Abstract
The expression of a high-Mr sialogalactoprotein (gp580) on rat 13762NF mammary adenocarcinoma cells was identified and correlated with spontaneous metastatic potential to colonize lung [Steck & Nicolson (1983) Exp. Cell Res. 147, 255-267]. Using a highly metastatic tumour-cell clone, MTLn3, we isolated and characterized gp580 from cells growing in vitro and in vivo in the mammary fat-pads of Fischer 344 rats. The glycoprotein was extracted with 4 M-guanidinium chloride/4% Zwittergent 3-12 solution in the presence of proteinase inhibitors. The extracts were then subjected to dissociative CsCl-density-gradient centrifugation, gel filtration on Sepharose CL-2B columns and ion-exchange chromatography on DEAE-Sephacel. The isolated glycoprotein possessed low electrophoretic mobility in SDS/polyacrylamide gels, and after desialylation bound 125I-labelled peanut agglutinin. Electrophoresis of gp580 in polyacrylamide-gradient gels resulted in a diffuse but homogeneous migrating band of Mr approx. 55,000. After removal of carbohydrate, gp580 was demonstrated to have a protein core of Mr approx. 150,000. The gp580 had a high density (1.430 g/ml) on isopycnic centrifugation in 4 M-guanidinium chloride and was resistant to most proteinases and other degradative enzymes, suggesting a mucin-like structure. Amino acid and carbohydrate analyses revealed that gp580 has high contents of serine, threonine, glutamic acid, aspartic acid, glucosamine and galactosamine; several acidic and neutral oligosaccharides were obtained from alkaline-borohydride digests. Cellular localization studies suggested that gp580 is associated mainly with the cell-surface and extracellular-matrix fractions of MTLn3 cells.
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- Alexander P. Proceedings: Escape from immune destruction by the host through shedding of surface antigens: is this a characteristic shared by malignant and embryonic cells? Cancer Res. 1974 Aug;34(8):2077–2082. [PubMed] [Google Scholar]
- Baumann G., Chrambach A. A highly crosslinked, transparent polyacrylamide gel with improved mechanical stability for use in isoelectric focusing and isotachophoresis. Anal Biochem. 1976 Jan;70(1):32–38. doi: 10.1016/s0003-2697(76)80044-9. [DOI] [PubMed] [Google Scholar]
- Behnke J. N., Dagher S. M., Massey T. H., Deal W. C., Jr Rapid, multisample isoelectric focusing in sucrose density gradients using conventional polyacrylamide electrophoresis equpiment: a two-peak transient in the approach-to-equilibrium. Anal Biochem. 1975 Nov;69(1):1–9. doi: 10.1016/0003-2697(75)90558-8. [DOI] [PubMed] [Google Scholar]
- Bhavanandan V. P., Umemoto J., Banks J. R., Davidson E. A. Isolation and partial characterization of sialoglycopeptides produced by a murine melanoma. Biochemistry. 1977 Oct 4;16(20):4426–4437. doi: 10.1021/bi00639a016. [DOI] [PubMed] [Google Scholar]
- Burridge K. Changes in cellular glycoproteins after transformation: identification of specific glycoproteins and antigens in sodium dodecyl sulfate gels. Proc Natl Acad Sci U S A. 1976 Dec;73(12):4457–4461. doi: 10.1073/pnas.73.12.4457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carlson D. M. Structures and immunochemical properties of oligosaccharides isolated from pig submaxillary mucins. J Biol Chem. 1968 Feb 10;243(3):616–626. [PubMed] [Google Scholar]
- Chatterjee S. K., Kim U. Fucosyltransferase activity in metastasizing and nonmetastasizing rat mammary carcinomas. J Natl Cancer Inst. 1978 Jul;61(1):151–162. doi: 10.1093/jnci/61.1.151. [DOI] [PubMed] [Google Scholar]
- Chernoff E. A., Maresh G. A., Culp L. A. Isolation and characterization of a large, neurite-associated glycoconjugate from neuroblastoma cells. J Cell Biol. 1983 Mar;96(3):661–668. doi: 10.1083/jcb.96.3.661. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cooper A. G., Codington J. F., Brown M. C. In vivo release of glycoprotein I from the Ha subline of TA3 murine tumor into ascites fluid and serum. Proc Natl Acad Sci U S A. 1974 Apr;71(4):1224–1228. doi: 10.1073/pnas.71.4.1224. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Edge A. S., Faltynek C. R., Hof L., Reichert L. E., Jr, Weber P. Deglycosylation of glycoproteins by trifluoromethanesulfonic acid. Anal Biochem. 1981 Nov 15;118(1):131–137. doi: 10.1016/0003-2697(81)90168-8. [DOI] [PubMed] [Google Scholar]
- HUNTER W. M., GREENWOOD F. C. Preparation of iodine-131 labelled human growth hormone of high specific activity. Nature. 1962 May 5;194:495–496. doi: 10.1038/194495a0. [DOI] [PubMed] [Google Scholar]
- Hascall V. C., Kimura J. H. Proteoglycans: isolation and characterization. Methods Enzymol. 1982;82(Pt A):769–800. doi: 10.1016/0076-6879(82)82102-2. [DOI] [PubMed] [Google Scholar]
- Herzberg M. C., Levine M. J., Ellison S. A., Tabak L. A. Purification and characterization of monkey salivary mucin. J Biol Chem. 1979 Mar 10;254(5):1487–1494. [PubMed] [Google Scholar]
- Howard S. C., Hull S. R., Huggins J. W., Carraway C. A., Carraway K. L. Relationship between xenotransplantability and cell surface properties of ascites sublines of a rat mammary adenocarcinoma. J Natl Cancer Inst. 1982 Jul;69(1):33–40. [PubMed] [Google Scholar]
- Hull S. R., Laine R. A., Kaizu T., Rodriguez I., Carraway K. L. Structures of the O-linked oligosaccharides of the major cell surface sialoglycoprotein of MAT-B1 and MAT-C1 ascites sublines of the 13762 rat mammary adenocarcinoma. J Biol Chem. 1984 Apr 25;259(8):4866–4877. [PubMed] [Google Scholar]
- Imam A., Laurence D. J., Neville A. M. Isolation and characterization of a major glycoprotein from milk-fat-globule membrane of human breast milk. Biochem J. 1981 Jan 1;193(1):47–54. doi: 10.1042/bj1930047. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Irimura T., Gonzalez R., Nicolson G. L. Effects of tunicamycin on B16 metastatic melanoma cell surface glycoproteins and blood-borne arrest and survival properties. Cancer Res. 1981 Sep;41(9 Pt 1):3411–3418. [PubMed] [Google Scholar]
- Irimura T., Nicolson G. L. Carbohydrate chain analysis by lectin binding to electrophoretically separated glycoproteins from murine B16 melanoma sublines of various metastatic properties. Cancer Res. 1984 Feb;44(2):791–798. [PubMed] [Google Scholar]
- Johnson V. G., Schlom J., Paterson A. J., Bennett J., Magnani J. L., Colcher D. Analysis of a human tumor-associated glycoprotein (TAG-72) identified by monoclonal antibody B72.3. Cancer Res. 1986 Feb;46(2):850–857. [PubMed] [Google Scholar]
- 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]
- Kraemer P. M. Heparan sulfates of cultured cells. I. Membrane-associated and cell-sap species in Chinese hamster cells. Biochemistry. 1971 Apr 13;10(8):1437–1445. doi: 10.1021/bi00784a026. [DOI] [PubMed] [Google Scholar]
- 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]
- Liotta L. A., Tryggvason K., Garbisa S., Hart I., Foltz C. M., Shafie S. Metastatic potential correlates with enzymatic degradation of basement membrane collagen. Nature. 1980 Mar 6;284(5751):67–68. doi: 10.1038/284067a0. [DOI] [PubMed] [Google Scholar]
- Miller S. C., Hay E. D., Codington J. F. Ultrastructural and histochemical differences in cell surface properties of strain-specific and nonstrain-specific TA3 adenocarcinoma cells. J Cell Biol. 1977 Mar;72(3):511–529. doi: 10.1083/jcb.72.3.511. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nakajima M., Irimura T., Di Ferrante D., Di Ferrante N., Nicolson G. L. Heparan sulfate degradation: relation to tumor invasive and metastatic properties of mouse B16 melanoma sublines. Science. 1983 May 6;220(4597):611–613. doi: 10.1126/science.6220468. [DOI] [PubMed] [Google Scholar]
- Neri A., Welch D., Kawaguchi T., Nicolson G. L. Development and biologic properties of malignant cell sublines and clones of a spontaneously metastasizing rat mammary adenocarcinoma. J Natl Cancer Inst. 1982 Mar;68(3):507–517. [PubMed] [Google Scholar]
- Nicolson G. L. Cancer metastasis. Organ colonization and the cell-surface properties of malignant cells. Biochim Biophys Acta. 1982 Dec 21;695(2):113–176. doi: 10.1016/0304-419x(82)90020-8. [DOI] [PubMed] [Google Scholar]
- Nicolson G. L. Cell surface molecules and tumor metastasis. Regulation of metastatic phenotypic diversity. Exp Cell Res. 1984 Jan;150(1):3–22. doi: 10.1016/0014-4827(84)90696-7. [DOI] [PubMed] [Google Scholar]
- Nicolson G. L., Poste G. Tumor implantation and invasion at metastatic sites. Int Rev Exp Pathol. 1983;25:77–181. [PubMed] [Google Scholar]
- Poste G., Nicolson G. L. Arrest and metastasis of blood-borne tumor cells are modified by fusion of plasma membrane vesicles from highly metastatic cells. Proc Natl Acad Sci U S A. 1980 Jan;77(1):399–403. doi: 10.1073/pnas.77.1.399. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Raz A., McLellan W. L., Hart I. R., Bucana C. D., Hoyer L. C., Sela B. A., Dragsten P., Fidler I. J. Cell surface properties of B16 melanoma variants with differing metastatic potential. Cancer Res. 1980 May;40(5):1645–1651. [PubMed] [Google Scholar]
- Sherblom A. P., Buck R. L., Carraway K. L. Purification of the major sialoglycoproteins of 13762 MAT-B1 and MAT-C1 rat ascites mammary adenocarcinoma cells by density gradient centrifugation in cesium chloride and guanidine hydrochloride. J Biol Chem. 1980 Jan 25;255(2):783–790. [PubMed] [Google Scholar]
- Shimizu M., Yamauchi K. Isolation and characterization of mucin-like glycoprotein in human milk fat globule membrane. J Biochem. 1982 Feb;91(2):515–524. doi: 10.1093/oxfordjournals.jbchem.a133724. [DOI] [PubMed] [Google Scholar]
- Sloane B. F., Dunn J. R., Honn K. V. Lysosomal cathepsin B: correlation with metastatic potential. Science. 1981 Jun 5;212(4499):1151–1153. doi: 10.1126/science.7233209. [DOI] [PubMed] [Google Scholar]
- Sloane B. F., Honn K. V., Sadler J. G., Turner W. A., Kimpson J. J., Taylor J. D. Cathepsin B activity in B16 melanoma cells: a possible marker for metastatic potential. Cancer Res. 1982 Mar;42(3):980–986. [PubMed] [Google Scholar]
- Steck P. A., Nicolson G. L. Cell surface glycoproteins of 13762NF mammary adenocarcinoma clones of differing metastatic potentials. Exp Cell Res. 1983 Sep;147(2):255–267. doi: 10.1016/0014-4827(83)90208-2. [DOI] [PubMed] [Google Scholar]
- Sugarbaker E. V. Cancer metastasis: a product of tumor-host interactions. Curr Probl Cancer. 1979 Jan;3(7):1–59. doi: 10.1016/s0147-0272(79)80008-2. [DOI] [PubMed] [Google Scholar]
- Terranova V. P., Rao C. N., Kalebic T., Margulies I. M., Liotta L. A. Laminin receptor on human breast carcinoma cells. Proc Natl Acad Sci U S A. 1983 Jan;80(2):444–448. doi: 10.1073/pnas.80.2.444. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Van Lenten L., Ashwell G. Studies on the chemical and enzymatic modification of glycoproteins. A general method for the tritiation of sialic acid-containing glycoproteins. J Biol Chem. 1971 Mar 25;246(6):1889–1894. [PubMed] [Google Scholar]


