Publication: New hPSC-based human models to study pediatric Acute Megakaryoblastic Leukemia harboring the fusion oncogene RBM15-MKL1.
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Date
2016-12-19
Authors
Ayllón, Verónica
Vogel-González, Marina
González-Pozas, Federico
Domingo-Reinés, Joan
Montes, Rosa
Morales-Cacho, Lucía
Ramos-Mejía, Verónica
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Abstract
Pediatric Acute Megakaryoblastic Leukemia not associated to Down Syndrome (non-DS AMKL) is a rare disease with a dismal prognosis. Around 15% of patients carry the chromosomal translocation t(1;22) that originates the fusion oncogene RBM15-MKL1, which is linked to an earlier disease onset (median of 6months of age) and arises in utero. Here we report the generation of two hPSC cell lines constitutively expressing the oncogene RBM15-MKL1, resulting in an increased expression of known RBM15-MKL1 gene targets. These cell lines represent new disease models of pediatric AMKL to study the impact of the RBM15-MKL1 oncogene on human embryonic hematopoietic development.
Description
MeSH Terms
Biomarkers
Cell Line
Child
Genetic Vectors
Humans
Leukemia, Megakaryoblastic, Acute
Models, Biological
Oncogene Proteins, Fusion
Pluripotent Stem Cells
Transcription Factors
Cell Line
Child
Genetic Vectors
Humans
Leukemia, Megakaryoblastic, Acute
Models, Biological
Oncogene Proteins, Fusion
Pluripotent Stem Cells
Transcription Factors