Bone marrow fibroblasts in patients with advanced lung cancer

In a previous study we demonstrated that the incidence of fibroblast colony-forming units (CFU-F) was very low in bone marrow primary cultures from the majority of untreated advanced non-small lung cancer patients (LCP) compared to normal controls (NC). For this reason, we studied the ability of bone marrow stromal cells to achieve confluence in primary cultures and their proliferative capacity following four continuous subcultures in consecutive untreated LCP and NC. We also evaluated the production of interleukin-1ß (IL-1ß) and prostaglandin E2 (PGE2) by pure fibroblasts. Bone marrow was obtained from 20 LCP and 20 NC. A CFU-F assay was used to investigate the proliferative and confluence capacity. Levels of IL-1ß and PGE2 in conditioned medium (CM) of pure fibroblast cultures were measured with an ELISA kit and RIA kit, respectively. Only fibroblasts from 6/13 (46%) LCP confluent primary cultures had the capacity to proliferate following four subcultures (NC = 100%). Levels of spontaneously released IL-1ß were below 10 pg/ml in the CM of LCP, while NC had a mean value of 1,217 ± 74 pg/ml. In contrast, levels of PGE2 in these CM of LCP were higher (77.5 ± 23.6 pg/ml) compared to NC (18.5 ± 0.9 pg/ml). In conclusion, bone marrow fibroblasts from LCP presented a defective proliferative and confluence capacity, and this deficiency may be associated with the alteration of IL-1ß and PGE2 production.

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Main Authors: Chasseing,N.A., Hofer,E., Bordenave,R.H., Shanley,C., Rumi,L.S.
Format: Digital revista
Language:English
Published: Associação Brasileira de Divulgação Científica 2001
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2001001100014
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spelling oai:scielo:S0100-879X20010011000142001-11-07Bone marrow fibroblasts in patients with advanced lung cancerChasseing,N.A.Hofer,E.Bordenave,R.H.Shanley,C.Rumi,L.S. fibroblasts interleukin-1 prostaglandin E2 cancer In a previous study we demonstrated that the incidence of fibroblast colony-forming units (CFU-F) was very low in bone marrow primary cultures from the majority of untreated advanced non-small lung cancer patients (LCP) compared to normal controls (NC). For this reason, we studied the ability of bone marrow stromal cells to achieve confluence in primary cultures and their proliferative capacity following four continuous subcultures in consecutive untreated LCP and NC. We also evaluated the production of interleukin-1ß (IL-1ß) and prostaglandin E2 (PGE2) by pure fibroblasts. Bone marrow was obtained from 20 LCP and 20 NC. A CFU-F assay was used to investigate the proliferative and confluence capacity. Levels of IL-1ß and PGE2 in conditioned medium (CM) of pure fibroblast cultures were measured with an ELISA kit and RIA kit, respectively. Only fibroblasts from 6/13 (46%) LCP confluent primary cultures had the capacity to proliferate following four subcultures (NC = 100%). Levels of spontaneously released IL-1ß were below 10 pg/ml in the CM of LCP, while NC had a mean value of 1,217 ± 74 pg/ml. In contrast, levels of PGE2 in these CM of LCP were higher (77.5 ± 23.6 pg/ml) compared to NC (18.5 ± 0.9 pg/ml). In conclusion, bone marrow fibroblasts from LCP presented a defective proliferative and confluence capacity, and this deficiency may be associated with the alteration of IL-1ß and PGE2 production.info:eu-repo/semantics/openAccessAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research v.34 n.11 20012001-11-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2001001100014en10.1590/S0100-879X2001001100014
institution SCIELO
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country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
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region America del Sur
libraryname SciELO
language English
format Digital
author Chasseing,N.A.
Hofer,E.
Bordenave,R.H.
Shanley,C.
Rumi,L.S.
spellingShingle Chasseing,N.A.
Hofer,E.
Bordenave,R.H.
Shanley,C.
Rumi,L.S.
Bone marrow fibroblasts in patients with advanced lung cancer
author_facet Chasseing,N.A.
Hofer,E.
Bordenave,R.H.
Shanley,C.
Rumi,L.S.
author_sort Chasseing,N.A.
title Bone marrow fibroblasts in patients with advanced lung cancer
title_short Bone marrow fibroblasts in patients with advanced lung cancer
title_full Bone marrow fibroblasts in patients with advanced lung cancer
title_fullStr Bone marrow fibroblasts in patients with advanced lung cancer
title_full_unstemmed Bone marrow fibroblasts in patients with advanced lung cancer
title_sort bone marrow fibroblasts in patients with advanced lung cancer
description In a previous study we demonstrated that the incidence of fibroblast colony-forming units (CFU-F) was very low in bone marrow primary cultures from the majority of untreated advanced non-small lung cancer patients (LCP) compared to normal controls (NC). For this reason, we studied the ability of bone marrow stromal cells to achieve confluence in primary cultures and their proliferative capacity following four continuous subcultures in consecutive untreated LCP and NC. We also evaluated the production of interleukin-1ß (IL-1ß) and prostaglandin E2 (PGE2) by pure fibroblasts. Bone marrow was obtained from 20 LCP and 20 NC. A CFU-F assay was used to investigate the proliferative and confluence capacity. Levels of IL-1ß and PGE2 in conditioned medium (CM) of pure fibroblast cultures were measured with an ELISA kit and RIA kit, respectively. Only fibroblasts from 6/13 (46%) LCP confluent primary cultures had the capacity to proliferate following four subcultures (NC = 100%). Levels of spontaneously released IL-1ß were below 10 pg/ml in the CM of LCP, while NC had a mean value of 1,217 ± 74 pg/ml. In contrast, levels of PGE2 in these CM of LCP were higher (77.5 ± 23.6 pg/ml) compared to NC (18.5 ± 0.9 pg/ml). In conclusion, bone marrow fibroblasts from LCP presented a defective proliferative and confluence capacity, and this deficiency may be associated with the alteration of IL-1ß and PGE2 production.
publisher Associação Brasileira de Divulgação Científica
publishDate 2001
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2001001100014
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AT hofere bonemarrowfibroblastsinpatientswithadvancedlungcancer
AT bordenaverh bonemarrowfibroblastsinpatientswithadvancedlungcancer
AT shanleyc bonemarrowfibroblastsinpatientswithadvancedlungcancer
AT rumils bonemarrowfibroblastsinpatientswithadvancedlungcancer
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