Abstract
Tumor-associated chromosome translocations usually lead to the formation of two reciprocal fusion genes: one thought to be involved in the transformation process, the other the mechanical consequence of the translocation event. In the case of acute promyelocytic leukemia (APL) blasts, the 15;17 chromosome translocation generates the putatively transforming PML/RARa fusion gene and its reciprocal RARa/PML. We report APL cases with submicroscopic 15;17 recombinations leading to the formation of nonreciprocal PML/RARa or RARa/PML fusion genes. Therefore, each of the two reciprocal translocation products may be independently formed and selected by the leukemic phenotype, implying that both are involved in tumorigenesis.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Base Sequence
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Chromosomes, Human, Pair 15 / ultrastructure*
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Chromosomes, Human, Pair 17 / ultrastructure*
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DNA, Neoplasm / genetics
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Female
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Humans
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In Situ Hybridization, Fluorescence
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Leukemia, Promyelocytic, Acute / genetics*
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Male
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Molecular Sequence Data
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Neoplasm Proteins / genetics*
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Neoplasm Proteins / physiology
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Nuclear Proteins*
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Oncogene Proteins, Fusion / genetics*
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Oncogene Proteins, Fusion / physiology
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Promyelocytic Leukemia Protein
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Receptors, Retinoic Acid / genetics*
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Retinoic Acid Receptor alpha
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Transcription Factors / genetics*
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Translocation, Genetic*
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Tumor Suppressor Proteins
Substances
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DNA, Neoplasm
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Neoplasm Proteins
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Nuclear Proteins
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Oncogene Proteins, Fusion
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Promyelocytic Leukemia Protein
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RARA protein, human
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Receptors, Retinoic Acid
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Retinoic Acid Receptor alpha
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Transcription Factors
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Tumor Suppressor Proteins
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PML protein, human