Pharmacological Modulation of the Bystander Effect in the Herpes Simplex Virus Thymidine Kinase/Ganciclovir Gene Therapy System: Effects of Dibutyryl Adenosine 3',5'-Cyclic Monophosphate, Alpha-Glycyrrhetinic Acid, and Cytosine Arabinoside
[en] The herpes simplex virus type 1 thymidine kinase (HSV1-tk) suicide gene/ganciclovir system was first applied to the treatment of glioblastoma tumors, but was hampered by the low gene transfection yield. Fortunately, the gap junction-dependent diffusion of phosphorylated ganciclovir metabolites from transfected cells to their neighbors proved to enhance the overall benefit of this strategy. However, as tumor cells are often gap junction-deficient, we sought to restore this property pharmacologically and hence to improve the efficacy of the treatment. We demonstrated that this approach was feasible in glioblastoma cells using dibutyryl adenosine 3',5'-cyclic monophosphate (cAMP) (100 microM) as a pharmacological inducer of gap junctions. alpha-Glycyrrhetinic acid (25 microM), on the other hand, strongly inhibited both gap junction-mediated intercellular communication and the bystander effect, thus confirming the role of gap junctions in HSV-tk-mediated bystander killing. Using cytosine arabinoside as a growth inhibitor, we underlined the role of tumor cell proliferation in the sensitivity of HSV-tk-transfected cells to ganciclovir and demonstrated its correlation with the importance of the bystander effect.
Disciplines :
Surgery
Author, co-author :
Robe, Pierre ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Département des sciences biomédicales et précliniques
Princen, Frédéric
Martin, Didier ; Université de Liège - ULiège > Département des sciences cliniques > Neurochirurgie
Malgrange, Brigitte ; Université de Liège - ULiège > CNCM/ Centre fac. de rech. en neurobiologie cell. et moléc.
Stevenaert, Achille ; Université de Liège - ULiège > Services généraux (Faculté de médecine) > Relations académiques et scientifiques (Médecine)
Moonen, Gustave ; Université de Liège - ULiège > Département des sciences cliniques > Neurologie - Doyen de la Faculté de Médecine
Gielen, Jean-Louis ; Centre Hospitalier Universitaire de Liège - CHU > Chirurgie maxillo-faciale et plastique
Merville, Marie-Paule ; Université de Liège - ULiège > Département de pharmacie > Chimie médicale
Bours, Vincent ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Génétique générale et humaine
Language :
English
Title :
Pharmacological Modulation of the Bystander Effect in the Herpes Simplex Virus Thymidine Kinase/Ganciclovir Gene Therapy System: Effects of Dibutyryl Adenosine 3',5'-Cyclic Monophosphate, Alpha-Glycyrrhetinic Acid, and Cytosine Arabinoside
Culver K.W., Ram Z., Wallbridge S., Ishi H., Oldfield E.H., Blaese R.M. In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. Science. 256:1992;1550-1552.
Craperi D., Vicat J.-M., Nissou M.-F., Mathieu J., Baudier J., Benabid A.L., Verna J.-M. Increased Bax expression is associated with cell death induced by ganciclovir in a herpes thymidine kinase gene-expressing glioma cell line. Hum Gene Ther. 10:1999;679-688.
Rubsam L.Z., Davidson B.L., Shewach D.S. Superior cytotoxicity with ganciclovir compared with acyclovir and 1-β-D-arabinofuranosylthymine in herpes simplex virus-thymidine kinase-expressing cells A novel paradigm for cell killing . Cancer Res. 58:1998;3873-3882.
Halloran P.J., Fenton R.G. Irreversible G2-M arrest and cytoskeletal reorganization induced by cytotoxic nucleoside analogues. Cancer Res. 58:1998;3855-3865.
Ram Z., Culver K.W., Walbridge S., Blaese R.M., Oldfield E.H. In situ retroviral-mediated gene transfer for the treatment of brain tumor in rats. Cancer Res. 53:1993;83-88.
Colombo B.M., Benedetti S., Ottolenghi S., Mora M., Pollo B., Poli G., Finocchiaro G. The "bystander effect" Association of U-87 cell death with ganciclovir-mediated apoptosis of nearby cells and lack of effect in athymic mice . Hum Gene Ther. 6:1995;763-772.
Zlokovic B.V., Apuzzo M.L.J. Cellular and molecular neurosurgery Pathways from concept to realityPart 1: Target disorders and concept approaches to gene therapy of the central nervous system . Neurosurgery. 40:1997;789-803.
Bi W.L., Parysek L.M., Warnik R., Stambrook P.J. In vitro evidence that metabolic cooperation is responsible for the bystander effect observed with HSV-tk retroviral gene therapy. Hum Gene Ther. 4:1993;725-731.
Gagandeep S., Brew R., Green B., Christmas S.E., Klatzmann D., Poston G.J., Kinsella A.R. Prodrug-activated gene therapy Involvement of an immunological component in the bystander effect . Cancer Gene Ther. 3:1996;83-88.
Ram Z., Culver K.W., Walbridge S., Frank J.A., Blaese R.M., Oldfield E.H. Toxicity studies of retroviral-mediated gene transfer for the treatment of brain tumors. J Neurosurg. 79:1993;400-407.
Du L., Bai S., Whittle I.R., He L. Mechanisms underlying the bystander killing effect of experimental glioma cells in herpes simplex virus thymidine kinase/ganciclovir system. Cancer Gene Ther. 4:1997;305.
Paillard F. Bystander effects in enzyme/prodrug gene therapy. Hum Gene Ther. 8:1997;1733-1735.
Princen F., Robe P.A., Lechanteur C., Mesnil M., Rigo J.-M., Gielen J., Merville M.-P., Bours V. Cell type specific and gap junction mechanism for the HSV-tk/GCV mediated bystander effect. Clin Cancer Res. 5:1999;3639-3644.
Ishii-Morita H., Agbaria R., Mullen C.A., Hirano H., Koeplin D.A., Ram Z., Oldfield E.H., Johns D.G., Blaese R.M. Mechanism of `bystander effect' killing in the herpes simplex thymidine kinase gene therapy model of cancer treatment. Gene Ther. 4:1997;244-251.
Dilber M.S., Abedi M.R., Christensson B., Björkstrand B., Kidder G.M., Naus C.C.G., Gahrton G., Smith C.I. Gap junctions promote the bystander effect of herpes simplex thymidine kinase in vivo. Cancer Res. 57:1997;1523-1528.
Denning C., Pitts J.D. Bystander effects of different enzyme-prodrug systems for cancer gene therapy depend on different pathways for intercellular transfer of toxic metabolites, a factor that will govern clinical choice of appropriate regimes. Hum Gene Ther. 8:1997;1825-1835.
Goldberg G and Bertram JS, Correspondence re: Z. Ram et al., In situ retroviral-mediated gene transfer for the treatment of brain tumors in rats (Cancer Res 53: 83-88, 1993). Cancer Res 54: 3947-3948, 1994.
Goldberg G and Bertram JS, Correspondence re: Z. Ram et al., In situ retroviral-mediated gene transfer for the treatment of brain tumors in rats (Cancer Res 53: 83-88, 1993). Cancer Res 54: 3947-3948, 1994.
Trosko J.E., Madhukar B.V., Chang C.-C. Endogenous and exogenous modulation of gap junctional intercellular communication Toxicological and pharmacological implications . Life Sci. 53:1993;1-19.
Goodenough D.A. Connexins, connexons, and intercellular communication. Annu Rev Biochem. 65:1996;475-502.
Nagy J.I., Patel D., Ochalski P.A., Stelmack G.L. Connexin30 in rodent, cat and human brain Selective expression in gray matter astrocytes, co-localization with connexin43 at gap junctions and late developmental appearance . Neuroscience. 88:1999;447-468.
Samejima Y., Meeruelo D. `Bystander killing' induces apoptosis and is inhibited by forskolin. Gene Ther. 2:1995;50-58.
Touraine R.L., Ishii-Morita H., Ramsey W.J., Blaese R.M. The bystander effect in the HSV-tk/ganciclovir system and its relationship to gap junctional communication. Gene Ther. 5:1998;1705-1711.
Touraine R.L., Vahanian N., Ramsey W.J., Blaese R.M. Enhancement of the herpes simplex virus thymidine kinase/ganciclovir bystander effect and its antitumor efficacy in vivo by pharmacologic manipulation of gap junctions. Hum Gene Ther. 9:1998;2385-2391.
Alley M.C., Scuderio D.A., Monks A., Hursey M.L., Czerwinski M.J., Fine D.L., Abbott B.J., Mayo J.G., Shoemaker R.H., Boyd M.R. Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay. Cancer Res. 48:1988;589-601.
Stewart W.W. Functional connections between cells as revealed by dye-coupling with a highly fluorescent naphthalimide tracer. Cell. 14:1978;741-759.
Mehta P., Bertram J.S., Loewenstein W.R. The actions of retinoids on cellular growth correlate with their actions on gap junctional communication. J Cell Biol. 108:1989;1053-1065.
Hayashi T., Matesic D.F., Nomata K., Kang K.-S., Chang C.-C., Trosko J.E. Stimulation of cell proliferation and inhibition of gap junctional intercellular communication by linoleic acid. Cancer Lett. 112:1997;103-111.
Fryer H.J.L., Davis G.E., Manthorpe M., Varon S. Lowry protein assay using an automatic microtiter plate spectrophotometer. Anal Biochem. 153:1986;262-266.
Li W.E., Ochalski P.A., Hertzberg E.L., Nagy J.I. Immunorecognition, ultrastructure and phosphorylation status of astrocytic gap junctions and connexin43 in rat brain after cerebral focal ischaemia. Eur J Neurosci. 10:1998;2444-2463.
Naus C.C.G., Elisevich K., Zhu D., Belliveau D.J., Del Maestro R.F. In vivo growth of C6 glioma cells transfected with connexin43 cDNA. Cancer Res. 52:1992;4208-4213.
Zhu D., Kidder G.M., Caveney S., Naus C.C.G. Growth retardation in glioma cells cocultured with cells overexpressing a gap junction protein. Proc Natl Acad Sci USA. 89:1992;10218-10221.
Davidson J.S., Baumgarten I.M., Harley E.H. Reversible inhibition of intercellular junctional communication by glycyrrhetinic acid. Biochem Biophys Res Commun. 134:1986;29-36.
Davidson J.S., Baumgarten I.M. Glycyrrhetinic acid derivatives A novel class of inhibitors of gap-junctional intercellular communication. Structure-activity relationships . J Pharmacol Exp Ther. 246:1988;1104-1107.
Boviatsis E.J., Chase M., Wei M.X., Tamiya T., Hurford R.K. Jr, Kowall N.W., Tepper R.I., Breakefield X.O., Chiocca E.A. Gene transfer into experimental brain tumors mediated by adenovirus, herpes simplex virus, and retrovirus vectors. Hum Gene Ther. 5:1994;183-191.
Mesnil M., Piccoli C., Tiraby G., Willecke K., Yamasaki H. Bystander killing of cancer cells by herpes simplex virus thymidine kinase gene is mediated by connexins. Proc Natl Acad Sci USA. 93:1996;1831-1835.
Fick J., Barker F.G., Dazin P., Westphale E.M., Bayer E.C., Israel M.A. The extent of heterocellular communication mediated by gap junctions is predictive of bystander tumor cytotoxicity in vitro. Proc Natl Acad Sci USA. 92:1997;11071-11075.
Elshami A.A., Saavedra A., Zhang H., Kucharczuk J.C., Spray D.C., Fishman G.I., Amin K.M., Kaiser L.R., Albelda S.M. Gap junctions play a role in the `bystander effect' of the herpes virus thymidine kinase/ganciclovir system in vitro. Gene Ther. 3:1996;85-92.
Yamasaki H. Gap junctional intercellular communication and carcinogenesis. Carcinogenesis. 11:1990;1051-1058.
Bahn R.S., Zeller J.C., Smith T.J. n-Butyrate increases c-erb A oncogene expression in human colon fibroblasts . Biochem Biophys Res Commun. 150:1988;259-262.
Mitsuhashi T., Uchimura H., Takaku F. n-Butyrate increases the level of thyroid hormone nuclear receptor in non-pituitary cultured cells. J Biol Chem. 262:1987;3993-3999.
Vaziri C., Stice L., Faller D.V. Butyrate-induced G1 arrest results from p21-independent disruption of retinoblastoma protein-mediated signals. Cell Growth Differ. 9:1998;465-474.
Xue S., Rao P.N. Sodium butyrate blocks HeLa cells preferentially in early G1 phase of the cell cycle. J Cell Sci. 51:1981;163-171.
Bruce J.H., Ramirez A., Lin L., Agarwal R.P. Effects of cyclic AMP and butyrate on cell cycle, DNA, RNA, and purine synthesis of cultured astrocytes. Neurochem Res. 17:1992;315-320.
Feng P., Ge L., Akyhani N., Liau G. Sodium butyrate is a potent modulator of smooth muscle cell proliferation and gene expression. Cell Prolif. 29:1996;231-241.
Yu W., Dahl G., Werner R. The connexin 43 gene is responsive to oestrogen. Proc R Soc B Biol Sci. 255:1994;125-132.
Musil L.S., Cunningham B.A., Edelman G.M., Goodenough D.A. Differential phosphorylation of the gap junction protein connexin43 in junctional communication-competent and -deficient cell lines. J Cell Biol. 111:1990;2077-2088.
Stagg R.B., Fletcher W.H. The hormone-induced regulation of contact-dependent cell-cell communication by phosphorylation. Endocr Rev. 11:1990;302-325.
Azarnia R., Russel T.R. Cyclic AMP effects on cell-to-cell junctional membrane permeability during adipocyte differentiation of 3T3-L1 fibroblasts. J Cell Biol. 100:1985;265-269.