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Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature
Growth Factor Independence 1 (GFI1) is a transcriptional repressor that plays a critical role during both myeloid and lymphoid haematopoietic lineage commitment. Several studies have demonstrated the involvement of GFI1 in haematological malignancies and have suggested that low expression of GFI1 is...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593973/ https://www.ncbi.nlm.nih.gov/pubmed/28894287 http://dx.doi.org/10.1038/s41598-017-11718-8 |
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author | Volpe, Giacomo Walton, David S. Grainger, David E. Ward, Carl Cauchy, Pierre Blakemore, Daniel Coleman, Daniel J. L. Cockerill, Peter N. Garcia, Paloma Frampton, Jon |
author_facet | Volpe, Giacomo Walton, David S. Grainger, David E. Ward, Carl Cauchy, Pierre Blakemore, Daniel Coleman, Daniel J. L. Cockerill, Peter N. Garcia, Paloma Frampton, Jon |
author_sort | Volpe, Giacomo |
collection | PubMed |
description | Growth Factor Independence 1 (GFI1) is a transcriptional repressor that plays a critical role during both myeloid and lymphoid haematopoietic lineage commitment. Several studies have demonstrated the involvement of GFI1 in haematological malignancies and have suggested that low expression of GFI1 is a negative indicator of disease progression for both myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML). In this study, we have stratified AML patients into those defined as having a normal karyotype (CN-AML). Unlike the overall pattern in AML, those patients with CN-AML have a poorer survival rate when GFI1 expression is high. In this group, high GFI1 expression is paralleled by higher FLT3 expression, and, even when the FLT3 gene is not mutated, exhibit a FLT3-ITD signature of gene expression. Knock-down of GFI1 expression in the human AML Fujioka cell line led to a decrease in the level of FLT3 RNA and protein and to the down regulation of FLT3-ITD signature genes, thus linking two major prognostic indicators for AML. |
format | Online Article Text |
id | pubmed-5593973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55939732017-09-13 Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature Volpe, Giacomo Walton, David S. Grainger, David E. Ward, Carl Cauchy, Pierre Blakemore, Daniel Coleman, Daniel J. L. Cockerill, Peter N. Garcia, Paloma Frampton, Jon Sci Rep Article Growth Factor Independence 1 (GFI1) is a transcriptional repressor that plays a critical role during both myeloid and lymphoid haematopoietic lineage commitment. Several studies have demonstrated the involvement of GFI1 in haematological malignancies and have suggested that low expression of GFI1 is a negative indicator of disease progression for both myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML). In this study, we have stratified AML patients into those defined as having a normal karyotype (CN-AML). Unlike the overall pattern in AML, those patients with CN-AML have a poorer survival rate when GFI1 expression is high. In this group, high GFI1 expression is paralleled by higher FLT3 expression, and, even when the FLT3 gene is not mutated, exhibit a FLT3-ITD signature of gene expression. Knock-down of GFI1 expression in the human AML Fujioka cell line led to a decrease in the level of FLT3 RNA and protein and to the down regulation of FLT3-ITD signature genes, thus linking two major prognostic indicators for AML. Nature Publishing Group UK 2017-09-11 /pmc/articles/PMC5593973/ /pubmed/28894287 http://dx.doi.org/10.1038/s41598-017-11718-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Volpe, Giacomo Walton, David S. Grainger, David E. Ward, Carl Cauchy, Pierre Blakemore, Daniel Coleman, Daniel J. L. Cockerill, Peter N. Garcia, Paloma Frampton, Jon Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature |
title | Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature |
title_full | Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature |
title_fullStr | Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature |
title_full_unstemmed | Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature |
title_short | Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature |
title_sort | prognostic significance of high gfi1 expression in aml of normal karyotype and its association with a flt3-itd signature |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593973/ https://www.ncbi.nlm.nih.gov/pubmed/28894287 http://dx.doi.org/10.1038/s41598-017-11718-8 |
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