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Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature.
- Source :
-
Scientific reports [Sci Rep] 2017 Sep 11; Vol. 7 (1), pp. 11148. Date of Electronic Publication: 2017 Sep 11. - Publication Year :
- 2017
-
Abstract
- 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.
- Subjects :
- Biomarkers, Tumor
Cell Line, Tumor
DNA-Binding Proteins metabolism
Gene Expression Profiling
Humans
Kaplan-Meier Estimate
Leukemia, Myeloid, Acute pathology
Patient Outcome Assessment
Prognosis
Transcription Factors metabolism
fms-Like Tyrosine Kinase 3 metabolism
DNA-Binding Proteins genetics
Gene Expression Regulation, Leukemic
Karyotype
Leukemia, Myeloid, Acute genetics
Leukemia, Myeloid, Acute mortality
Tandem Repeat Sequences
Transcription Factors genetics
fms-Like Tyrosine Kinase 3 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 28894287
- Full Text :
- https://doi.org/10.1038/s41598-017-11718-8