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Characterization of Newly Established Cells Which Provide an Animal Model for Spontaneous Metastasis

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Part of the book series: Animal Cell Technology: Basic & Applied Aspects ((ANICELLTECH,volume 5))

Abstract

A novel cell line, r/mHM-SFME-1 (r/mHM-1) was established from ras/myc SFME cells transformed by human c-Ha-ras and mouse c-myc genes (SFME cells have been established from a Balb/c mouse embryo in a serum-free culture condition). This cell line was derived from a pulmonary metastasis developed in a Balb/c mouse which had been transplanted subcutaneously with pSV2-neo introduced ras/myc SFME cells. The r/mHM-1 cells had an ability to spontaneously metastasize into the lungs of syngeneic mice when injected subcutaneously, and survival of the mice which received the r/mHM-1 cells was significantly shorter than ones with ras/myc SFME cells. The r/mHM-1 cells grew slowly in vitro than their parental ras/myc SFME ones did, and produced dispersed colonies in agar whereas their parental ones produced packed ones. A urokinase type plasminogen activator activity was detected in the culture fluid in which the r/mHM-1 cells were cultured for 2 days, whereas the activity was not detected in those from the parent ones.

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References

  1. Shih, C. and Weinberg, R. A. ‘Isolation of a transforming sequence from a human bladder carcinoma cell line’, Cell, 29, 161–169, (1982).

    Article  PubMed  CAS  Google Scholar 

  2. Sakamoto, H., Mori, M., Taira, M., Yoshida, T., Matsukawa, S., Shimizu, K., Sekiguchi, M., Terada, M. and Sugimura, T. ‘Transforming gene from human stomach cancers and a noncancerous portion of stomach mucosa’, Proc. Natl. Acad. Sci. USA, 83, 3997–4001, (1986).

    Article  PubMed  CAS  Google Scholar 

  3. Loo, D. T., Fuquay, J. I., Rawson, C. L. and Barnes, D. W. ‘Extended culture of mouse embryo cells without senescence: Inhibition by serum’, Science, 236, 200–202 (1987).

    Article  PubMed  CAS  Google Scholar 

  4. Rawson, C. L., Shirahata, S., Collodi, P., Natsuno, T. and Barnes, D. W. ‘Oncogene transformation frequency of nonsenescent SFME cells is increased by c-myc’, Oncogene, 6, 487–489 (1991).

    PubMed  CAS  Google Scholar 

  5. Shirahata, S., Rawson, C. L., Loo, D. T., Chang, Y. J. and Barnes, D. W. ‘Ras and neu oncogenes reverse serum inhibition and epidermal growth factor dependence of serum-free mouse embryo cells’, J. Celluar Physiol., 144, 69–76, (1990).

    Article  CAS  Google Scholar 

  6. Loo, D. T., Rawson, C. L., Helmrich, A. and Barnes, D. W. ‘Serum-free mouse embryo cells: Growth response in vitro’, J. Cellular Physiol., 139, 484–491, (1989).

    Article  CAS  Google Scholar 

  7. Carmichael, J., Degraff, W. G., Gazdar, A. F., Minna, J. D. and Mitchell, J. B. ‘Evaluation of a tetrazolium-based semiautomated colorimetric assay: Assessment of chemosensitivity testing’, Cancer Research., 47, 936–942 (1987).

    PubMed  CAS  Google Scholar 

  8. Sambrook, J., Fritsh, E. F. and Maniatis, T. “Molecular cloning, A laboratory manual” Second Edition. pp. 7.26–7.52 (1989) Cold Spring Harbor Laboratory Press, New York.

    Google Scholar 

  9. Capon, D. J., Chen, E. Y., Levinson, A. D., Seeburg, P. H. and Goeddel, D. V. ‘Complete nucleotide sequences of the T24 human bladder carcinoma oncogene and its normal homologue’, Nature, 302, 33–37 (1983).

    Article  PubMed  CAS  Google Scholar 

  10. Feinberg, A. P. and Vogelstein, B. ‘Addendum of “A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity”’, Analytical Biochem., 137, 266–267 (1984).

    Article  CAS  Google Scholar 

  11. Chomczynski, P. and Sacchi, N. ‘Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction’, Analytical Biochem., 162, 156–159 (1987).

    Article  CAS  Google Scholar 

  12. Saksela, O. ‘Radial caseinolysis in agarose: A simple method for detection of plasminogen activator in the presence of inhibitory substances and serum’, Analyt. Biochem., 111, 276–282, (1981).

    Article  PubMed  CAS  Google Scholar 

  13. Ichikawa, T., Kyprianou N. and Isaacs, J. T. ‘Genetic instability and the acquisition of metastatic ability by rat mammary cancer cells following v-H-ras oncogene transfection’, Cancer Res., 50, 6349–6357, (1990).

    PubMed  CAS  Google Scholar 

  14. Yoshikura, H. ‘ Suppression of focus formation by bovine papillomavirus-transformed cells by contact with non-transformed cells: Involvement of sugar(s) and phosphorylation’, Inter. J. Cancer, 44, 885–891, (1989).

    Article  CAS  Google Scholar 

  15. Naito, A., Kitamura, Y., Sudoh, K. and Yoshikura, H. ‘In vitro “progression” of bovine papillomavirus-transformed cells: Loss of contact sensitivity after multiple rounds of selection’, Inter. J. Cancer, 48, 889–894, (1991).

    Article  CAS  Google Scholar 

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© 1993 Springer Science+Business Media Dordrecht

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Nomura, T. et al. (1993). Characterization of Newly Established Cells Which Provide an Animal Model for Spontaneous Metastasis. In: Kaminogawa, S., Ametani, A., Hachimura, S. (eds) Animal Cell Technology: Basic & Applied Aspects. Animal Cell Technology: Basic & Applied Aspects, vol 5. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-2044-9_3

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  • DOI: https://doi.org/10.1007/978-94-011-2044-9_3

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-4905-4

  • Online ISBN: 978-94-011-2044-9

  • eBook Packages: Springer Book Archive

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