IKZF1 Alterations and Therapeutic Targeting in B-Cell Acute Lymphoblastic Leukemia

Author:

Paolino Jonathan12ORCID,Tsai Harrison K.3,Harris Marian H.3,Pikman Yana12ORCID

Affiliation:

1. Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA

2. Division of Hematology/Oncology, Boston Children’s Hospital, Boston, MA 02115, USA

3. Department of Pathology, Boston Children’s Hospital, Boston, MA 02115, USA

Abstract

IKZF1 encodes the transcription factor IKAROS, a zinc finger DNA-binding protein with a key role in lymphoid lineage development. IKAROS plays a critical role in the development of lineage-restricted mature lymphocytes. Deletions within IKZF1 in B-cell acute lymphoblastic leukemia (B-ALL) lead to a loss of normal IKAROS function, conferring leukemic stem cell properties, including self-renewal and subsequent uncontrolled growth. IKZF1 deletions are associated with treatment resistance and inferior outcomes. Early identification of IKZF1 deletions in B-ALL may inform the intensification of therapy and other potential treatment strategies to improve outcomes in this high-risk leukemia.

Funder

Boston Children’s Hospital Translational Research Program

Wong Family Award in Translational Oncology

Alex’s Lemonade Stand Foundation

Hyundai Hope on Wheels Scholar

Julia’s Legacy of Hope St. Baldrick’s Foundation Consortium Research

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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