International journal of hematology · 1997
TEL/AML1 fusion gene resulting from a cryptic t(12;21) is uncommon in adult patients with B-cell lineage ALL and CML lymphoblastic transformation.
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Hoshino K, Asou N, Suzushima H, Osato M, Yamasaki H, Okubo T, Nishimura S, Kiyokawa T, Kawano F, Takatsuki K
Аннотация
TEL is a new member of the ETS-like family on chromosome 12 and forms fusion genes with several partners in leukemia. Among these fusion genes, the TEL/AML1 translocation resulting from t(12;21) is found in approximately one quarter of the childhood B-cell lineage acute lymphoblastic leukemia (ALL) cases and its prognosis is excellent. We examined 42 adult patients with B-cell lineage ALL and 13 adult patients with lymphoblastic transformation of chronic myeloid leukemia (CML) to detect TEL/AML1 fusion genes using the reverse transcriptase-polymerase chain reaction (RT-PCR) and Southern blotting, but no translocation was detected. These findings indicate that absence of the TEL/AML1 fusion transcript partly correlates with the poorer outcome of adult B-cell lineage ALL as compared with childhood ALL and the TEL/AML1 fusion transcript is specific for pediatric B-cell lineage ALL.
Предметные рубрики MeSH
AdolescentAdultAge FactorsAgedAnimalsBiomarkers, TumorBlast CrisisBurkitt LymphomaCell Transformation, NeoplasticChildChromosomes, Human, Pair 12Chromosomes, Human, Pair 21Core Binding Factor Alpha 2 SubunitGene Expression Regulation, LeukemicGene FrequencyHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMiddle AgedNeoplasm ProteinsOncogene Proteins, FusionPrognosisTranslocation, GeneticETS Translocation Variant 6 Protein