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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
. 1977 Jul;74(7):3011–3013. doi: 10.1073/pnas.74.7.3011

Glycolipid-bound sialic acid in serum: increased levels in mice and humans bearing mammary carcinomas.

T M Kloppel, T W Keenan, M J Freeman, D J Morré
PMCID: PMC431387  PMID: 268648

Abstract

In mice bearing transplantable mammary carcinomas, serum levels of sialic acid-containing glycolipids were elevated 2.5-fold in pooled serum samples from which gangliosides were purified by column chromatography. A method is also described by which ganglioside content was estimated on as little as 1.0 ml of whole blood to permit studies with individual tumor-bearing mice and age- and litter-matched controls. Using this method, we observed similar elevations in ganglioside levels that were independent of age and sex of the animal and appeared in advance of palpable tumors. Following excision of the tumors, the glycolipid sialic acid values dropped below control levels and remained there. Serum sialic acid of the glycolipid fraction was elevated nearly 2-fold in human carcinoma patients and appeared to decline after surgery.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Amano T., Richelson E., Nirenberg M. Neurotransmitter synthesis by neuroblastoma clones (neuroblast differentiation-cell culture-choline acetyltransferase-acetylcholinesterase-tyrosine hydroxylase-axons-dendrites). Proc Natl Acad Sci U S A. 1972 Jan;69(1):258–263. doi: 10.1073/pnas.69.1.258. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barkal A., Di Cesare J. L. Influence of sialic acid groups on the retention of glycosphingolipids in blood plasma. Biochim Biophys Acta. 1975 Aug 25;398(2):287–293. doi: 10.1016/0005-2760(75)90144-7. [DOI] [PubMed] [Google Scholar]
  3. Bernacki R. J., Kim U. Concomitant elevations in serum sialytransferase activity and sialic acid content in rats with metastasizing mammary tumors. Science. 1977 Feb 11;195(4278):577–580. doi: 10.1126/science.835014. [DOI] [PubMed] [Google Scholar]
  4. Brady R. O., Fishman P. H. Biosynthesis of glycolipids in virus-transformed cells. Biochim Biophys Acta. 1974 Sep 9;355(2):121–148. doi: 10.1016/0304-419x(74)90001-8. [DOI] [PubMed] [Google Scholar]
  5. Buck C. A., Glick M. C., Warren L. Glycopeptides from the surface of control and virus-transformed cells. Science. 1971 Apr 9;172(3979):169–171. doi: 10.1126/science.172.3979.169. [DOI] [PubMed] [Google Scholar]
  6. Dawson G., Kruski A. W., Scanu A. M. Distribution of glycosphingolipids in the serum lipoproteins of normal human subjects and patients with hypo- and hyperlipidemias. J Lipid Res. 1976 Mar;17(2):125–131. [PubMed] [Google Scholar]
  7. Glick M. C., Buck C. A. Glycoproteins from the surface of metaphase cells. Biochemistry. 1973 Jan 2;12(1):85–90. doi: 10.1021/bi00725a016. [DOI] [PubMed] [Google Scholar]
  8. Hakomori S. Structures and organization of cell surface glycolipids dependency on cell growth and malignant transformation. Biochim Biophys Acta. 1975 Mar 20;417(1):55–89. doi: 10.1016/0304-419x(75)90008-6. [DOI] [PubMed] [Google Scholar]
  9. Keenan T. W., Huang C. M., Morré D. J. Gangliosides: nonspecific localization in the surface membranes of bovine mammary gland and rat liver. Biochem Biophys Res Commun. 1972 Jun 28;47(6):1277–1283. doi: 10.1016/0006-291x(72)90211-2. [DOI] [PubMed] [Google Scholar]
  10. Keenan T. W., Morré D. James, Huang C. M. Distribution of gangliosides among subcellular fractions from rat liver and bovine mammary gland. FEBS Lett. 1972 Aug 1;24(2):204–208. doi: 10.1016/0014-5793(72)80768-3. [DOI] [PubMed] [Google Scholar]
  11. Kim U., Baumler A., Carruthers C., Bielat K. Immunological escape mechanism in spontaneously metastasizing mammary tumors. Proc Natl Acad Sci U S A. 1975 Mar;72(3):1012–1016. doi: 10.1073/pnas.72.3.1012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Ledeen R. W., Yu R. K., Eng L. F. Gangliosides of human myelin: sialosylgalactosylceramide (G7) as a major component. J Neurochem. 1973 Oct;21(4):829–839. doi: 10.1111/j.1471-4159.1973.tb07527.x. [DOI] [PubMed] [Google Scholar]
  13. Richardson C. L., Baker S. R., Morré D. J., Keenan T. W. Glycosphingolipid synthesis and tumorigenesis. A role for the Golgi apparatus in the origin of specific receptor molecules of the mammalian cell surface. Biochim Biophys Acta. 1975 Dec 31;417(3-4):175–186. doi: 10.1016/0304-419x(75)90009-8. [DOI] [PubMed] [Google Scholar]
  14. Roseman S. The synthesis of complex carbohydrates by multiglycosyltransferase systems and their potential function in intercellular adhesion. Chem Phys Lipids. 1970 Oct;5(1):270–297. doi: 10.1016/0009-3084(70)90024-1. [DOI] [PubMed] [Google Scholar]
  15. Skipski V. P., Barclay M., Archibald F. M., Stock C. C. Tumor proteolipids. Prog Biochem Pharmacol. 1975;10:112–134. [PubMed] [Google Scholar]
  16. Skipski V. P., Katopodis N., Prendergast J. S., Stock C. C. Gangliosides in blood serum of normal rats and Morris hepatoma 5123tc-bearing rats. Biochem Biophys Res Commun. 1975 Dec 1;67(3):1122–1127. doi: 10.1016/0006-291x(75)90790-1. [DOI] [PubMed] [Google Scholar]
  17. Van Beek W. P., Smets L. A., Emmelot P. Changed surface glycoprotein as a marker of malignancy in human leukaemic cells. Nature. 1975 Feb 6;253(5491):457–460. doi: 10.1038/253457a0. [DOI] [PubMed] [Google Scholar]
  18. WARREN L. The thiobarbituric acid assay of sialic acids. J Biol Chem. 1959 Aug;234(8):1971–1975. [PubMed] [Google Scholar]
  19. WEBSTER G. R., FOLCH J. Some studies on the properties of proteolipids. Biochim Biophys Acta. 1961 May 13;49:399–401. doi: 10.1016/0006-3002(61)90144-5. [DOI] [PubMed] [Google Scholar]
  20. Warren L., Critchley D., Macpherson I. Surface glycoproteins and glycolipids of chicken embryo cells transformed by a temperature-sensitive mutant of Rous sarcoma virus. Nature. 1972 Feb 4;235(5336):275–278. doi: 10.1038/235275a0. [DOI] [PubMed] [Google Scholar]
  21. Warren L., Fuhrer J. P., Buck C. A. Surface glycoproteins of cells before and after transformation by oncogenic viruses. Fed Proc. 1973 Jan;32(1):80–85. [PubMed] [Google Scholar]
  22. Wiegandt H. Gangliosides of extraneural organs. Hoppe Seylers Z Physiol Chem. 1973 Sep;354(9):1049–1056. doi: 10.1515/bchm2.1973.354.2.1049. [DOI] [PubMed] [Google Scholar]
  23. Yamada K. M., Weston J. A. The synthesis, turnover, and artificial restoration of a major cell surface glycoprotein. Cell. 1975 May;5(1):75–81. doi: 10.1016/0092-8674(75)90094-x. [DOI] [PubMed] [Google Scholar]

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