Skip to main content
Log in

Effects of retionoids on invasion of organ cultures of chick chorioallantoic membrane by adenovirus transformed cells

  • Published:
In Vitro Cellular & Developmental Biology Aims and scope Submit manuscript

Summary

Invasion of chick chorioallantoic membrane (CAM) organ cultures by rat 3Y1 cells transformed by the highly oncogenic human adenovirus type 12 (3Y1/12-10 cells) was inhibited by several retinoids tested. The anti-invasive activity of the retinoids was dependent on retinoid concentration and continuous (4d) exposure of the CAM. The 50% retinoid dose (dose effective in achieving a response in half of the organ cultures) that inhibited invasion was 0.85 μg/ml of retinol palmitate, 0.39 μg/ml of retinoic acid, or 0.16 μg/ml of retinol acetate. This dose was of the same order of magnitude as that which induced CAM differentiation, and was three-to fourfold less than the dose that caused cytotoxic damage of CAM. In addition, the retinoids inhibited 3Y1/12-10 cell growth by approximately 40% at levels over 10-fold higher than those needed for anti-invasion activity. The findings suggest that the anti-invasive activity of retinoids was at least partly due to direct induction of cell differentiation of the CAM host tissue.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Armstrong, P. B.; Quigley, J. P.; Sidebottom, E. Transepithelial invasion and intramesenchymal infiltration of the chick embryo chorioallantois by tumor cell lines. Cancer Res. 42: 1826–1837; 1982.

    PubMed  CAS  Google Scholar 

  2. Bertram, J. S.; Mordan, L. J.; Domanska-Janik, K.; et al. Inhibition of in vitro neoplastic transformation by retinoids. In: Arnott, M. S.; van Eys, J.; Wang, Y. M., eds. Molecular interrelations of nutrition and cancer. New York: Raven Press; 1982:315–335.

    Google Scholar 

  3. Bollag, W. Retinoids and cancer. Cancer Chemother. Pharmacol. 3:207–215; 1979.

    Article  PubMed  CAS  Google Scholar 

  4. Borek, C. Vitamins and micronutrients modify carcinogenesis and tumor promotion in vitro. In: Arnott, M. S.; van Eys, J.; Wang, Y. M., eds. Molecular interrelations of nutrition and cancer. New York: Raven Press; 1982:337–350.

    Google Scholar 

  5. Donahoe, J.; Noyes, I.; Milo, G. E.; et al. A comparison of expression of neoplastic potential of carcinogen-transformed human fibroblasts in nude mice and in chick embryonic skin. In Vitro 18:429–434; 1982.

    PubMed  CAS  Google Scholar 

  6. Easty, D. M.; Easty, G. C. Measurement of the ability of cells to infiltrate normal tissues in vitro. Br. J. Cancer 29:36–49; 1974.

    PubMed  CAS  Google Scholar 

  7. Hart, I. R.; Fidler, I. J. An in vitro quantitative assay for tumor cell invasion. Cancer Res. 38:3218–3224; 1978.

    PubMed  CAS  Google Scholar 

  8. Jetten, A. M. Retinoids specifically enhance the number of epidermal growth factor receptors. Nature 284:626–629; 1980.

    Article  PubMed  CAS  Google Scholar 

  9. Ledinko, N.; Schaeufele, J.; Soorma, O. Adenovirus type 12 gene 401 function and maintenance of transformation. J. Virol. 29:250–260; 1979.

    PubMed  CAS  Google Scholar 

  10. Lotan, R. Effects of vitamin A and its analogs (retinoids) on normal and neoplastic cells. Biochim. Biophys. Acta 605:33–91; 1980.

    PubMed  CAS  Google Scholar 

  11. Lotan, R.; Lotan, D.; Kadouri, A. Comparison of retinoic acid effects on anchorage-dependent growth, anchorage-independent growth and fibrinolytic activity of neoplastic cells. Exp. Cell Res. 141:79–86; 1982.

    Article  PubMed  CAS  Google Scholar 

  12. Lotan, R.; Nicolson, G. L. Inhibitory effects of retinoic acid or retinyl acetate on the growth of untransformed, transformed, and tumor cells in vitro. J. Natl. Cancer Inst. 59:1717–1722; 1977.

    PubMed  CAS  Google Scholar 

  13. Lotan, R.; Thein, R.; Lotan, D. Suppression of the transformed cell phenotype expression by retinoids. In: Meyskens, F. L.; Prasad, K., eds. The modulation and mediation of cancer by retinoids. Basel: S. Karger AG; 1983:211–222.

    Google Scholar 

  14. Mayer, H.; Bollag, W.; Hänni, R.; et al. Retinoids, a new class of compounds with prophylactic and therapeutic activities in oncology and dermatology. Experienta 34:1105–1119; 1978.

    Article  CAS  Google Scholar 

  15. Milo, G. E.; Trewyn, R. W. In vitro transformation of cultured human diploid fibroblasts. In: Magee, P. N., ed. Banbury Report. Nitrosamines and human cancer, vol. 12, Cold Spring Harbor Laboratory; 1982:3–13.

  16. Noguchi, P. D.; Johnson, J. B.; O’Donnell, R.; et al. Chick embryonic skin as a rapid organ culture assay for cellular neoplasia. Science 199:980–983; 1978.

    Article  PubMed  CAS  Google Scholar 

  17. Ossowski, L.; Reich, E. Experimental model for quantitative study of metastasis. Cancer Res. 40:2300–2309; 1980.

    PubMed  CAS  Google Scholar 

  18. Poste, G.; Doll, J.; Hart, I. R.; et al. In vitro selection of murine B16 melanoma variants with enhanced tissue-invasive properties. Cancer Res. 40:1636–1644; 1980.

    PubMed  CAS  Google Scholar 

  19. Poste, G.; Flood, M. K. Cells transformed by temperature-sensitive mutants of avian sarcoma virus cause tumors in vivo at permissive and nonpermissive temperatures. Cell 17:789–800; 1979.

    Article  PubMed  CAS  Google Scholar 

  20. Scher, C. D.; Haudenschild, C.; Klagsbrun, M. The chick chorioallantoic membrane as a model system for the study of tissue invasion by viral transformed cells. Cell 8:373–382; 1976.

    Article  PubMed  CAS  Google Scholar 

  21. Sporn, M. B. Retinoids and carcinogenesis. Nutr. Rev. 35:65–69; 1977.

    Article  PubMed  CAS  Google Scholar 

  22. Sporn, M. B.; Newton, D. L. Retinoids and chemoprevention of cancer. In: Zedeck, M. S.; Lipkin, M., eds. Inhibition of tumor induction and development. New York: Plenum Publishing Corp.; 1981:71–100.

    Google Scholar 

  23. Sporn, M. B.; Roberts, A. B. Role of retinoids in differentiation and carcinogenesis. Cancer Res. 43:3034–3040; 1983.

    PubMed  CAS  Google Scholar 

  24. Strickland, S.; Mahdavi, V. The induction of differentiation in teratocarcinoma stem cells by retinoic acid. Cell 15:393–403; 1978.

    Article  PubMed  CAS  Google Scholar 

  25. Strickland, S.; Smith, K. K.; Marotti, K. R. Hormonal induction of differentiation in teratocarcinoma stem cells: generation of parietal endoderm by retinoic acid and dibutyryl cAMP. Cell 21:347–355; 1980.

    Article  PubMed  CAS  Google Scholar 

  26. Weber, W. T.; Mausner, R. Migration patterns of avian embryonic bone marrow cells and their differentiation to functional T and B cells. In: Benedict, A. A., ed. Avian immunology. New York: Plenum Publishing Co.; 1977;47–59.

    Google Scholar 

  27. Westin, E. H.; Wong-Stall, F.; Gelmann, E. P.; et al. Expression of cellular homologues of retroviral onc genes in human hematopoietic cells. Proc. Natl. Acad. Sci. USA 79:2490–2494; 1982.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This work was supported by National Cancer Institute Grant CA 13231 and by University of Akron Grant RG 832.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fazely, F., Moses, D.C. & Ledinko, N. Effects of retionoids on invasion of organ cultures of chick chorioallantoic membrane by adenovirus transformed cells. In Vitro Cell Dev Biol 21, 409–414 (1985). https://doi.org/10.1007/BF02623472

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02623472

Key words

Navigation