Human acute stem cell leukemia with multilineage differentiation potential via cascade activation of growth factor receptors

Author:

Testa Ugo1,Torelli Giovanni F.1,Riccioni Roberta1,Muta Andrea Onetti1,Militi Stefania1,Annino Luciana1,Mariani Gualtiero1,Guarini Anna1,Chiaretti Sabina1,Ritz Jerome1,Mandelli Franco1,Peschle Cesare1,Foa Robin1

Affiliation:

1. From the Department of Hematology-Oncology, Istituto Superiore di Sanità, Rome, Italy; the Department of Cellular Biotechnologies and Hematology and the Department of Experimental Medicine and Pathology, University of Rome La Sapienza, Italy; the Department of Adult Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA; and the Kimmel Cancer Institute, Thomas Jefferson University, Philadelphia, PA.

Abstract

The morphologic, immunophenotypic, genotypic, genomic, and functional features of an undifferentiated acute leukemia with stem cell features are reported. At light and electron microscopy, the leukemic population was represented by primitive progenitor cells with no evidence of differentiation. The blasts were CD34+, AC133+, CD71−, HLA-DR−, CD38−/dim+, CD90+, CD117dim+, flt3+; did not express B, T, or myeloid-associated antigens; and showed a germline configuration of the immunoglobulin and T-cell receptor. Genomic profiling documented the expression of early stem cell and myeloid-associated genes. Receptors for early-acting hemopoietic growth factors (HGFs) were detected, while receptors for unilineage HGF were not expressed. Incubation with the flt3 or Kit ligand induced the expression of unilineage HGF receptors, allowing these cells to respond to their respective ligands. Growth without differentiation was sustained only in the presence of early-acting HGF, namely flt3 ligand, while early and unilineage HGF gave rise to all types of hemopoietic colonies.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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