description). This application proposes to investigate analogs of vitamin D3, (1,25D3) in combinations with antileukemia agents such as arabinocytosine or etoposide and related compounds. The cellular responses to D3 analogs and drug combinations will be monitored for changes in the cell cycle traverse and the expression of genes which control this traverse by transduction of signals for growth, differentiation, and programmed cell death. The genes studied will include those encoding the regulatory subunits of cell cycle dependent protein kinase complexes, i.e., cyclins D, E, A, and B, and inhibitors of this activity, proteins p16 and p21. Transduction of signals initiated by these analogs will also be assessed by determinations of intracellular calcium, by changes in the expression and activity of calcium, phospholipid-activated protein kinase C, and by evaluation of the ability of PKC to increase the activity and upregulated the expression of the plasma membrane calcium pump. These approaches are intended to increase the understanding of the cellular actions of VD3 analogs, and to provide a basis for better design of clinical trails now being initiated.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA044722-10A1
Application #
2731832
Study Section
Experimental Therapeutics Subcommittee 1 (ET)
Program Officer
Forry, Suzanne L
Project Start
1987-06-01
Project End
2002-12-31
Budget Start
1999-02-10
Budget End
1999-12-31
Support Year
10
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Pathology
Type
Schools of Medicine
DUNS #
605799469
City
Newark
State
NJ
Country
United States
Zip Code
07107
Wang, Xuening; Beute, William K; Harrison, Jonathan S et al. (2018) JNK1 as a signaling node in VDR-BRAF induction of cell death in AML. J Steroid Biochem Mol Biol 177:149-154
Zheng, Ruifang; Studzinski, George P (2017) Nuclear ERK5 inhibits progression of leukemic monocytes to macrophages by regulating the transcription factor PU.1 and heat shock protein HSP70. Leuk Lymphoma 58:1468-1480
Zheng, Ruifang; Studzinski, George P (2017) Optimal AraC-Cytotoxicity to AML Cells Requires ERK5 Activity. J Cell Biochem 118:1583-1589
Wang, Xuening; Harrison, Jonathan S; Studzinski, George P (2017) BRAF signals to pro-apoptotic BIM to enhance AraC cytotoxicity induced in AML cells by Vitamin D-based differentiation agents. J Steroid Biochem Mol Biol 173:139-147
Harrison, Jonathan S; Wang, Xuening; Studzinski, George P (2016) The role of VDR and BIM in potentiation of cytarabine-induced cell death in human AML blasts. Oncotarget 7:36447-36460
Wang, Xuening; Harrison, Jonathan S; Studzinski, George P (2016) Enhancement of arabinocytosine (AraC) toxicity to AML cells by a differentiation agent combination. J Steroid Biochem Mol Biol 164:72-78
Gocek, El?bieta; Studzinski, George P (2016) DNA Repair in Despair-Vitamin D Is Not Fair. J Cell Biochem 117:1733-44
Pesakhov, Stella; Nachliely, Matan; Barvish, Zeev et al. (2016) Cancer-selective cytotoxic Ca2+ overload in acute myeloid leukemia cells and attenuation of disease progression in mice by synergistically acting polyphenols curcumin and carnosic acid. Oncotarget 7:31847-61
Studzinski, George P; Harrison, Jonathan S; Wang, Xuening et al. (2015) Vitamin D Control of Hematopoietic Cell Differentiation and Leukemia. J Cell Biochem 116:1500-12
Wang, Xuening; Pesakhov, Stella; Harrison, Jonathan S et al. (2015) The MAPK ERK5, but not ERK1/2, inhibits the progression of monocytic phenotype to the functioning macrophage. Exp Cell Res 330:199-211

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