Nondisjunction of chromosomes leading to hyperdiploid childhood B-cell precursor acute lymphoblastic leukemia is an early event during leukemogenesis

Author:

Panzer-Grümayer E. Renate1,Fasching Karin1,Panzer Simon1,Hettinger Klaudia1,Schmitt Klaus1,Stöckler-Ipsiroglu Sylvia1,Haas Oskar A.1

Affiliation:

1. From the Children's Cancer Research Institute; St Anna Kinderspital; Clinic for Blood Group Serology, University of Vienna; Landeskinderkrankenhaus Linz; and Austrian Newborn Screening Laboratory, Department of Pediatrics, University of Vienna; all of Austria.

Abstract

Abstract A hyperdiploid karyotype is found in 30% of B-cell precursor acute lymphoblastic leukemias in childhood. The time of nondisjunction of chromosomes leading to hyperdiploidy during leukemogenesis is unknown. We used the 3 clonotypic immunoglobulin heavy chain (IgH) gene rearrangements as molecular markers for each of the 3 chromosomes 14 in a case with hyperdiploid acute lymphoblastic leukemia to define the order of events—namely, somatic recombination and nondisjunction of chromosomes—during leukemia development. A partial sequence homology of the incomplete DJH rearrangement with 1 of the 2 nonfunctional VDJH rearrangements suggests that the doubling of chromosomes had occurred after this DJHrearrangement and thus during early B-cell differentiation. The occurrence of the nondisjunction of chromosomes as well as ongoing rearrangement processes in utero were confirmed by the presence of all 3 IgH rearrangements in neonatal blood spots, providing the first evidence that hyperdiploidy formation is an early event in leukemogenesis in these leukemias.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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