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Abstract:

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.

Registro:

Documento: Artículo
Título:Heparin receptors in two murine mammary adenocarcinomas with different metastatic ability: relationship with growth inhibition
Autor:Bertolesix, G.E.; de Cidre, L.L.; de Lustig, E.S.; Eiján, A.M.
Filiación:Area Investigación, Institute de Oncologia A.H. Roffo, Universidad de Buenos Aires, Av. San Martín 5481, Buenos Aires, 1417, Argentina
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
Palabras clave:Growth inhibition; Heparin; Metastasis; Receptor; Tumor; heparin; membrane receptor; tritium; acetylation; animal cell; animal experiment; animal model; animal tissue; article; breast adenocarcinoma; cell proliferation; controlled study; desulfurization; dissociation constant; female; fetal calf serum; growth inhibition; lung metastasis; mouse; nonhuman; priority journal; Adenocarcinoma; Analysis of Variance; Animal; Antineoplastic Agents; Binding, Competitive; Cell Division; Female; Heparin; Mammary Neoplasms, Experimental; Mice; Mice, Inbred BALB C; Neoplasm Metastasis; Receptors, Cell Surface; Support, Non-U.S. Gov't; Tumor Cells, Cultured; Animalia; Murinae; Tritium
Año:1995
Volumen:90
Número:2
Página de inicio:123
Página de fin:131
DOI: http://dx.doi.org/10.1016/0304-3835(95)03693-Q
Título revista:Cancer Letters
Título revista abreviado:Cancer Lett.
ISSN:03043835
CODEN:CALED
CAS:Antineoplastic Agents; heparin receptor; Heparin, 9005-49-6; Receptors, Cell Surface
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03043835_v90_n2_p123_Bertolesix

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Citas:

---------- APA ----------
Bertolesix, G.E., de Cidre, L.L., de Lustig, E.S. & Eiján, A.M. (1995) . Heparin receptors in two murine mammary adenocarcinomas with different metastatic ability: relationship with growth inhibition. Cancer Letters, 90(2), 123-131.
http://dx.doi.org/10.1016/0304-3835(95)03693-Q
---------- CHICAGO ----------
Bertolesix, G.E., de Cidre, L.L., de Lustig, E.S., Eiján, A.M. "Heparin receptors in two murine mammary adenocarcinomas with different metastatic ability: relationship with growth inhibition" . Cancer Letters 90, no. 2 (1995) : 123-131.
http://dx.doi.org/10.1016/0304-3835(95)03693-Q
---------- MLA ----------
Bertolesix, G.E., de Cidre, L.L., de Lustig, E.S., Eiján, A.M. "Heparin receptors in two murine mammary adenocarcinomas with different metastatic ability: relationship with growth inhibition" . Cancer Letters, vol. 90, no. 2, 1995, pp. 123-131.
http://dx.doi.org/10.1016/0304-3835(95)03693-Q
---------- VANCOUVER ----------
Bertolesix, G.E., de Cidre, L.L., de Lustig, E.S., Eiján, A.M. Heparin receptors in two murine mammary adenocarcinomas with different metastatic ability: relationship with growth inhibition. Cancer Lett. 1995;90(2):123-131.
http://dx.doi.org/10.1016/0304-3835(95)03693-Q