Bone marrow fibroblastic progenitors in patients with advanced breast cancer

Bone marrow fibroblast colony-forming cells (CFU-F) were studied in fifteen consecutive untreated breast cancer patients (BCP) with clinical stages III and IV, and in sixteen normal controls (NC). A decreased number of CFU-F was observed in BCP compared to NC (p < 0.004). Confluence of the ad...

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Autor principal: Chasseing, N.A
Otros Autores: Trejo, Y.G, Bordenave, R.H, Bullorsky, E.O, Diaz, N.B, Rumi, L.S
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1997
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
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024 7 |2 cas  |a indometacin, 53-86-1, 74252-25-8, 7681-54-1; prostaglandin E2, 363-24-6; trypsin, 9002-07-7; Dinoprostone, 363-24-6; Interleukin-1 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a BCTRD 
100 1 |a Chasseing, N.A. 
245 1 0 |a Bone marrow fibroblastic progenitors in patients with advanced breast cancer 
260 |c 1997 
270 1 0 |m Chasseing, N.A.; Inst. Biologia Medicina Experimental, Obligado 2490, 1428 Buenos Aires, Argentina 
506 |2 openaire  |e Política editorial 
504 |a Tavassoli, M., Hardy, C.L., Molecular basis of homing of intravenously transplanted stem cells to the marrow (1990) Blood, 76, pp. 1059-1070 
504 |a Mayani, H., Guilbert, L.J., Janowska-Wieczorek, A., Biology of hemopoietic microenvironment (1992) Eur J Haematol, 49, pp. 225-233 
504 |a Andreoni, C., Moreau, I., Rigal, D., Long-term culture of human bone marrow (1990) I. Characterization of Adherent Cells in Flow Cytometry. Exp Hematol, 18, pp. 431-437 
504 |a Bentley, S.A., The role and composition of the adherent layer in long-term bone marrow culture (1984) Long-term Bone Marrow Culture, pp. 141-156. , Wright DG, Greenberger J (eds) Alan R Liss Inc, New York 
504 |a Greenberger, J.S., The hemopoietic microenvironment (1991) Crit Rev Oncol Hematol, 11, pp. 65-84 
504 |a Castro Malaspina, H., Ebbel, W., Wang, S.Y., Human bone marrow fibroblast colony forming units (CFU-F) (1984) Myelofibrosis and the Biology of Connective Tissue, pp. 209-236. , Berk PD, Castro Malaspina H, Wasserman LR (eds) Alan R Liss Inc, New York 
504 |a Friedenstein, A.J., Chailakhyan, R.K., Latsinik, N.V., Panasyuk, A.F., Keiliss-Borok, I.V., Stromal cells responsible for transferring the microenvironment of the hematopoietic tissue (1974) Transplantation, 17, pp. 331-340 
504 |a Castro Malaspina, H., Gay, R.E., Resnick, G., Kapoor, N., Meyers, P., Chiarieri, D., McKenzie, S., Moore, M.A.S., Characterization of human bone marrow fibroblast colony-forming cells (CFU-F) and their progeny (1980) Blood, 56, pp. 289-301 
504 |a Croizat, H., Eskinazi, D., Axelrad, A.A., Stromal cell colonies produced by non-adherent cells from long term human bone marrow cultures enhance erythropoietic burst formation (1986) Exp Hematol, 14, pp. 324-326 
504 |a Clarke, E., McCann, S.R., Stromal colonies can be grown from the non-adherent cells in human long term bone marrow cultures (1991) Eur J Haematol, 46, pp. 296-300 
504 |a Tsai, S., Patel, V., Beaumont, E., Lodish, H.F., Nathan, D.G., Sieff, C.A., Differential binding of erythroid and myeloid progenitors to fibroblasts and fibronectin (1987) Blood, 69, pp. 1587-1594 
504 |a Moreau, I., Andreoni, C., Caux, C., Saeland, S., Rigal, D., Modification of human long-term bone marrow cultures: Establishment of a functional stromal microenvironment devoid of myeloid progenitors (1992) Eur J Haematol, 49, pp. 29-35 
504 |a Kovacs, E.J., Fibrogenic cytokines: The role of immune mediators in the development of scar tissue (1991) Immunol Today, 12, pp. 17-23 
504 |a Ershler, W.B., Ross, J., Finlay, J.L., Shahidi, N.T., Bone marrow microenvironment defect in congenital hypoplastic anemia (1980) N Engl J Med, 302, pp. 1321-1327 
504 |a Hirala, J., Katsuno, M., Kaneko, S., Clinical significance of human bone marrow stromal cell colonies in acute leukemias (1986) Leuk Res, 12, pp. 1441-1445 
504 |a Takahashi, M., Keating, A., Singer, J.W., A functional defect in irradiated adherent layers from chronic myelogenous leukemia long-term marrow cultures (1985) Exp Hematol, 13, pp. 926-931 
504 |a Coutinho, L.H., Geary, C.G., Chang, J., Harrison, C., Testa, N.G., Functional studies of bone marrow haematopoietic and stroma cells in the myelodysplastic syndrome (MDS) (1990) British J Haematol, 75, pp. 16-25 
504 |a Testa, N.G., Hendry, J.H., Molineux, G., Long term hone marrow damage in experimental systems and in patients after radiation or chemotherapy (1985) Anti Cancer Res, 5, p. 101 
504 |a Knospe, W.H., Long term bone marrow damage after irradiation (1988) Hematopoiesis: Long Term Effects of Chemotherapy and Radiation, pp. 93-130. , Testa NG, Gale RP (eds) Marcel Dekker Inc 
504 |a Pike, B.L., Robinson, W.A., Human bone marrow colony growth in agar-gel (1970) J Cell Physiol, 76, pp. 77-84 
504 |a Welte, K., Platzer, E., Lu, L., Gabrilove, J., Levi, E., Mertelsman, R., Moore, M.A.S., Purification and biochemical characterization of human pluripotent hematopoietic colony stimulating factor (1985) Proc Natl Acad Sci USA, 82, pp. 1526-1530 
504 |a Eaves, A.C., Eaves, C.J., Maintenance and proliferation control of primitive hemopoietic progenitors in long-term cultures of marrow cells (1988) Blood Cells, 14, pp. 355-368 
504 |a Juneja, H.S., Gardner, F.H., Minguell, J.J., Helmer, R.E., Abnormal marrow fibroblasts in aplastic anemia (1984) Exp Hematol, 12, pp. 221-230 
504 |a Korn, J.H., Halushka, P.V., Leroy, E.C., Mononuclear cell modulation of connective tissue function. Suppression of fibroblast growth by stimulation of endogenous prostaglandin production (1980) J Clin Invest, 65, pp. 543-554 
504 |a Freundlich, B., Bomalaski, J.S., Neilson, E., Jimenez, S.A., Regulation of fibroblast proliferation and collagen synthesis by cytokines (1986) Immunol Today, 7, pp. 303-307 
504 |a Paulsson, Y., Hammacher, A., Heldin, C., Westermark, B., Possible autocrine feed-back in the prereplicative phase of human fibroblasts (1987) Nature, 328, pp. 715-717 
504 |a Lin, J.X., Vilcek, J., Tumor necrosis factor and interleukin-1 cause a rapid and transient stimulation of c-fos and c-myc mRNA levels in human fibroblasts (1987) J Biol Chem, 262, pp. 11908-11911 
520 3 |a Bone marrow fibroblast colony-forming cells (CFU-F) were studied in fifteen consecutive untreated breast cancer patients (BCP) with clinical stages III and IV, and in sixteen normal controls (NC). A decreased number of CFU-F was observed in BCP compared to NC (p < 0.004). Confluence of the adherent cell layer was observed in all normal bone marrow mononuclear cells (MC) cultures, while a lower proportion of cultures from BCP (11/15) showed confluent adherent cell layers. When MC cultures of BCP were treated with indomethacin (Indo, 10 -6 M) 50% of them increased the number of CFU-F compared to the value obtained without treatment. In addition, a significant increase in the release of PGE2 in BCP cultures was observed before Indo treatment. Moreover, after MC were fractionated into adherent and non-adherent progenitors, the CFU-F decreased in both types of fractions of BCP compared to NC value (p < 0.02 and < 0.05, respectively). The number of light density MC per 10 ml of bone marrow aspirate and the number of trypsin-sensitive adherent progenitors were lower than NC in BCP (p < 0.02 and 0.013, respectively). Total MC and fibroblasts (fourth passage) were cultivated to evaluate the production of interleukin-1β (IL-1β) by ELISA methodology. Results indicated no difference of IL-1β spontaneous release when total MC cultures of both groups were compared. However, the levels of this cytokine were lower (< 10 pg/ml) in fibroblast culture supernatants of BCP compared to NC (1217 ± 74 pg/ml). Fibroblast cultures from BCP showed low or no release of IL-1β after muramyl-dipeptide (MDP, 1 μg/ml) stimulation. In conclusion, the defective proliferative and confluence capacity of BCP fibroblastic progenitors may be related to the decrease in the production of IL-1β by these precursors.  |l eng 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: 1Research Member of the Consejo Nacional de Investigaciones Cientificas y Técnicas de la República Argentina (CONICET); 2Instituto de Biología Medicina Experimental, Obligado 2490, 1428 Buenos Aires, Argentina; 3Deparment of Oncology, Hospital Zonal de Agudos I. Iriarte, Quilmes, Pcia. de Buenos Aires, Argentina; 4Department of Hematology and Bone Marrow Transplantation, Hospital Británico, Buenos Aires, Argentina; 5Hematology Division, Department of Clinical Biochemistry, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Argentina 
536 |a Detalles de la financiación: We are grateful to the personnel of the Department of Oncology from Hospital Zonal de Agudos I. Iriarte for assistance with the patients. This study was supported by the Research Council of Argentina (Consejo Nacional de Investigaciones Científi-cas y Técnicas de la Argentina, CONICET). 
593 |a Consejo Nac. de Invest. Cie. y T., Argentina 
593 |a Inst. de Biol. Medicina Experimental, Obligado 2490, 1428 Buenos Aires, Argentina 
593 |a Deparment of Oncology, Hospital Zonal de Agudos I. Iriarte, Quilmes, Pcia. de Buenos Aires, Argentina 
593 |a Department of Hematology, Hospital Británico, Buenos Aires, Argentina 
593 |a Hematology Division, Department of Clinical Biochemistry, Universidad de Buenos Aires, Argentina 
593 |a Inst. de Biol. y Med. Experimental, Obligado 2490, 1428 Buenos Aires, Argentina 
690 1 0 |a FIBROBLASTS AND INTERLEUKIN-Β 
690 1 0 |a INDOMETACIN 
690 1 0 |a INTERLEUKIN 1BETA 
690 1 0 |a MURAMYL DIPEPTIDE 
690 1 0 |a PROSTAGLANDIN E2 
690 1 0 |a TRYPSIN 
690 1 0 |a ADHERENT CELL 
690 1 0 |a ADVANCED CANCER 
690 1 0 |a ARTICLE 
690 1 0 |a BONE MARROW BIOPSY 
690 1 0 |a BONE MARROW CELL 
690 1 0 |a BREAST CANCER 
690 1 0 |a CANCER STAGING 
690 1 0 |a CELL CULTURE 
690 1 0 |a CELL STIMULATION 
690 1 0 |a CLINICAL ARTICLE 
690 1 0 |a COLONY FORMING CELL 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a ENZYME LINKED IMMUNOSORBENT ASSAY 
690 1 0 |a FEMALE 
690 1 0 |a FIBROBLAST 
690 1 0 |a FIBROBLAST CULTURE 
690 1 0 |a HUMAN 
690 1 0 |a HUMAN CELL 
690 1 0 |a MONONUCLEAR CELL 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a PROSTAGLANDIN RELEASE 
690 1 0 |a STEM CELL 
690 1 0 |a SUPERNATANT 
690 1 0 |a BIOPSY, NEEDLE 
690 1 0 |a BONE MARROW CELLS 
690 1 0 |a BREAST 
690 1 0 |a BREAST NEOPLASMS 
690 1 0 |a CELLS, CULTURED 
690 1 0 |a DINOPROSTONE 
690 1 0 |a FEMALE 
690 1 0 |a FIBROBLASTS 
690 1 0 |a HUMANS 
690 1 0 |a INTERLEUKIN-1 
690 1 0 |a STEM CELLS 
700 1 |a Trejo, Y.G. 
700 1 |a Bordenave, R.H. 
700 1 |a Bullorsky, E.O. 
700 1 |a Diaz, N.B. 
700 1 |a Rumi, L.S. 
773 0 |d 1997  |g v. 45  |h pp. 211-218  |k n. 3  |p BREAST CANCER RES. TREAT.  |x 01676806  |t Breast Cancer Research and Treatment 
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