Abstract
In this issue of Cell Stem Cell, Somervaille et al. (2009) have demonstrated convincingly that reversion to an embryonic transcriptional program through defective MLL gene expression contributes to the generation of myeloid leukemia stem cells.
MeSH terms
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Animals
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Cellular Reprogramming
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Gene Expression Regulation, Developmental*
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Histone-Lysine N-Methyltransferase
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Humans
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Leukemia, Myeloid, Acute / pathology
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Leukemia, Myeloid, Acute / physiopathology
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Myeloid-Lymphoid Leukemia Protein / genetics
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Myeloid-Lymphoid Leukemia Protein / metabolism*
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Neoplastic Stem Cells / physiology*
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Transcription, Genetic*
Substances
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KMT2A protein, human
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Myeloid-Lymphoid Leukemia Protein
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Histone-Lysine N-Methyltransferase