Heparin receptors in two murine mammary adenocarcinomas with different metastatic ability: relationship with growth inhibition

Binding of heparin to primary cultured cells of two murine mammary adenocarcinomas with low (M3) and high (MM3) lung, metastatic capacity was determined. Heparin binding was rapid, specific and saturable. MM3 cells grown for 24 h in fetal calf serum (FCS)-free medium exhibited a higher number of bin...

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Autor principal: Bertolesix, G.E
Otros Autores: de Cidre, L.L, de Lustig, E.S, Eiján, A.M
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1995
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
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024 7 |2 scopus  |a 2-s2.0-0029062443 
024 7 |2 cas  |a Antineoplastic Agents; heparin receptor; Heparin, 9005-49-6; Receptors, Cell Surface 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a CALED 
100 1 |a Bertolesix, G.E. 
245 1 0 |a Heparin receptors in two murine mammary adenocarcinomas with different metastatic ability: relationship with growth inhibition 
260 |c 1995 
270 1 0 |m Bertolesix, G.E.; Area Investigación, Institute de Oncologia A.H. Roffo, Universidad de Buenos Aires, Av. San Martín 5481, Buenos Aires, 1417, Argentina 
506 |2 openaire  |e Política editorial 
504 |a Bal de Kier Joffé, Puricelli, Vidal, Sacerdote de Lustig, Characterization of two murine mammary adenocarcinoma tumors with different metastatic ability (1983) J. Exp. Clin. Cancer Res., 2, pp. 151-160 
504 |a Bal de Kier Joffé, Puricelli, Sacerdote de Lustig, Modified adhesion behaivour after in vitro passage of two-related murine mammary adenocarcinomas with different metastasizing ability (1986) Invasion Metastasis, 6, pp. 302-312 
504 |a Bertolesi, Lauria de Cidre, Eiján, Growth inhibition in vitro of murine mammary adenocarcinoma cells by heparin and chemically modified heparins (1994) Tumor Biol., 15, pp. 275-283 
504 |a Biswas, Heparin and heparan sulfate binding sites on B16 melanoma cells (1988) J. Cell. Physiol., 136, pp. 147-153 
504 |a Castellot, Beeker, Rosenberg, Karnovsky, Structural determinants of the capacity of heparin to inhibit the proliferation of vascular smooth muscle cells (1984) J. Cell. Physiol., 120, pp. 315-320 
504 |a Castellot, Wong, Herman, Hoover, Albertini, Wrigth, Caleb, Karnovsky, Binding and internalization of heparin by vascular smooth muscle cells (1985) J. Cell. Physiol., 124, pp. 13-20 
504 |a Castellot, Pukac, Caleb, Wrigth, Karnovsky, Heparin selectively inhibits a protein kinase C-dependent mechanism of cell cycle progression in calf aortic smooth muscle cells (1989) J. Cell Biol., 109, pp. 3147-3155 
504 |a Clowes, Karnovsy, Suppression by heparin of smooth muscle cell proliferation in injured arteries (1977) Nature, 265, pp. 625-626 
504 |a Evans, Marshall, Christey, Carrel, Heparin binding site, conformational change and activition of antithrombin (1992) Biochemistry, 31, pp. 12629-12642 
504 |a Glimelius, Busch, Hook, Binding of heparin on the surface of cultured human endothelial cells (1978) Tromb. Res., 12, pp. 773-782 
504 |a Halper, Carter, Modulation of growth of human carcinoma SW-13 cells by heparin and growth factors (1989) J. Cell. Physiol., 141, pp. 16-23 
504 |a Iozzo, Proteoglycans and neoplasia (1988) Cancer Metastasis Rev., 7, pp. 39-50 
504 |a Kjellen, Oldberg, Rubin, Hook, Binding of heparin and heparan sulfate to rat liver cells (1977) Biochem. Biophys. Res. Commun., 74, pp. 126-133 
504 |a Lindahl, Bñckström, Thunberg, The antithrombin-binding sequence in heparin. Identification of an essential 6-O-sulfate group (1983) J. Biol. Chem., 16, pp. 9826-9830 
504 |a Labarca, Paigen, A simple, rapid and sensitive DNA assay procedure (1980) Anal. Biochem., 102, pp. 344-352 
504 |a Ladeda, Puricelli, Urtreger, Alonso, Kornblihtt, Ball de Kier Joffé, Acción del Suero y de Inhibidores Proteásicos Sobre la Expresión in vitro de Fibronectina (1994) VI Congreso de La Sociedad Argentina de Ciencias Morfológicas, p. 91a 
504 |a Leung, Katsuyasu, Grant, Heparin binds to human monocytes and modulates their procoagulant activities and secretory phenotypes. Effect of histidine-rich glycoprotein (1989) Blood, 73, pp. 177-184 
504 |a Muro, Puricelli, Kornblihtt, Bal de Kier Joffe, Inverse correlation between fibronectin mRNA levels and the metastatic potential of two murine mammary adenocarcinomas (1991) Invation Metastasis, 11, pp. 281-287 
504 |a Ottlinger, Pukac, Karnovsky, Heparin inhibits mitogenic actived protein kinase activation in intact rat vascular smooth muscle cells (1993) J. Biol. Chem., 268, pp. 19173-19176 
504 |a Oyama, Eagle, Measurament of cell growth in tissue culture with phenol reagent (folinciocalteau) (1956) Proc. Soc. Exp. Biol. Med., 91, pp. 305-307. , Ed. 2 
504 |a Pereyra-Alfonso, Haedo, Bal de Kier Joffé, Correlation betwen urokinase-type plasminogen activator production and the metastasizing ability of two murine mammary adenocarcinomas (1988) Int. J. Cancer, 42, pp. 59-63 
504 |a Pukac, Castellot, Wrigth, Caleb, Karnovsky, Heparin inhibits c-fos and c-myc mRNA expression in vascular smooth muscle cells (1990) Cell Regul, 1, pp. 435-443 
504 |a Pukac, Ottlinger, Karnovsky, Heparin supresses specific second messenger pathways for protooncogene expression in rat vascular smooth muscle cells (1992) J. Biol. Chem., 267, pp. 3707-3711 
504 |a Redini, Moczar, Antoine, Poupon, Binding and internalization of exogenous glycosaminoglicans in weakly and highly metastatic rhabdomyosarcoma cells (1989) Biochem. Biophys. Acta, 991, pp. 359-366 
504 |a Reilly, Fritze, Rosenberg, Heparin-Like molecules regulate the number of epidermal growth factors on vascular smooth muscle cell (1988) Journal of Cellular Physiology, 136, pp. 26-32 
504 |a Reilly, Kindy, Brown, Rosenberg, Sonenshein, Heparin prevents vascular smooth muscle cell progression through the G1 phase of the cell cycle (1989) J. Biol. Chem., 264, pp. 6990-6995 
504 |a San Antonio, Slover, Lawler, Karnovsky, Lander, Specificity in the interactions of extracellular matrix proteins with subpopulations of the glycosaminoglycan heparin (1993) Biochem., 32, pp. 4746-4755 
504 |a Wrigth, Jr., Pukac, Castellot, Karnovsky, Levine, Kim-Park, Campisi, Heparin suppresses the induction of c-fos and c-myc mRNA in murine fibroblasts by selective inhibition of a protein kinase C-dependent pathway (1989) Proceedings of the National Academy of Sciences, 86, pp. 3199-3203. , Ed. 2 
520 3 |a Binding of heparin to primary cultured cells of two murine mammary adenocarcinomas with low (M3) and high (MM3) lung, metastatic capacity was determined. Heparin binding was rapid, specific and saturable. MM3 cells grown for 24 h in fetal calf serum (FCS)-free medium exhibited a higher number of binding sites for 3H-heparin [(11 ± 1) × 105 sites per cell] than M3 cells [(6.9 ± 0.6) × 105 sites per cell]. However, when M3 cells were grown in the presence of 2% FCS, they showed less heparin binding sites [(3.5 ± 0.4) × 105 sites per cell]. In contrast, dissociation constants were very similar for MM3 and M3 cells grown with or without FCS (Kd = 2-4 × 10-9M). Furthermore, heparin inhibited MM3 and M3 cell growth both in the absence or presence of FCS. Competition studies showed that chemically modified heparins lacking antiproliferative effect (O-desulfated; O/N-desulfated N-acetylated and N-desulfated heparins) were not able to inhibit 3H-heparin binding. N-desulfated N-acetylated heparin, which had partial antiproliferative effect, partially inhibited 3H-heparin binding, while heparin with a high antiproliferative activity inhibited more than 90% 3H-heparin binding. The antiproliferative effect of heparin and chemically modified heparins seems to be related to their binding ability to the cell membrane. © 1995.  |l eng 
593 |a Area Investigación, Institute de Oncologia A.H. Roffo, Universidad de Buenos Aires, Av. San Martín 5481, Buenos Aires, 1417, Argentina 
593 |a Laboratorio de Histologia Animal, Departamento de Biologia, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellon II, Buenos Aires 1428, Argentina, Argentina 
690 1 0 |a GROWTH INHIBITION 
690 1 0 |a HEPARIN 
690 1 0 |a METASTASIS 
690 1 0 |a RECEPTOR 
690 1 0 |a TUMOR 
690 1 0 |a HEPARIN 
690 1 0 |a MEMBRANE RECEPTOR 
690 1 0 |a TRITIUM 
690 1 0 |a ACETYLATION 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ANIMAL MODEL 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a BREAST ADENOCARCINOMA 
690 1 0 |a CELL PROLIFERATION 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DESULFURIZATION 
690 1 0 |a DISSOCIATION CONSTANT 
690 1 0 |a FEMALE 
690 1 0 |a FETAL CALF SERUM 
690 1 0 |a GROWTH INHIBITION 
690 1 0 |a LUNG METASTASIS 
690 1 0 |a MOUSE 
690 1 0 |a NONHUMAN 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a ADENOCARCINOMA 
690 1 0 |a ANALYSIS OF VARIANCE 
690 1 0 |a ANIMAL 
690 1 0 |a ANTINEOPLASTIC AGENTS 
690 1 0 |a BINDING, COMPETITIVE 
690 1 0 |a CELL DIVISION 
690 1 0 |a FEMALE 
690 1 0 |a HEPARIN 
690 1 0 |a MAMMARY NEOPLASMS, EXPERIMENTAL 
690 1 0 |a MICE 
690 1 0 |a MICE, INBRED BALB C 
690 1 0 |a NEOPLASM METASTASIS 
690 1 0 |a RECEPTORS, CELL SURFACE 
690 1 0 |a SUPPORT, NON-U.S. GOV'T 
690 1 0 |a TUMOR CELLS, CULTURED 
690 1 0 |a ANIMALIA 
690 1 0 |a MURINAE 
690 1 0 |a TRITIUM 
700 1 |a de Cidre, L.L. 
700 1 |a de Lustig, E.S. 
700 1 |a Eiján, A.M. 
773 0 |d 1995  |g v. 90  |h pp. 123-131  |k n. 2  |p Cancer Lett.  |x 03043835  |w (AR-BaUEN)CENRE-4108  |t Cancer Letters 
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856 4 0 |u https://doi.org/10.1016/0304-3835(95)03693-Q  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_03043835_v90_n2_p123_Bertolesix  |y Handle 
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999 |c 64681