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http://purl.uniprot.org/citations/20678218http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20678218http://www.w3.org/2000/01/rdf-schema#comment"

Background

Gene mutation is an important mechanism of myeloid leukemogenesis. However, the number and combination of gene mutated in myeloid malignancies is still a matter of investigation.

Methods

We searched for mutations in the ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in 65 myelodysplastic syndromes (MDSs) and 64 acute myeloid leukemias (AMLs) without balanced translocation or complex karyotype.

Results

Mutations in ASXL1 and CBL were frequent in refractory anemia with excess of blasts. Mutations in TET2 occurred with similar frequency in MDSs and AMLs and associated equally with either ASXL1 or NPM1 mutations. Mutations of RUNX1 were mutually exclusive with TET2 and combined with ASXL1 but not with NPM1. Mutations in FLT3 (mutation and internal tandem duplication), IDH1, IDH2, NPM1 and WT1 occurred primarily in AMLs.

Conclusion

Only 14% MDSs but half AMLs had at least two mutations in the genes studied. Based on the observed combinations and exclusions we classified the 12 genes into four classes and propose a highly speculative model that at least a mutation in one of each class is necessary for developing AML with simple or normal karyotype."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.org/dc/terms/identifier"doi:10.1186/1471-2407-10-401"xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Olschwang S."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Birnbaum D."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Carbuccia N."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Gelsi-Boyer V."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Mozziconacci M.J."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Nezri M."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Trouplin V."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Vey N."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Raynaud S."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Murati A."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Rocquain J."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/author"Tadrist Z."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/name"BMC Cancer"xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/pages"401"xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/title"Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias."xsd:string
http://purl.uniprot.org/citations/20678218http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/20678218http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/20678218
http://purl.uniprot.org/citations/20678218http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/20678218
http://purl.uniprot.org/uniprot/#_A0A140VJQ2-mappedCitation-20678218http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/20678218
http://purl.uniprot.org/uniprot/#_A0A024R3Y6-mappedCitation-20678218http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/20678218
http://purl.uniprot.org/uniprot/#_A0A221ZRZ1-mappedCitation-20678218http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/20678218
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