Regulation of the bone marrow microenvironment by G-CSF: Effects of G-CSF on acute lymphoblastic leukaemia.

It has been suggested that disruption of the lymphoid niche by G-CSF may be of therapeutic benefit to patients with acute lymphoblastic leukaemia. We used a xenograft model to determine the effect of G-CSF on ALL progression in a minimal residual disease setting. Consistent with the effects on norma...

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Main Authors: Jordan Basnett, Vicki Xie, Adam Cisterne, Ken Bradstock, Linda Bendall
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5690634?pdf=render
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author Jordan Basnett
Vicki Xie
Adam Cisterne
Ken Bradstock
Linda Bendall
author_facet Jordan Basnett
Vicki Xie
Adam Cisterne
Ken Bradstock
Linda Bendall
author_sort Jordan Basnett
collection DOAJ
description It has been suggested that disruption of the lymphoid niche by G-CSF may be of therapeutic benefit to patients with acute lymphoblastic leukaemia. We used a xenograft model to determine the effect of G-CSF on ALL progression in a minimal residual disease setting. Consistent with the effects on normal murine B cell progenitors, G-CSF slowed disease in the majority of ALL xenografts tested, suggesting that G-CSF may provide benefits beyond neutrophil recovery for ALL patients. However, two of eight xenografts demonstrated accelerated disease progression. G-CSF could be detrimental for these patients due to expansion of the malignant clone.
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spelling doaj.art-2291e7cba0334cd5abfcebea6a64563f2022-12-22T02:06:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011211e018804210.1371/journal.pone.0188042Regulation of the bone marrow microenvironment by G-CSF: Effects of G-CSF on acute lymphoblastic leukaemia.Jordan BasnettVicki XieAdam CisterneKen BradstockLinda BendallIt has been suggested that disruption of the lymphoid niche by G-CSF may be of therapeutic benefit to patients with acute lymphoblastic leukaemia. We used a xenograft model to determine the effect of G-CSF on ALL progression in a minimal residual disease setting. Consistent with the effects on normal murine B cell progenitors, G-CSF slowed disease in the majority of ALL xenografts tested, suggesting that G-CSF may provide benefits beyond neutrophil recovery for ALL patients. However, two of eight xenografts demonstrated accelerated disease progression. G-CSF could be detrimental for these patients due to expansion of the malignant clone.http://europepmc.org/articles/PMC5690634?pdf=render
spellingShingle Jordan Basnett
Vicki Xie
Adam Cisterne
Ken Bradstock
Linda Bendall
Regulation of the bone marrow microenvironment by G-CSF: Effects of G-CSF on acute lymphoblastic leukaemia.
PLoS ONE
title Regulation of the bone marrow microenvironment by G-CSF: Effects of G-CSF on acute lymphoblastic leukaemia.
title_full Regulation of the bone marrow microenvironment by G-CSF: Effects of G-CSF on acute lymphoblastic leukaemia.
title_fullStr Regulation of the bone marrow microenvironment by G-CSF: Effects of G-CSF on acute lymphoblastic leukaemia.
title_full_unstemmed Regulation of the bone marrow microenvironment by G-CSF: Effects of G-CSF on acute lymphoblastic leukaemia.
title_short Regulation of the bone marrow microenvironment by G-CSF: Effects of G-CSF on acute lymphoblastic leukaemia.
title_sort regulation of the bone marrow microenvironment by g csf effects of g csf on acute lymphoblastic leukaemia
url http://europepmc.org/articles/PMC5690634?pdf=render
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