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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1981 Jun;78(6):3834–3838. doi: 10.1073/pnas.78.6.3834

Immunochemical delineation of an oncofetal antigen on normal and simian virus 40-transformed human fetal melanocytes.

A C Morgan Jr, D R Galloway, F C Jensen, B C Giovanella, R A Reisfeld
PMCID: PMC319667  PMID: 6267607

Abstract

Human melanoma cells of uveal origin shed 94,000- and 240,000-dalton glycoproteins in common with most melanoma cell lines of dermal origin. Normal human melanocytes derived from fetal uvea shed a 90,000-dalton glycoprotein that was found to be immunologically identical with the 94,000-dalton glycoprotein of melanoma cells. Expression of this 90,000-dalton molecule was confined to fetal cells of ectodermal origin. After simian virus 40 (SV40) transformation of human fetal melanocytes, there was an apparent increase in molecular size of this component to 94,000 daltons. In contrast, the 240,000-dalton glycoprotein was not synthesized or shed by uninfected or SV40-transformed fetal melanocytes. These data suggest that the 94,000-dalton glycoprotein is an oncofetal antigen of ectodermal origin.

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Selected References

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  1. Berenblum I. Established principles and unresolved problems in carcinogenesis. J Natl Cancer Inst. 1978 Apr;60(4):723–726. doi: 10.1093/jnci/60.4.723. [DOI] [PubMed] [Google Scholar]
  2. Bissell M. J., Hatié C., Calvin M. Is the product of the src gene a promoter? Proc Natl Acad Sci U S A. 1979 Jan;76(1):348–352. doi: 10.1073/pnas.76.1.348. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bonner W. M., Laskey R. A. A film detection method for tritium-labelled proteins and nucleic acids in polyacrylamide gels. Eur J Biochem. 1974 Jul 1;46(1):83–88. doi: 10.1111/j.1432-1033.1974.tb03599.x. [DOI] [PubMed] [Google Scholar]
  4. Defendi V. Transformation in vitro of mammalian cells by polyoma and Simian 40 viruses. Prog Exp Tumor Res. 1966;8:125–188. doi: 10.1159/000386007. [DOI] [PubMed] [Google Scholar]
  5. Ellims P. H., Hayman R. J., Van der Weyden M. B. Expression of fetal thymidine kinase in human cobalamin or folate deficient lymphocytes. Biochem Biophys Res Commun. 1979 Jul 12;89(1):103–107. doi: 10.1016/0006-291x(79)90949-5. [DOI] [PubMed] [Google Scholar]
  6. Galloway D. R., McCabe R. P., Pellegrino M. A., Ferrone S., Reisfeld R. A. Tumor-associated antigens in spent medium of human melanoma cells: immunochemical characterization with xenoantisera. J Immunol. 1981 Jan;126(1):62–66. [PubMed] [Google Scholar]
  7. Glovanella B. C., Stehlin J. S., Santamaria C., Yim S. O., Morgan A. C., Williams L. J., Jr, Leibovitz A., Fialkow P. J., Mumford D. M. Human neoplastic and normal cells in tissue culture. I. Cell lines derived from malignant melanomas and normal melanocytes. J Natl Cancer Inst. 1976 Jun;56(6):1131–1142. doi: 10.1093/jnci/56.6.1131. [DOI] [PubMed] [Google Scholar]
  8. Granatek C. H., Scheinberg B. M., Corry P. M. Unmasking of fetal determinants on adult bone marrow cells. Nature. 1979 Oct 11;281(5731):484–485. doi: 10.1038/281484a0. [DOI] [PubMed] [Google Scholar]
  9. Gupta R. K., Irie R. F., Chee D. O., Kern D. H., Morton D. L. Demonstration of two distinct antigens in spent tissue culture medium of a human malignant melanoma cell line. J Natl Cancer Inst. 1979 Aug;63(2):347–356. [PubMed] [Google Scholar]
  10. Gupta R. K., Silver H. K., Reisfeld R. A., Morton D. L. Isolation and immunochemical characterization of antibodies from the sera of cancer patients which are reactive against human melanoma cell membranes by affinity chromatography. Cancer Res. 1979 May;39(5):1683–1695. [PubMed] [Google Scholar]
  11. Imai K., Molinaro G. A., Ferrone S. Monoclonal antibodies to human melanoma-associated antigens. Transplant Proc. 1980 Sep;12(3):380–383. [PubMed] [Google Scholar]
  12. Irie R. F., Irie K., Morton D. L. A membrane antigen common to human cancer and fetal brain tissues. Cancer Res. 1976 Sep;36(9 Pt 2):3510–3517. [PubMed] [Google Scholar]
  13. Jerry L. M., Lewis M. G., Rowden G., Sullivan A. K., Pitzele R., Law T. Fetal antigens in nonneoplastic conditions. Cancer Res. 1976 Sep;36(9 Pt 2):3446–3452. [PubMed] [Google Scholar]
  14. Kessler S. W. Rapid isolation of antigens from cells with a staphylococcal protein A-antibody adsorbent: parameters of the interaction of antibody-antigen complexes with protein A. J Immunol. 1975 Dec;115(6):1617–1624. [PubMed] [Google Scholar]
  15. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  16. Lever J. E. Modulation of glucose uptake in animal cells. Studies using plasma membrane vesicles isolated from nontransformed and simian virus 40-transformed mouse fibroblast cultures. J Biol Chem. 1979 Apr 25;254(8):2961–2967. [PubMed] [Google Scholar]
  17. Lewis M. G., Ikonopisov R. L., Nairn R. C., Phillips T. M., Fairley G. H., Bodenham D. C., Alexander P. Tumour-specific antibodies in human malignant melanoma and their relationship to the extent of the disease. Br Med J. 1969 Sep 6;3(5670):547–552. doi: 10.1136/bmj.3.5670.547. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lewis M. G., Rowden G., Sheikh K. M. Foetal-associated material: its expression in long-term cultured human skin. Differentiation. 1975 Aug 11;3(1-3):149–154. doi: 10.1111/j.1432-0436.1975.tb00855.x. [DOI] [PubMed] [Google Scholar]
  19. Lewis M. G., Sheikh K. M., Avis P., Whitehead V. M., Vera C. The indentification of foetal antigens in human bone marrow cells. Differentiation. 1974 Oct;2(5):307–311. doi: 10.1111/j.1432-0436.1974.tb00365.x. [DOI] [PubMed] [Google Scholar]
  20. McCabe R. P., Ferrone S., Pellegrino M. A., Kern D. H., Holmes E. C., Reisfeld R. A. Purification and immunologic evaluation of human melnoma-associated antigens. J Natl Cancer Inst. 1978 Apr;60(4):773–777. doi: 10.1093/jnci/60.4.773. [DOI] [PubMed] [Google Scholar]
  21. Morgan A. C., Jr, Galloway D. R., Imai K., Reisfeld R. A. Human melanoma-associated antigens: role of carbohydrate in shedding and cell surface expression. J Immunol. 1981 Jan;126(1):365–370. [PubMed] [Google Scholar]
  22. Morgan A. C., Jr, Galloway D. R., Wilson B. S., Reisfeld R. A. Human melanoma associated antigens: a solid-phase assay for detection of specific antibody. J Immunol Methods. 1980;39(3):233–246. doi: 10.1016/0022-1759(80)90058-7. [DOI] [PubMed] [Google Scholar]
  23. Morton D. L., Malmgren R. A., Holmes E. C., Ketcham A. S. Demonstration of antibodies against human malignant melanoma by immunofluorescence. Surgery. 1968 Jul;64(1):233–240. [PubMed] [Google Scholar]
  24. Patt L. M., Grimes W. J. Cell surface glycolipid and glycoprotein glycosyltransferases of normal and transformed cells. J Biol Chem. 1974 Jul 10;249(13):4157–4165. [PubMed] [Google Scholar]
  25. Risser R., Pollack R. A nonselective analysis of SV40 transformation of mouse 3T3 cells. Virology. 1974 Jun;59(2):477–489. doi: 10.1016/0042-6822(74)90457-7. [DOI] [PubMed] [Google Scholar]
  26. Rothman J. E., Katz F. N., Lodish H. F. Glycosylation of a membrane protein is restricted to the growing polypeptide chain but is not necessary for insertion as a transmembrane protein. Cell. 1978 Dec;15(4):1447–1454. doi: 10.1016/0092-8674(78)90068-5. [DOI] [PubMed] [Google Scholar]
  27. Ruoslahti E., Engvall E. Immunochemical and collagen-binding properties of fibronectin. Ann N Y Acad Sci. 1978 Jun 20;312:178–191. doi: 10.1111/j.1749-6632.1978.tb16802.x. [DOI] [PubMed] [Google Scholar]
  28. Shiku H., Takahashi T., Oettgen H. F. Cell surface antigens of human malignant melanoma. II. Serological typing with immune adherence assays and definition of two new surface antigens. J Exp Med. 1976 Oct 1;144(4):873–881. doi: 10.1084/jem.144.4.873. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Steplewski Z., Herlyn M., Herlyn D., Clark W. H., Koprowski H. Reactivity of monoclonal anti-melanoma antibodies with melanoma cells freshly isolated from primary and metastatic melanoma. Eur J Immunol. 1979 Jan;9(1):94–96. doi: 10.1002/eji.1830090120. [DOI] [PubMed] [Google Scholar]
  30. Stiles C. D., Desmond W., Jr, Sato G., Saier M. H., Jr Failure of human cells transformed by simian virus 40 to form tumors in athymic nude mice. Proc Natl Acad Sci U S A. 1975 Dec;72(12):4971–4975. doi: 10.1073/pnas.72.12.4971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Stonehill E. H., Bendich A. Retrogenetic expression: the reappearance of embryonal antigens in cancer cells. Nature. 1970 Oct 24;228(5269):370–372. doi: 10.1038/228370a0. [DOI] [PubMed] [Google Scholar]
  32. Thorpe W. P., Parker G. A., Rosenberg S. A. Expression of fetal antigens by normal human skin cells grown in tissue culture. J Immunol. 1977 Sep;119(3):818–823. [PubMed] [Google Scholar]
  33. Warren L., Buck C. A., Tuszynski G. P. Glycopeptide changes and malignant transformation. A possible role for carbohydrate in malignant behavior. Biochim Biophys Acta. 1978 Sep 18;516(1):97–127. doi: 10.1016/0304-419x(78)90005-7. [DOI] [PubMed] [Google Scholar]
  34. Woodbury R. G., Brown J. P., Yeh M. Y., Hellström I., Hellström K. E. Identification of a cell surface protein, p97, in human melanomas and certain other neoplasms. Proc Natl Acad Sci U S A. 1980 Apr;77(4):2183–2187. doi: 10.1073/pnas.77.4.2183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Zeuthen J., Nørgaard J. O., Avner P., Fellous M., Wartiovaara J., Vaheri A., Rosén A., Giovanella B. C. Characterization of a human ovarian teratocarcinoma-derived cell line. Int J Cancer. 1980 Jan 15;25(1):19–32. doi: 10.1002/ijc.2910250104. [DOI] [PubMed] [Google Scholar]

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