Heparin increases the adhesion of murine mammary adenocarcinoma cells (LM3). Correlation with the presence of heparin receptors on cell surface

Mastocytosis is a common feature around solid tumors. Due to mast cell (MC) degranulation, heparin and other chemical mediators are released to surrounding tissues. The aim of this paper is to investigate the role of heparin and chemically modified heparins, on a murine mammary adenocarcinoma cell l...

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Autor principal: Bertolesi, G.
Otros Autores: Eijan, A.M, Calvo, J.C, de Cidre, L.L
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Wichtig Editore s.r.l. 2005
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Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
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100 1 |a Bertolesi, G. 
245 1 0 |a Heparin increases the adhesion of murine mammary adenocarcinoma cells (LM3). Correlation with the presence of heparin receptors on cell surface 
260 |b Wichtig Editore s.r.l.  |c 2005 
270 1 0 |m de Cidre, L.L.; Laboratorio de Histología Animal, Departamento de Ciencias Biológicas, Universidad de Buenos Aires, Pab. II, 2do. piso, 1428 Buenos Aires, Argentina; email: laurial@bg.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
504 |a Theoharides, T.C., Conti, P., Mast cells: The JEKYLL and HYDE of tumor growth (2004) Trends in Immunology, 25, pp. 235-241 
504 |a Lauría de Cidre, L.S., Eijan, A.M., Bertolesi, G., Isturiz, M., Sacerdote de Lustig, E., Influence of mast cells on two murine mammary adenocarcinomas (1996) Tumour. Biol., 17, pp. 345-353 
504 |a Bertolesi, G.E., Stockert, J.C., Lauría de Cidre, L., Microfluorometry and image analysis of peritoneal mast cells reveals differences in the morphology and content of sulfated polyanions between normal and tumor-bearing mice (1997) Int. J. Oncol., 11, pp. 1221-1225 
504 |a Bertolesi, G.E., Lauria de Cidre, L., Eijan, A.M., Growth inhibition in vitro of murine mammary adenocarcinoma cells by heparin and chemically modified heparins (1994) Tumour. Biol., 15, pp. 275-283 
504 |a Bertolesi, G.E., Lauria de Cidre, L., Sacerdote de Lustig, E., Eijan, A.M., Heparin receptors in two murine mammary adenocarcinomas with different metastatic ability: Relationship with growth inhibition (1995) Cancer Letters, 90, pp. 123-131 
504 |a Alonso, D.F., Bertolesi, G.E., Farias, E.F., Eiján, A.M., Bal de Kier Joffé, E., Lauría de Cidre, L., Antimetastatic effects associated with anticoagulant properties of heparin and chemically modified heparin species in a mouse mammary tumor model (1996) Oncol. Reports, 3, pp. 219-222 
504 |a Engelberg, H., Actions of heparin that may affect the malignant process (1999) Cancer, 85, pp. 257-272 
504 |a Hulett, M.D., Freeman, C., Hamdorf, B.J., Baker, R.T., Harris, M.J., Parish, C.R., Cloning of mammalian heparanase, an important enzyme in tumor invasion and metastasis (1999) Nature, 5, pp. 803-809 
504 |a Borsig, L., Wong, R., Feramisco, J., Nadeau, D.R., Varki, N.M., Varki, A., Heparin and cancer revisited: Mechanistic connections involving platelets, P-selectin, carcinoma mucins, and tumor metastasis (2001) Proc. Natl. Acad. Sci. U. S. A., 98, pp. 3352-3357 
504 |a Ruoslahti, E., RGD and other recognition sequences for integrins (1996) Annu. Rev. Cell Dev. Biol., 12, pp. 697-715 
504 |a Chattopadhyay, N., Chatterjee, A., Studies on the expression of alpha(v)beta3 integrin receptors in non-malignant and malignant human cervical tumor tissues (2001) J. Exp. Clin. Cancer Res., 20, pp. 269-275 
504 |a LeBaron, R.G., Hook, A., Esko, J.D., Gay, S., Hook, M., Binding of heparan sulfate to type V collagen. A mechanism of cell- substrate adhesion (1989) J. Biol. Chem., 264, pp. 7950-7956 
504 |a Woods, A., Couchman, J.R., Heparan sulfate proteoglycans and signalling in cell adhesion (1992) Adv. Exp. Med. Biol., 313, pp. 87-96 
504 |a San Antonio, J.D., Slover, J., Lawler, J., Karnovsky, M.J., Lander, A.D., Specificity in the interactions of extracellular matrix proteins with subpopulations of the glycosaminoglycan heparin (1993) Biochemistry, 32, pp. 4746-4755 
504 |a Savage, J.M., Gilotti, A.C., Granzow, C.A., Molina, F., Lowe-Krentz, L.J., Antibodies against a putative heparin receptor slow cell proliferation and decrease MAPK activation in vascular smooth muscle cells (2001) J. Cell Physiol., 187, pp. 283-293 
504 |a Castellot Jr., J.J., Wong, K., Herman, B., Binding and internalization of heparin by vascular smooth muscle cells (1985) J. Cell Physiol., 124, pp. 13-20 
504 |a Bilozur, M.E., Biswas, C., Identification and characterization of heparan sulfate-binding proteins from human lung carcinoma cells (1990) J. Biol. Chem., 265, pp. 19697-19703 
504 |a Redini, F., Moczar, E., Antoine, E., Poupon, M.F., Binding and internalization of exogenous glycosaminoglycans in weakly and highly metastatic rhabdomyosarcoma cells (1989) Biochim. Biophys. Acta, 991, pp. 359-366 
504 |a Pukac, L.A., Castellot Jr., J.J., Wright Jr., T.C., Caleb, B.L., Karnovsky, M.J., Heparin inhibits c-fos and c-myc mRNA expression in vascular smooth muscle cells (1990) Cell Regul., 1, pp. 435-443 
504 |a Templeton, D.M., Zhao, Y., Fan, M.Y., Heterogeneity in the response of vascular smooth muscle to heparin: Altered signaling in heparin-resistant cells (2000) Cardiovasc. Res., 45, pp. 503-512 
504 |a Rozenberg, G., Espada, J., Lauria de Cidre, L., Eijan, A.M., Calvo, J.C., Bertolesi, G.E., Heparan sulfate, heparin and heparinase activity detection on polyacrilamide gel electrophoresis using a fluorochrome tris (2, 2′-bipyridine)ruthenium (II) (2001) Electrophoresis, 22, pp. 3-11 
504 |a Bal de Kier Joffe, E., Puricelli, L., Sacerdote de Lustig, E., Modified adhesion behavior after in vitro passage of two related murine mammary adenocarcinomas with different metastasizing ability (1986) Invasion Metastasis, 6, pp. 302-312 
504 |a Labarca, C., Paigen, K., A simple, rapid, and sensitive DNA assay procedure (1980) Anal. Biochem., 102, pp. 344-352 
504 |a Lundmark, K., Tran, P.K., Kinsella, M.G., Clowes, A.W., Wight, T.N., Hedin, U., Perlecan inhibits smooth muscle cell adhesion to fibronectin: Role of heparan sulfate (2001) J. Cell Physiol., 188, pp. 67-74 
504 |a Iozzo, R.V., Proteoglycans and neoplasia (1988) Cancer & Met. Rev., 7, pp. 39-50 
504 |a Lindahl, U., Thunberg, L., Backstrom, G., Riesenfeld, J., Nordling, K., Bjork, I., Extension and structural variability of the antithrombin-binding sequence in heparin (1984) J. Biol. Chem., 259, pp. 12368-12376 
504 |a Koyama, N., Kinsella, M.G., Wight, T.N., Hedin, U., Clowes, A.W., Heparan sulfate proteoglycans mediate inhibitory signal for migration of vascular smooth muscle cells (1988) Circ. Res., 83 (3), pp. 305-313 
504 |a Culp, L.A., Rollins, B.J., Buniel, J., Hitri, S., Two functionally distinct pools of glycosaminoglycan in the substrate adhesion site of murine cells (1978) J. Cell Biol., 79, pp. 788-801 
504 |a Miura, R., Aspberg, A., Ethell, I.M., The proteoglycan lectin domain binds sulfated cell surface glycolipids and promotes cell adhesion (1999) J. Biol. Chem., 274, pp. 11431-11438 
504 |a Puleo, D.A., Bizios, R., RGDS tetrapeptide binds to osteoblasts and inhibits fibronectin- mediated adhesion (1991) Bone, 12, pp. 271-276 
504 |a Lauría de Cidre, L., Sacerdote de Lustig, E., Mast cell kinetics during tumor growth 196-201 (1990) Tumor. Biol., 11 
520 3 |a Mastocytosis is a common feature around solid tumors. Due to mast cell (MC) degranulation, heparin and other chemical mediators are released to surrounding tissues. The aim of this paper is to investigate the role of heparin and chemically modified heparins, on a murine mammary adenocarcinoma cell line adhesion properties, and the relationship with the presence of heparin binding sites in tumor cells. We show that heparin increases tumor cell adhesion in a dose-dependent manner. When the number of heparin binding sites was regulated, by culturing the cells with different FCS concentration for 24 hours, a correlation between binding capacity and heparin effect on cell adhesion was observed. The increment on cell adhesion by heparin was lower on cells with less heparin binding sites. Moreover, only heparin and a chemically modified heparin (partially N-desulfated N-acetylated), which bound to heparin-receptor, retained the ability to stimulate cell adhesion, while other modified heparins lost both effects. The increase in cell adhesion was observed on plastic dishes, albumin, as well as on fibronectin pre-coated ones suggesting that heparin effect is substratum independent. Our results show a direct relation between heparin binding to specific cell receptors and increase in cell attachment. © Wichtig Editore, 2005.  |l eng 
593 |a Facultad de Ciencias Exactas y Naturales, Departamento de Biodiversidad y Biología Experimental, Universidad de Buenos Aires, Pab. II, 2do. piso, 1428 Buenos Aires, Argentina 
650 1 7 |2 spines  |a ADHESION 
690 1 0 |a CELL RECEPTOR 
690 1 0 |a FIBRONECTIN 
690 1 0 |a HEPARIN 
690 1 0 |a TUMOR 
690 1 0 |a ALBUMIN 
690 1 0 |a CELL RECEPTOR 
690 1 0 |a FIBRONECTIN 
690 1 0 |a HEPARIN 
690 1 0 |a HEPARIN DERIVATIVE 
690 1 0 |a TRITIUM 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ARTICLE 
690 1 0 |a BINDING AFFINITY 
690 1 0 |a BINDING SITE 
690 1 0 |a BREAST ADENOCARCINOMA 
690 1 0 |a CANCER CELL CULTURE 
690 1 0 |a CELL ADHESION 
690 1 0 |a CELL STIMULATION 
690 1 0 |a CELL SURFACE 
690 1 0 |a CONCENTRATION RESPONSE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a CORRELATION ANALYSIS 
690 1 0 |a DRUG RECEPTOR BINDING 
690 1 0 |a MOUSE 
690 1 0 |a NONHUMAN 
690 1 0 |a MURINAE 
700 1 |a Eijan, A.M. 
700 1 |a Calvo, J.C. 
700 1 |a de Cidre, L.L. 
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