Adhesion of Human Glioma Cell Lines to Fibronectin, Laminin, Vitronectin and Collagen I Is Modulated by Gangliosides in vitro

References

• Albelda S. M., Buck C. A. Integrins and other cell adhesion molecules. FASEB. J. 1990; 4: 2868–2880
   PubMed Web of Science ®Google Scholar
• Burger P. C., Vogel F. S., Green S. B., Strike T. A. Glioblastoma multiforme and anaplastic astrocytoma: pathological criteria and prognostic implications. Cancer 1985; 56: 1106–1111
   PubMed Web of Science ®Google Scholar
• Cheresh D. A., Pierschbacher M. D., Herzig M. A., Mujoo K. Disialogangliosides GD2 and GD3 are involved in the attachment of human melanoma and neuroblastoma cells to extracellular matrix proteins. J. Cell Biol. 1986; 102: 688–696
   PubMed Web of Science ®Google Scholar
• Cheresh D. A., Pytela R., Pierschbacher M. D., Klier F. G., Ruoslahti E., Reisfeld R. A. An Arg-Gly-Asp-directed receptor on the surface of human melanoma cells exists in an divalent cation-dependent functional complex with the disialoganglioside GD2. J. Cell Biol. 1987; 105: 1163–1173
   PubMed Web of Science ®Google Scholar
• Curtis R., Cohen J., Fok-Seang J., Hanley M. R., Gregson N. A., Reynolds R., Wilkin G. P. Development of macroglial cells in rat cerebellum. I. Use of antibodies to follow early in vivo development and migration of oligodendrocytes. J. Neurocytol. 1988; 17: 43–54
   PubMedGoogle Scholar
• Fishman P. H., Brady R. O. Biosynthesis and function of gangliosides. Science 1976; 194: 906–915
   PubMed Web of Science ®Google Scholar
• Frame M. C., Freshney R. I., Vaughan P. F., Graham D. I., Shaw R. Interrelationship between differentiation and malignancy-associated properties in glioma. Brit. J. Cancer 1984; 49: 269–280
   PubMed Web of Science ®Google Scholar
• Fredman P., Magnani G. L., Nirenberg M., Ginsberg V. Monoclonal antibody A2B5 reacts with many gangliosides in neuronal tissue. Arch. Biochem. Biophys. 1984; 233: 661–666
   PubMed Web of Science ®Google Scholar
• Gladson C. L., Cheresh D. A. Glioblastoma expression of vitronectin and the alpha v beta 3 integrin. Adhesion mechanism for transformed glial cells. J. Clin. Invest. 1991; 88: 1924–1932
   PubMed Web of Science ®Google Scholar
• Hakomori S. I. Glycosphingolipids in cellular interaction, differentiation and oncogenesis. Ann. Rev. Biochem. 1981; 50: 733–764
   PubMed Web of Science ®Google Scholar
• Hakomori S. I. Bifunctional role of glycosphigolipids. J. Biol. Chem. 1990; 265: 18713–18716
   PubMed Web of Science ®Google Scholar
• Hynes R. O. Integrins: versatility, modulation, and signalling in cell adhesion. Cell 1992; 69: 11–25
   PubMed Web of Science ®Google Scholar
• Kakita A., Wakabayashi K., Takahashi H., Ohama E., Ikuta F., Tbkiguchi S. Primary leptomeningeal glioma: Ultrastructural and laminin immunohistochemical studies. Acta Neuropathol. 1992; 83: 538–542
   PubMed Web of Science ®Google Scholar
• Kepes J. J., Rubinstein L. J., Eng L. F. Peomorphic xaonthoastrocytoma: a distinctive meningocerebral glioma of young subjects with relatively favorable prognosis. A study of 12 cases. Cancer 1979; 44: 1839–1852
   PubMed Web of Science ®Google Scholar
• Kleinman H. K., McGarvey M. L., Hassell J. R., Star V. L., Cannon F. B., Laurie G. W., Martin G. R. Basement membrane complexes with biological activity. Biochemistry 1986; 25: 312–318
   PubMed Web of Science ®Google Scholar
• Knott J. C. A., Edwards A. J., Gullan R. W., Clarke T. M., Pilkington G. J. A human glioma cell line retaining expression of GFAP and gangliosides, recognized by A2B5 and LB1 antibodies, after prolonged passage. Neuropath. Appl. Neu-robiol. 1990; 16: 489–500
   PubMed Web of Science ®Google Scholar
• Koochekpour S., Merzak A., Pilkington G. J. Control of glioma cell proliferation, morphology and migration by basement membrane in vitro. Eur. J. Cancer 1994, In press
   Google Scholar
• Kundu S., Pleetman M., Redwine W., Boyd A., Marcus D. Binding of monoclonal antibody A2B5 to gangliosides. Biochem. Biophys. Res. Commun. 1983; 116: 836–842
   PubMed Web of Science ®Google Scholar
• Kung P. C., Lee J. C., Bakay L. Vascular invasion by glioma cells in man: an electron microscopy study. J. Neuro-surg. 1969; 31: 339–345
   Google Scholar
• McComb R. D., Bigner D. D. Immunolocalization of Iaminin in neoplasms of the central and peripheral nervous systems. J. Neuropath. Exp. Neurol. 1985; 44: 242–253
   PubMed Web of Science ®Google Scholar
• McKeever P. E., Fligiel S. E. G., Varani J., Castle R. L., Hood T. W. Products of cells cultured from gliomas. VII. Extracellular matrix proteins of gliomas which contain glial fibrillary acidic protein. Lab. Invest. 1989; 60: 286–295
   PubMed Web of Science ®Google Scholar
• Merzak A., Koochekpour S., Pilkington G. J. Cell surface gangliosides are involved in the control of human glioma cell invasion in vitro. Neurosci. Letters 1994a; 177: 44–46
   PubMed Web of Science ®Google Scholar
• Merzak A., Koochekpour S., Pilkington G. J. CD44 mediates human glioma cell adhesion and invasion in vitro. Cancer Res. 1994b; 54: 3988–3992
   PubMed Web of Science ®Google Scholar
• Merzak A., Parker C., Koochekpour C., Sherbet G., Pilkington G. J. Overexpression of the 18A2/mts1 gene and down regulation of the TIMP-2 gene in invasive human glioma cell lines in vitro. Neuropath. Appl. Neurobiol. 1994c; 20, In press
   PubMed Web of Science ®Google Scholar
• Merzak A., McCrea S., Koochekpour S., Pilkington G. J. Control of human glioma cell growth, migration, and invasion in vitro by transforming growth factor-betal. Br. J. Cancer 1994d; 70: 199–203
   PubMed Web of Science ®Google Scholar
• Merzak A., Koochekpour S., McCrea S., Roxanis Y., Pilkington G. J. Gangliosides modulate proliferation, migration and invasiveness of human brain tumour cells in vitro. Molecular and Chemical Neuropathology 1994, In press
   Google Scholar
• Morris C. S., Esiri M. M. Immunocytochemical study of macrophages and microglial cells and extracellular matrix components in human CNS disease. 1: Gliomas. J. Neurol. Sci. 1991; 101: 47–58
   PubMed Web of Science ®Google Scholar
• Mugnai G., Lewandowska K., Choi H. U., Rosenberg L. C., Culp L. A. Ganglioside-dependent adhesion events of human neuroblastoma cells regulated by the RGDS-dependent fibronectin receptor and proteoglycans. Exp. Cell Res. 1988; 175: 229–247
   PubMed Web of Science ®Google Scholar
• Paulus W., Roggendorf W., Schuppan D. Immunohistochemical investigation of collagen subtypes in human glioblastomas. Virchows Arch. Pathol. Anal. 1988; 413: 325–332
   Web of Science ®Google Scholar
• Paulus W., Schloe W., Perentes E., Jacobi G., Warmuth-Metz M., Roggendorf W. Desmoplastic supratentorial neuroepithelial tumors of infancy. Histopathology 1992; 21: 43–49
   PubMed Web of Science ®Google Scholar
• Paulus W., Baur I., Schuppan D., Roggendorf W. Characterization of integrin receptors in normal and neoplastic human brain. Am. J. Pathol. 1993; 143: 154–163
   PubMed Web of Science ®Google Scholar
• Paulus W., Tonn J. C. Basement membrane invasion of glioma cells mediated by integrin receptors. J. Neurosurg. 1994; 80: 515–519
   PubMed Web of Science ®Google Scholar
• Peters A., Palay S. L., de Webster H. F. The fine structure of the nervous system: Neurons and their supporting cells, Ed 3. Oxford University Press, New York 1991
   Google Scholar
• Pilkington G. J. Glioma heterogeneity in vitro: the significance of growth factors and gangliosides. Neuropath. Appl. Neurobiol. 1992; 18: 434–442
   PubMed Web of Science ®Google Scholar
• Prater C. A., Plotkin J., Jaye D., Frazier W. A. The properdin-like type I repeats of human thrombospondin contain a cell attachment site. J. Cell Biol. 1991; 112: 1031–1040
   PubMed Web of Science ®Google Scholar
• Russell D. S., Rubinstein L. J. Pathology of Tumours of the Nervous System, Ed. 5. Williams & Wilkens, Baltimore, MD 1989; 83–289
   Google Scholar
• Rutka J. T., Apodaca G., Stern R., Rosenblum M. The extracellular matrix of the central and peripheral nervous systems: structure and function. J. Neurosurg. 1988; 69: 155–170
   PubMed Web of Science ®Google Scholar
• Salcman M. Survival in glioblastoma: historical perspective. Neurosurgery 1980; 7: 435–439
   PubMed Web of Science ®Google Scholar
• Small R. K., Riddle P., Noble M. Evidence for migration of oligodendrocyte-type 2 astrocyte progenitor cells into developing rat optic nerve. Nature 1987; 328: 155–157
   PubMed Web of Science ®Google Scholar
• Stallcup W. B. Involvement of gangliosides and glycoprotein fibronectin receptors in cellular adhesion to fibronectin. Exp. Cell Res. 1988; 177: 90–102
   PubMed Web of Science ®Google Scholar
• Thompson L. K., Horowitz P. M., Bentley K. L., Thomas D. D., Alderete J. F., Klebe R. J. Localization of the ganglioside-binding site of fibronectin. J. Biol. Chem. 1986; 261: 5209–5214
   PubMed Web of Science ®Google Scholar
• Traylor T. D., Hogan E. L. Gangliosides of human cerebral astrocytomas. J. Neurochem. 1980; 34: 126–131
   PubMed Web of Science ®Google Scholar
• Venstrom K. A., Reichardt L. F. Extracellular matrix 2: role of extracellular matrix molecules and their receptors in the nervous system. FASEB. J. 1993; 7: 996–1003
   PubMed Web of Science ®Google Scholar
• Ziche M., Morbidelli L., Alessandri J., Gullino P. M. Angiogenesis can be stimulated or repressed in vivo by a change in GM3:GD3 ganglioside ratio. Lab. Invest. 1992; 67: 711–715
   PubMed Web of Science ®Google Scholar