Source:http://linkedlifedata.com/resource/pubmed/id/17008890
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2006-10-25
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pubmed:abstractText |
Activating mutations in NOTCH1 are found in over 50% of human T-cell lymphoblastic leukemias (T-ALLs). Here, we report the analysis for activating NOTCH1 mutations in a large number of acute myeloid leukemia (AML) primary samples and cell lines. We found activating mutations in NOTCH1 in a single M0 primary AML sample, in three (ML1, ML2 and CTV-1) out of 23 AML cell lines and in the diagnostic (myeloid) and relapsed (T-lymphoid) clones in a patient with lineage switch leukemia. Importantly, the ML1 and ML2 AML cell lines are derived from an AML relapse in a patient initially diagnosed with T-ALL. Overall, these results demonstrate that activating mutations in NOTCH1 are mostly restricted to T-ALL and are rare in AMLs. The presence of NOTCH1 mutations in myeloid and T-lymphoid clones in lineage switch leukemias establishes the common clonal origin of the diagnostic and relapse blast populations and suggests a stem cell origin of NOTCH1 mutations during the molecular pathogenesis of these tumors.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0887-6924
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pubmed:author |
pubmed-author:AsterJ CJC,
pubmed-author:CaligiuriM AMA,
pubmed-author:FerrandoA AAA,
pubmed-author:FoxE AEA,
pubmed-author:GalinskyII,
pubmed-author:KalmantiMM,
pubmed-author:LookA TAT,
pubmed-author:McKennaKK,
pubmed-author:O-NeilJJ,
pubmed-author:PalomeroTT,
pubmed-author:StiakakiEE,
pubmed-author:StoneRR,
pubmed-author:SuzukawaKK
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pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1963-6
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pubmed:dateRevised |
2007-12-3
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pubmed:meshHeading |
pubmed-meshheading:17008890-Acute Disease,
pubmed-meshheading:17008890-Base Sequence,
pubmed-meshheading:17008890-Cell Line, Tumor,
pubmed-meshheading:17008890-Cell Lineage,
pubmed-meshheading:17008890-Gene Deletion,
pubmed-meshheading:17008890-Gene Expression Regulation, Leukemic,
pubmed-meshheading:17008890-Hematopoietic Stem Cells,
pubmed-meshheading:17008890-Humans,
pubmed-meshheading:17008890-Leukemia, Myeloid,
pubmed-meshheading:17008890-Point Mutation,
pubmed-meshheading:17008890-Receptor, Notch1,
pubmed-meshheading:17008890-Recurrence,
pubmed-meshheading:17008890-T-Lymphocytes
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pubmed:year |
2006
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pubmed:articleTitle |
Activating mutations in NOTCH1 in acute myeloid leukemia and lineage switch leukemias.
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pubmed:affiliation |
Institute for Cancer Genetics, Columbia University, New York, NY 10032, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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