RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM)

• Autores: Schlegelberger, Brigitte; Heller, Paula Graciela
• Año de publicación: 2017
• Idioma: inglés
• Tipo de recurso: artículo
• Materia: RUNX1; FAMILIAL PLATELET DISORDER; HEREDITARY MYELOID MALIGNANCIES; PREDISPOSITION TO LEUKEMIA
• Institución: Consejo Nacional de Investigaciones Científicas y Técnicas

In this review, we discuss disease-causing alterations of RUNT-related transcription factor 1 (RUNX1), a master regulator of hematopoietic differentiation. Familial platelet disorder with predisposition to myeloid leukemia (FPDMM) typically presents with (1) mild to moderate thrombocytopenia with normal-sized platelets; (2) functional platelets defects leading to prolonged bleeding; and (3) an increased risk to develop myelodysplastic syndromes (MDS), acute myeloid leukemia (AML), or T-cell acute lymphoblastic leukemia (T-ALL). Hematological neoplasms in carriers of a germline RUNX1 mutation need additional secondary mutations or chromosome aberrations to develop. If a disease-causing mutation is known in the family, it is important to prevent hematopoietic stem cell transplantation from a sibling or other relative carrying the familial mutation. First experiments introducing a wild-type copy of RUNX1 into induce pluripotent stem cells (iPSC) lines from patients with FPDMM appear to demonstrate that by gene correction reversal of the phenotype may be possible.
Fil: Schlegelberger, Brigitte. Hannover Medical School. Department of Human Genetics; Alemania
Fil: Heller, Paula Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina