Keywords:
Acute lymphoblastic leukemia; B-ALL; ELOVL1; infant leukemia; MLL-AF4; onco-fetal signature; PLK1
Abstract:
Infant MLL-AF4-driven acute lymphoblastic leukemia (ALL) is a devastating disease with dismal prognosis. A lack of understanding of the unique biology of this disease, particularly its prenatal origin, has hindered improvement of survival. We perform multiple RNA sequencing experiments on fetal, neonatal, and adult hematopoietic stem and progenitor cells from human and mouse.