Therapy-related leukemias following treatment with drugs that target DNA toposiomerase II frequently involve translocations of the MLL gene on chromosome band 11q23. This research project will focus on functional analysis of MLL translocations, with a major focus on the MLL-CBP translocation. MLL-CBP was cloned as the MLL fusion present in patients with a t(11;16) (q23;p13). With one exception, these patients had therapy-related leukemia, and a substantial proportion presented with t-MDS. We recently developed murine model systems for the in vitro and in vivo analysis of the MLL-CBP fusion. This project involves studies to further delineate critical functions contributed by CBP to the fusion protein, to determine the functional effects of domain swapping on leukemia and pre-leukemia phenotype, and to determine the effects of the MLL-CBP fusion on hematopoietic cell lineage commitment and survival.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA095040-02
Application #
6622984
Study Section
Special Emphasis Panel (ZRG1-PTHC (01))
Program Officer
Mufson, R Allan
Project Start
2002-04-20
Project End
2003-04-30
Budget Start
2003-04-11
Budget End
2003-04-30
Support Year
2
Fiscal Year
2003
Total Cost
$21,953
Indirect Cost
Name
Loyola University Chicago
Department
Obstetrics & Gynecology
Type
Schools of Medicine
DUNS #
791277940
City
Maywood
State
IL
Country
United States
Zip Code
60153
Santillan, Donna A; Theisler, Catherine M; Ryan, Amanda S et al. (2006) Bromodomain and histone acetyltransferase domain specificities control mixed lineage leukemia phenotype. Cancer Res 66:10032-9