Asunto(s)
Síndrome de Down/genética , Janus Quinasa 2/genética , Janus Quinasa 3/genética , Leucemia Mieloide/genética , Mutación , Trastornos Mieloproliferativos/genética , Receptores de Trombopoyetina/genética , Niño , Preescolar , Síndrome de Down/complicaciones , Epigénesis Genética , Femenino , Predisposición Genética a la Enfermedad , Humanos , Leucemia Mieloide/etiología , Masculino , Trastornos Mieloproliferativos/etiologíaAsunto(s)
Factor de Transcripción GATA1/genética , Mutación de Línea Germinal , Síndrome de Down/complicaciones , Síndrome de Down/genética , Hematopoyesis/genética , Humanos , Leucemia Megacarioblástica Aguda/etiología , Leucemia Megacarioblástica Aguda/genética , Modelos Biológicos , Isoformas de Proteínas/genéticaAsunto(s)
Proteínas de Unión al ADN/genética , Síndrome de Down/complicaciones , Síndrome de Down/genética , Leucemia Megacarioblástica Aguda/complicaciones , Leucemia Megacarioblástica Aguda/genética , Factores de Transcripción/genética , Factores de Unión al ADN Específico de las Células Eritroides , Factor de Transcripción GATA1 , Humanos , MutaciónRESUMEN
Mutations in transcription factors often contribute to human leukemias by providing a block to normal differentiation. To determine whether mutations in the hematopoietic transcription factor GATA1 are associated with leukemia, we assayed for alterations in the GATA1 gene in bone marrow samples from patients with various subtypes of acute leukemia. Here we summarize our findings that GATA1 is mutated in the leukemic blasts of patients with Down syndrome acute megakaryoblastic leukemia (DS-AMKL). We did not find mutations in GATA1 in leukemic cells of DS patients with other types of acute leukemia, or in other patients with AMKL who did not have DS. Furthermore, we did not detect GATA1 mutations in DNAs from over 75 other patients with acute leukemia or from 21 healthy individuals. Since the GATA1 mutations were restricted to DS-AMKL, we also investigated whether GATA1 was altered in the "preleukemia" of DS, transient myeloproliferative disorder (TMD). TMD is a common myeloid disorder that affects 10% of DS newborns and evolves to AMKL in nearly 30% patients. We detected GATA1 mutations in TMD blasts from every infant examined. Together, these results demonstrate that GATA1 is likely to play a critical role in the etiology of TMD and DS-AMKL, and that mutagenesis of GATA1 represents a very early event in DS myeloid leukemogenesis. We hypothesize that disruption of normal GATA-1 function is an essential step in the initiation of megakaryoblastic leukemia in DS.
Asunto(s)
Proteínas de Unión al ADN/genética , Síndrome de Down/genética , Leucemia Megacarioblástica Aguda/genética , Mutación/genética , Trastornos Mieloproliferativos/genética , Factores de Transcripción/genética , Médula Ósea/patología , Análisis Mutacional de ADN , Proteínas de Unión al ADN/metabolismo , Progresión de la Enfermedad , Síndrome de Down/complicaciones , Factores de Unión al ADN Específico de las Células Eritroides , Factor de Transcripción GATA1 , Humanos , Leucemia Megacarioblástica Aguda/complicaciones , Trastornos Mieloproliferativos/complicaciones , Factores de Transcripción/metabolismoRESUMEN
As many as 10% of infants with Down syndrome (DS) present with transient myeloproliferative disorder (TMD) at or shortly after birth. TMD is characterized by an abundance of blasts within the peripheral blood and liver, and notably undergoes spontaneous remission in the majority of cases. TMD may be a precursor to acute megakaryoblastic leukemia (AMKL), with an estimated 30% of TMD patients developing AMKL within 3 years. We recently reported that mutations in the transcription factor GATA1 are associated with DS-AMKL. To determine whether the acquisition of GATA1 mutations is a late event restricted to acute leukemia, we analyzed GATA1 in DNA from TMD patients. Here we report that GATA1 is mutated in the TMD blasts from every infant examined. These results demonstrate that GATA1 is likely to play a critical role in the etiology of TMD, and mutagenesis of GATA1 represents a very early event in DS myeloid leukemogenesis.