem 251, 252-261 Shen, D W., Goldenberg, S., Pastan, I., and Gottesman, M M (2000) Decreased accumulation of [14C]carboplatin in human cisplatin-resistant cells results from reduced energy-dependent uptake J Cell Physiol 183, 108-116 Shi, L., Tang, G P., Gao, S J., Ma, Y X., Liu, B H., Li, Y., Zeng, J M., Ng, Y K., Leong, K W., and Wang, S (2003) Repeated intrathecal administration of plasmid DNA complexed with polyethylene glycol-grafted polyethylenimine led to prolonged transgene expression in the spinal cord Gene Ther 10, 1179-1188 Shir, A., Ogris, M., Wagner, E., and Levitzki, A (2006) EGF receptor-targeted synthetic double-stranded RNA eliminates glioblastoma, breast cancer, and adenocarcinoma tumors in mice PLoS Med 3, e6 Shoji, I., Aizaki, H., Tani, H., Ishii, K., Chiba, T., Saito, I., Miyamura, T., and Matsuura, Y (1997) Efficient gene transfer into various mammalian cells, including non-hepatic cells, by baculovirus vectors J Gen Virol 78 ( Pt 10), 2657-2664 Sidransky, D., Mikkelsen, T., Schwechheimer, K., Rosenblum, M L., Cavanee, W., and Vogelstein, B (1992) Clonal expansion of p53 mutant cells is associated with brain tumour progression Nature 355, 846-847 Song, S U., and Boyce, F M (2001) Combination treatment for osteosarcoma with baculoviral vector mediated gene therapy (p53) and chemotherapy (adriamycin) Exp Mol Med 33, 46-53 142 Chapter References Spiegl-Kreinecker, S., Buchroithner, J., Elbling, L., Steiner, E., Wurm, G., Bodenteich, A., Fischer, J., Micksche, M., and Berger, W (2002) Expression and functional activity of the ABC-transporter proteins P-glycoprotein and multidrug-resistance protein in human brain tumor cells and astrocytes J Neurooncol 57, 27-36 Takimoto, R., Kato, J., Terui, T., Takada, K., Kuroiwa, G., Wu, J., Ohnuma, H., Takahari, D., Kobune, M., Sato, Y., et al (2005) Augmentation of antitumor effects of p53 gene therapy by combination with HDAC inhibitor Cancer Biol Ther 4, 421-428 Tang, G P., Zeng, J M., Gao, S J., Ma, Y X., Shi, L., Li, Y., Too, H P., and Wang, S (2003) Polyethylene glycol modified polyethylenimine for improved CNS gene transfer: effects of PEGylation extent Biomaterials 24, 2351-2362 Terui, T., Murakami, K., Takimoto, R., Takahashi, M., Takada, K., Murakami, T., Minami, S., Matsunaga, T., Takayama, T., Kato, J., and Niitsu, Y (2003) Induction of PIG3 and NOXA through acetylation of p53 at 320 and 373 lysine residues as a mechanism for apoptotic cell death by histone deacetylase inhibitors Cancer Res 63, 8948-8954 Thomas, H., and Coley, H M (2003) Overcoming multidrug resistance in cancer: an update on the clinical strategy of inhibiting p-glycoprotein Cancer Control 10, 159-165 Thomas, M., Ge, Q., Lu, J J., Chen, J., and Klibanov, A M (2005) Cross-linked small polyethylenimines: while still nontoxic, deliver DNA efficiently to mammalian cells in vitro and in vivo Pharm Res 22, 373-380 Trask, T W., Trask, R P., Aguilar-Cordova, E., Shine, H D., Wyde, P R., Goodman, J C., Hamilton, W J., Rojas-Martinez, A., Chen, S H., Woo, S L., and Grossman, R G (2000) Phase I study of adenoviral delivery of the HSV-tk gene and ganciclovir administration in patients with current malignant brain tumors Mol Ther 1, 195-203 Van Meir, E G., Kikuchi, T., Tada, M., Li, H., Diserens, A C., Wojcik, B E., Huang, H J., Friedmann, T., de Tribolet, N., and Cavenee, W K (1994) Analysis of the p53 gene and its expression in human glioblastoma cells Cancer Res 54, 649-652 VandenDriessche, T., Collen, D., and Chuah, M K (2003) Biosafety of onco-retroviral vectors Curr Gene Ther 3, 501-515 Volkman, L E., and Goldsmith, P A (1983) In Vitro Survey of Autographa californica Nuclear Polyhedrosis Virus Interaction with Nontarget Vertebrate Host Cells Appl Environ Microbiol 45, 1085-1093 Vrana, J A., Decker, R H., Johnson, C R., Wang, Z., Jarvis, W D., Richon, V M., Ehinger, M., Fisher, P B., and Grant, S (1999) Induction of apoptosis in U937 human leukemia cells by suberoylanilide hydroxamic acid (SAHA) 143 Chapter References proceeds through pathways that are regulated by Bcl-2/Bcl-XL, c-Jun, and p21CIP1, but independent of p53 Oncogene 18, 7016-7025 Wandel, C., Kim, R B., Kajiji, S., Guengerich, P., Wilkinson, G R., and Wood, A J (1999) P-glycoprotein and cytochrome P-450 3A inhibition: dissociation of inhibitory potencies Cancer Res 59, 3944-3948 Wang, S., Ma, N., Gao, S J., Yu, H., and Leong, K W (2001) Transgene expression in the brain stem effected by intramuscular injection of polyethylenimine/DNA complexes Mol Ther 3, 658-664 Wang, C Y., Guo, H Y., Lim, T M., Ng, Y K., Neo, H P., Hwang, P Y., Yee, W C., and Wang, S (2005) Improved neuronal transgene expression from an AAV-2 vector with a hybrid CMV enhancer/PDGF-beta promoter J Gene Med 7, 945-955 Wang, C Y., Li, F., Yang, Y., Guo, H Y., Wu, C X., and Wang, S (2006) Recombinant baculovirus containing the diphtheria toxin A gene for malignant glioma therapy Cancer Res 66, 5798-5806 Warrell, R P., Jr., He, L Z., Richon, V., Calleja, E., and Pandolfi, P P (1998) Therapeutic targeting of transcription in acute promyelocytic leukemia by use of an inhibitor of histone deacetylase J Natl Cancer Inst 90, 1621-1625 Warrener, R., Beamish, H., Burgess, A., Waterhouse, N J., Giles, N., Fairlie, D., and Gabrielli, B (2003) Tumor cell-selective cytotoxicity by targeting cell cycle checkpoints Faseb J 17, 1550-1552 Weaver, J L., Pine, P S., Aszalos, A., Schoenlein, P V., Currier, S J., Padmanabhan, R., and Gottesman, M M (1991) Laser scanning and confocal microscopy of daunorubicin, doxorubicin, and rhodamine 123 in multidrug-resistant cells Exp Cell Res 196, 323-329 Weber, E., Anderson, W F., and Kasahara, N (2001) Recent advances in retrovirus vector-mediated gene therapy: teaching an old vector new tricks Curr Opin Mol Ther 3, 439-453 Weidle, U H., and Grossmann, A (2000) Inhibition of histone deacetylases: a new strategy to target epigenetic modifications for anticancer treatment Anticancer Res 20, 1471-1485 Wieczorek, A M., Waterman, J L., Waterman, M J., and Halazonetis, T D (1996) Structure-based rescue of common tumor-derived p53 mutants Nat Med 2, 1143-1146 Witherspoon, S M., Emerson, D L., Kerr, B M., Lloyd, T L., Dalton, W S., and Wissel, P S (1996) Flow cytometric assay of modulation of P-glycoprotein function in whole blood by the multidrug resistance inhibitor GG918 Clin Cancer Res 2, 7-12 144 Chapter References Wolff, J A., Malone, R W., Williams, P., Chong, W., Acsadi, G., Jani, A., and Felgner, P L (1990) Direct gene transfer into mouse muscle in vivo Science 247, 1465-1468 Wu, H., Hait, W N., and Yang, J M (2003) Small interfering RNA-induced suppression of MDR1 (P-glycoprotein) restores sensitivity to multidrug-resistant cancer cells Cancer Res 63, 1515-1519 Xiao, X., Li, J., and Samulski, R J (1996) Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector J Virol 70, 8098-8108 Xu, D., McCarty, D., Fernandes, A., Fisher, M., Samulski, R J., and Juliano, R L (2005) Delivery of MDR1 small interfering RNA by self-complementary recombinant adeno-associated virus vector Mol Ther 11, 523-530 Yap, C C., Ishii, K., Aoki, Y., Aizaki, H., Tani, H., Shimizu, H., Ueno, Y., Miyamura, T., and Matsuura, Y (1997) A hybrid baculovirus-T7 RNA polymerase system for recovery of an infectious virus from cDNA Virology 231, 192-200 Yoshida, T., Mizuno, M., Taniguchi, K., Nakayashiki, N., Wakabayashi, T., and Yoshida, J (2001) Rat glioma cell death induced by cationic liposome-mediated transfer of the herpes simplex virus thymidine kinase gene followed by ganciclovir treatment J Surg Oncol 76, 19-25 Yoshida, M., Furumai, R., Nishiyama, M., Komatsu, Y., Nishino, N., and Horinouchi, S (2001) Histone deacetylase as a new target for cancer chemotherapy Cancer Chemother Pharmacol 48 Suppl 1, S20-26 Yoshida, J., and Mizuno, M (2003) Clinical gene therapy for brain tumors Liposomal delivery of anticancer molecule to glioma J Neurooncol 65, 261-267 Yu, Q (2006) Restoring p53-mediated apoptosis in cancer cells: new opportunities for cancer therapy Drug Resist Updat 9, 19-25 Yusa, K., and Tsuruo, T (1989) Reversal mechanism of multidrug resistance by verapamil: direct binding of verapamil to P-glycoprotein on specific sites and transport of verapamil outward across the plasma membrane of K562/ADM cells Cancer Res 49, 5002-5006 Zerrouqi, A., Rixe, O., Ghoumari, A M., Yarovoi, S V., Mouawad, R., Khayat, D., and Soubrane, C (1996) Liposomal delivery of the herpes simplex virus thymidine kinase gene in glioma: improvement of cell sensitization to ganciclovir Cancer Gene Ther 3, 385-392 Zhao, P., Hu, W., Zhang, Y Z., Sun, M Z., and He, Y (2006) [Reversion of multidrug resistance (MDR) in human glioma cells by RNA interference (RNAi)] Zhonghua Zhong Liu Za Zhi 28, 183-187 145 ... these above studies indicate a novel approach to use HDAC inhibitors to enhance baculovirus-mediated gene therapy by increasing the expression of the transgene In addition, with their intrinsic anti-tumor.. .CHEMICAL DRUG- ASSISTED GENE TRANSFER: A SENSIBLE APPROACH TO IMPROVE TRANSGENE EXPRESSION IN THE CENTRAL NERVOUS SYSTEM GUO HAIYAN (B.M., PRC) A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR... or interfere with disease-causing processes(Factor, 2001) The original goal of gene therapy was to correct a genetic disorder by inserting a functional gene into an organism to replace an inherited