CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemia

Author:

McNerney Megan E.12,Brown Christopher D.13,Wang Xiaoyue13,Bartom Elizabeth T.4,Karmakar Subhradip1,Bandlamudi Chaitanya15,Yu Shan15,Ko Jinkyung6,Sandall Barry P.6,Stricker Thomas7,Anastasi John2,Grossman Robert L.14,Cunningham John M.6,Le Beau Michelle M.18,White Kevin P.139

Affiliation:

1. Institute for Genomics and Systems Biology,

2. Department of Pathology,

3. Department of Human Genetics,

4. Center for Research Informatics,

5. Committee on Genetics, Genomics, and Systems Biology, and

6. Department of Pediatrics, Section of Hematology/Oncology and Stem Cell Transplantation, University of Chicago, Chicago, IL;

7. Department of Pathology, Microbiology, and Immunology, Vanderbilt University, Nashville, TN; and

8. Sections of Hematology/Oncology and

9. Genetic Medicine, University of Chicago, Chicago, IL

Abstract

Key PointsCUX1 is a transcription factor encoded on a region of chromosome 7 that is frequently deleted in high-risk acute myeloid leukemia. Haploinsufficiency of CUX1/cut promotes hematopoietic overgrowth in both Drosophila melanogaster and human xenograft mouse models in vivo.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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