Abstract
The human glioma cell line, NP-1, expresses IL-8 mRNA and constitutively secretes IL-8 protein. Administration of recombinant IL-8 increased the proliferation of NP-1 cells in a dose-dependent manner. In the presence of anti-IL-8 antiserum, the IL-8 mediated proliferation of NP-1 cell growth was inhibited. Further, NP-1 cell growth was inhibited by transfection of retroviral constructs encoding antisense IL-8 bothin vitro andin vivo models. These results suggest that antisense IL-8 gene therapy could be beneficial in gliomas where autocrine stimulation by IL-8 is implicated.
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References
Fontana A, Hengartner H, de Tribolet N, Weber E: Glioblastoma cells release interleukine 1 and factors inhibiting interleukin 2-mediated effects. J Immunol 132: 1837–1844, 1984
Lichter T, Dohrmann GJ, Gurney ME: Cytokine gene expression by human gliomas. Neurosurgery 26: 788–793, 1990
Nishida T, Nakai S, Kawakami T, Aihara K, Nishino N, Hirai Y: Dexamethasone regulation of the expression of cytokine mRNAs induced by interleukin-1 in the astrocytoma cell line U373MG. FEBS Lett 243: 25–29, 1989
Yasukawa K, Hirano T, Watanabe Y, Muratani K, Matsuda T, Nakai S, Kishimoto T: Structure and expression of human B cell stimulatory factor-2 (BSF-2/IL-6). EMBO J 6: 2939–2945, 1987
Bethea JR, Gillespie GY, Chung IY, Benveniste EN: Tumor necrosis factor production and receptor expression by a human malignant glioma cell line, D54-MG. J Neuroimmunol 30: 1–13, 1990
Carrell S, de Tribolet N, Gross N: Expression of HLA-DR and common acute lymphoblastic leukemia antigens on glioma cells. Eur J Immunol 12: 354–357, 1982
Takiguchi M, Ting JPY, Buessow SC, Boyer C, Gillespie Y, Frelinger JA: Response of glioma cells to γ-interferon. Eur J Immunol 15: 809–814, 1985
Yamazaki K: Tumorigenicity of established human glioma cell lines in lasat and nude mice. Shinkeibyourigaku 3: 29–38, 1982
Chirgwin JM, Przybyla AE, MacDonald RJ, Rutter WJ: Isolation of biologically active ribunucleic acid from sources enriched in ribonuclease. Biochemistry 18: 5294–5299, 1979
Thomas PS: Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci USA 77: 5201–5205, 1980
Barna BP, Estes ML, Jacobs B, Hudson S, Ransohoff RM: Human astrocytes proliferate in response to tumor necrosis factor alpha. J Neuroimmunol 30: 239–243, 1990
Korman AJ, Frantz JD, Strominger JL, Mulligan RC: Expression of human class II major histocompatibility complex antigens using retrovirus vectors. Proc Natl Acad Sci USA 84: 2150–2154, 1987
Price J, Turner D, Cepko C: Lineage analysis in the vertebrate nervous system by retrovirus mediated gene transfer. Proc Natl Acad Sci USA 84: 156–160, 1987
Mann R, Mulligan RC, Baltimore D: Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus. Cell 33: 153–159, 1983
Sambrook J, Fritsch EF, Maniatis T: Molecular cloning: A laboratory manual, ed 2, Cold Spring Harbor, NY: Cold Spring Harbor Laboratories, 1989
Yoshirnura T, Matsushima K, Oppenheim J, Leonard E: Neutrophil chemotactic factor produced by lipopolysaccharide (LPA)-stimulated human mononuclear leukocytes: partial characterization and separation from interleukin 1 (IL-1). J Immunol 139: 788–793, 1987
Larsen CG, Anderson AO, Appella E, Oppenheim J, Matsushima K: The neutrophil-activating protein (NAP-1) is also chemotactic for T lymphocytes. Science 243: 1464–1466, 1989
Schroder JM, Mrowietz U, Morta E, Christophers E: Purification and partial biochemical characterization of a human monocyte-derived, neutrophil-activating peptide that lacks interleukin 1 activity. J Immunol 139: 3474–3483, 1987
Peveri P, Walz A, Dewald B, Baggiolini M: A novel neutrophil activating factor produced by human mononuclear phagocytes. J Exp Med 167: 1547–1559, 1988
Van Damme J, Beeumen J, Opdenakker G, Billiau A: A novel, NH2-terminal sequence characterized human monokine possessing neutrophil chemotactic, skin reactive and granulocytosis-promoting activity. J Exp Med 167: 1364–1376, 1988
Frei K, Bodmer S, Schwerde C, Fontana A: Astrocytes of the brain synthesize interleukin-3 like factors. J Immunol 135: 4044–1047, 1985
Larsson I, Landstrom LE, Larnor E, Lundgren E, Miorner H, Strannegard O: Interferon production in glia and glioma cell lines. Infect Immun 22: 786–789, 1978
Bodmer S, Siepl C, Fontana A: Immunoregulatory factors secreted by glioblastoma cells: glioblastoma derived T-cell suppressor factor/transforming growth factor-β2. In: Goetzl EJ, Spector NH (eds) Neuroimmune Networks: Physiology and Diseases. Alan R. Liss Inc, New York, 73–82, 1989
Yamanaka R, Tanaka R, Saitoh T: Cytokine gene expression on the glioma cells and specimens. J Neuro-oncology 21: 243–247, 1994
Culver KW, Ram Z, Wallbridge S, Ishii H, Oldfield EH, Blaese RM:In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. Science 256: 1550–1552, 1992
Huber BE, Richans CA, Krenitsky TA: Retroviral-mediated gene therapy for the treatment of hepatocellular carcinoma: an innovative approach for cancer therapy. Proc Natl Acad Sci USA 88: 8039–8043, 1991
Moolten FL, Wells JM: Curability of tumors bearing herpes thymidine kinase genes transferred by retroviral vectors. J Natl Cancer Inst 82: 297–300, 1990
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Yamanaka, R., Tanaka, R., Yoshida, S. et al. Growth inhibition of human glioma cells modulated by retrovirus gene transfection with antisense IL-8. J Neuro-Oncol 25, 59–65 (1995). https://doi.org/10.1007/BF01054723
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DOI: https://doi.org/10.1007/BF01054723