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1998 | 45 | 2 |

Tytuł artykułu

Comparative study of sialidase activity and Gm3 content in B16 melanoma variants with different metastatic potential

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
We previously demonstrated that transfection of a sialidase cDNA into B16-BL6 cells, a highly metastatic and invasive cell line derived from the mouse B16 melanoma, resulted in a marked suppression of metastasis accompanied by decreased cellular content of the GM3 that is one of the target molecules of the sialidase expressed (Tokuyama et al., 1997 Int. J. Cancer, 73, 410-415). To obtain further insight into the involvement of sialidase in metastasis, we made a comparison of the levels of sialidase activity and GM3 content between B16 melanoma cell lines with low (B16-F1) and high (B16-F10 and -BL6) metastatic potential. The cells exhibited sialidase activity towards 4-methylumbelliferyl N-acetylneuraminic acid (4MU-Neu5Ac) and gangliosides at acidic pH in the particulate fractions, but not in the cytosol. The activity toward 4MU-NeuAc was significantly lower in highly metastatic cells. The activity toward gangliosides, on the other hand, varied independently of metastatic potential: B16-F10 cells with a high potential for experimental metastasis showed the lowest level and B16-BL6 cells having high invasiveness had rather a higher level of ganglioside sialidase along with a much greater GM3 synthase activity than the other two cell lines. Flow cytometric analysis with anti-GM3 antibody revealed that highly metastatic cell lines were higher in the binding affinity as compared to B16-F1 cells, B16-BL6 cells containing twice as much cellular GM3 as B16-F1 cells on thin-layer chromatography.

Wydawca

-

Rocznik

Tom

45

Numer

2

Opis fizyczny

p.343-349,fig.

Twórcy

autor
  • Miyagi Prefectural Cancer Center, Medeshima-Shiode, Natori-shi, Miyagi 981-1293, Japan
autor
autor
autor
autor

Bibliografia

  • 1. Yogeeswaran, G. & Salk, P. (1981) Metastatic potential is positively correlated with cell sur­face sialylation of cultured murine tumor cell lines. Science 212, 1514-1516.
  • 2. Tao, T.-W. & Burger, M.M. (1982) Lectin- resistant variants of mouse melanoma cells. I. Altered metastasizing capacity and tumori- genicity. Int J. Cancer 29, 425-430.
  • 3. Fogel, M., Altevogt, P. & Schirrmacher, V. (1983) Metastatic potential severely altered by changes in tumor cell adhesiveness and cell- surface sialylation. J. Exp. Med. 157, 371- 376.
  • 4. Collard, J.G., Schijven, J.F, Bikker, A., La Riviere, G., Bolscher, J.G.M. & Roos, E. (1986) Cell surface sialic acid and the invasive and metastatic potential of T-eell hybridomas. Can­cer Res. 46, 3521-3527.
  • 2. 5. Passaniti, A. & Hart, G.W. (1988) Cell surface sialylation and tumor metastasis. Metastatic potential of B16 melanoma variants corre­lated with their relative numbers of specific penultimate oligosaccharide structures. J. Biol. Chem. 263, 7591-7603.
  • 6. Miyagi, T. & Tsuiki, S. (1984) RaUiver lysoso­mal sialidase. Solubilization, substrate speci­ficity and comparison with the cytosolic siali­dase. Eur. J. Biochem. 141, 75-81.
  • 7. Miyagi. T. & Tsuiki, S. (1985) Purification and characterization of cytosolic sialidase from rat liver. J. Biol Chem. 260. 6710-6716.
  • 8. Miyagi, T., Sagawa, J., Konno, K., Handa, S. & Tsuiki, S. (1990) Biochemical and immuno­logical studies on two distinct ganglioside- hydrolyzing sialidases from the particulate fraction of rat brain. J. Biochem. 107, 787-793.
  • 9. Miyagi, T., Sato, K.. Hata, K. & Taniguchi, S. (1994) Metastatic potential of transformed rat 3Y1 cell lines is inversely correlated with lysosomal type sialidase activity. FEBS Lett. 349, 255-259.
  • 10. Tokuyama, S., Moriya, S., Yasui, A., Miyazaki, J., Taniguchi, S. & Miyagi, T. (1997) Suprcs- sion of pulmonary metastasis in mouse B16 melanoma cells. Int J. Cancer 73,410-415.
  • 11. Miyagi, T., Koseki, M. & Tsuiki, S. (1988) Com­parative study of the levels of sialyltransfe- rases responsible for the formation of sugar chains in glycoproteins and gangliosides in ray liver and hepatomas. Jpn. J. Cancer Res. 79, 742-749.
  • 12. Poste, G., Doll, J., Hart, I.R. & Fidler, I.J. (1980) In vitro selection of murine B16 mela­noma variants with enhanced tissue invasive properties. Cancer Res. 40, 1636-1644.
  • 13. Fidler, IJ. (1973) Selection of successive tu­mor lines for metastasis. Nature New Biol. 242,148-149.
  • 14. Hara, S., Yamaguchi, M., Takemori, Y. & Nakamura, M. (1986) Highly sensitive deter­mination of 7V-acetyl- and N-glycolylneura- minic acids in human serum and urine and rat serum by reversed-phase liquid chromatogra­phy with fluorescence detection. J. Chroma- togr. 377, 111-119.
  • 15. Lieser, M., Harms. E., Kern, H., Bach, G. & Cantz, M. (1989) Ganglioside G^a sialidase ac­tivity in fibroblasts of normal individuals and of patients with sialidosis and mucolipidosis IV. Biochem. J. 260, 69-74.
  • 16. Kopitz, J., von Reitzenstein, C., Sinz, K. & Cantz, M. (1996) Selective ganglioside desialy- lation in the plasma membrane of human neu­roblastoma cells. Glycobiology 6. 367-376.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-5d72a22f-93e4-46eb-80d8-2ad8990ba5bc
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