id paper:paper_01676806_v45_n3_p211_Chasseing
record_format dspace
spelling paper:paper_01676806_v45_n3_p211_Chasseing2023-06-08T15:16:43Z Bone marrow fibroblastic progenitors in patients with advanced breast cancer Fibroblasts and interleukin-β indometacin interleukin 1beta muramyl dipeptide prostaglandin E2 trypsin adherent cell advanced cancer article bone marrow biopsy bone marrow cell breast cancer cancer staging cell culture cell stimulation clinical article colony forming cell controlled study enzyme linked immunosorbent assay female fibroblast fibroblast culture human human cell mononuclear cell priority journal prostaglandin release stem cell supernatant Biopsy, Needle Bone Marrow Cells Breast Breast Neoplasms Cells, Cultured Dinoprostone Female Fibroblasts Humans Interleukin-1 Stem Cells 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. 1997 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01676806_v45_n3_p211_Chasseing http://hdl.handle.net/20.500.12110/paper_01676806_v45_n3_p211_Chasseing
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Fibroblasts and interleukin-β
indometacin
interleukin 1beta
muramyl dipeptide
prostaglandin E2
trypsin
adherent cell
advanced cancer
article
bone marrow biopsy
bone marrow cell
breast cancer
cancer staging
cell culture
cell stimulation
clinical article
colony forming cell
controlled study
enzyme linked immunosorbent assay
female
fibroblast
fibroblast culture
human
human cell
mononuclear cell
priority journal
prostaglandin release
stem cell
supernatant
Biopsy, Needle
Bone Marrow Cells
Breast
Breast Neoplasms
Cells, Cultured
Dinoprostone
Female
Fibroblasts
Humans
Interleukin-1
Stem Cells
spellingShingle Fibroblasts and interleukin-β
indometacin
interleukin 1beta
muramyl dipeptide
prostaglandin E2
trypsin
adherent cell
advanced cancer
article
bone marrow biopsy
bone marrow cell
breast cancer
cancer staging
cell culture
cell stimulation
clinical article
colony forming cell
controlled study
enzyme linked immunosorbent assay
female
fibroblast
fibroblast culture
human
human cell
mononuclear cell
priority journal
prostaglandin release
stem cell
supernatant
Biopsy, Needle
Bone Marrow Cells
Breast
Breast Neoplasms
Cells, Cultured
Dinoprostone
Female
Fibroblasts
Humans
Interleukin-1
Stem Cells
Bone marrow fibroblastic progenitors in patients with advanced breast cancer
topic_facet Fibroblasts and interleukin-β
indometacin
interleukin 1beta
muramyl dipeptide
prostaglandin E2
trypsin
adherent cell
advanced cancer
article
bone marrow biopsy
bone marrow cell
breast cancer
cancer staging
cell culture
cell stimulation
clinical article
colony forming cell
controlled study
enzyme linked immunosorbent assay
female
fibroblast
fibroblast culture
human
human cell
mononuclear cell
priority journal
prostaglandin release
stem cell
supernatant
Biopsy, Needle
Bone Marrow Cells
Breast
Breast Neoplasms
Cells, Cultured
Dinoprostone
Female
Fibroblasts
Humans
Interleukin-1
Stem Cells
description 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.
title Bone marrow fibroblastic progenitors in patients with advanced breast cancer
title_short Bone marrow fibroblastic progenitors in patients with advanced breast cancer
title_full Bone marrow fibroblastic progenitors in patients with advanced breast cancer
title_fullStr Bone marrow fibroblastic progenitors in patients with advanced breast cancer
title_full_unstemmed Bone marrow fibroblastic progenitors in patients with advanced breast cancer
title_sort bone marrow fibroblastic progenitors in patients with advanced breast cancer
publishDate 1997
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01676806_v45_n3_p211_Chasseing
http://hdl.handle.net/20.500.12110/paper_01676806_v45_n3_p211_Chasseing
_version_ 1768543699232358400