Certain phorbol esters, polar solvents and cytokines have been identified as in vitro inducers of human myeloid leukemic cell differentiation. However, the mechanisms by which these diverse groups of agents induce terminal maturation remain unclear. Furthermore, it is not clear whether agents that induce differentiation in vitro exert similar effects in vivo. The proposed studies will address these two related issues. Few insights are presently available regarding the intracellular signaling events activated by inducers of leukemic cell differentiation. However, recent studies suggest that the diverse classes of inducers similarly stimulate arachidonic acid metabolism during the induction of monocytic differentiation. The proposed studies will focus on the intracellular signaling events associated with phospholipid hydrolysis, appearance of the monocytic phenotype and changes in specific gene expression. The proposed studies will also continue to examine the therapeutic effects of differentiating agents in the treatment of myelodysplastic syndromes and acute myeloid leukemia. The induction of differentiation in vivo will be assessed by monitoring clonality of leukemic blasts and peripheral blood cells.
The specific aims are: 1) to determine intracellular signaling mechanisms associated with induction of monocytic differentiation by agents that activate protein kinase C: 2) to study signal transduction pathways induced by polar solvent during myeloid differentiation; 3) to examine the effects of specific cytokines on induction of both intracellular signaling mechanisms and monocytic differentiation; and 4) to further study the effects of differentiating agents in the therapy of acute myeloid leukemia. These studies should provide fundamental insights regarding the intracellular signaling events induced by agents which overcome the block in leukemic cell differentiation. This work should also contribute to our understanding of the in vivo therapeutic effects of agents that induce differentiation in vitro.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA042802-04
Application #
3184354
Study Section
Experimental Therapeutics Subcommittee 1 (ET)
Project Start
1986-08-01
Project End
1993-01-31
Budget Start
1990-02-01
Budget End
1991-01-31
Support Year
4
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Dana-Farber Cancer Institute
Department
Type
DUNS #
149617367
City
Boston
State
MA
Country
United States
Zip Code
02215
Jain, Salvia; Stroopinsky, Dina; Yin, Li et al. (2015) Mucin 1 is a potential therapeutic target in cutaneous T-cell lymphoma. Blood 126:354-62
Raina, Deepak; Agarwal, Praveen; Lee, James et al. (2015) Characterization of the MUC1-C Cytoplasmic Domain as a Cancer Target. PLoS One 10:e0135156
Yin, Li; Kufe, Turner; Avigan, David et al. (2014) Targeting MUC1-C is synergistic with bortezomib in downregulating TIGAR and inducing ROS-mediated myeloma cell death. Blood 123:2997-3006
Liu, Suiyang; Yin, Li; Stroopinsky, Dina et al. (2014) MUC1-C oncoprotein promotes FLT3 receptor activation in acute myeloid leukemia cells. Blood 123:734-42
Liu, Yan; Marks, Kevin; Cowley, Glenn S et al. (2013) Metabolic and functional genomic studies identify deoxythymidylate kinase as a target in LKB1-mutant lung cancer. Cancer Discov 3:870-9
Stroopinsky, Dina; Rosenblatt, Jacalyn; Ito, Keisuke et al. (2013) MUC1 is a potential target for the treatment of acute myeloid leukemia stem cells. Cancer Res 73:5569-79
Jin, C; Rajabi, H; Rodrigo, C M et al. (2013) Targeting the eIF4A RNA helicase blocks translation of the MUC1-C oncoprotein. Oncogene 32:2179-88
Jin, Caining; Rajabi, Hasan; Pitroda, Sean et al. (2012) Cooperative interaction between the MUC1-C oncoprotein and the Rab31 GTPase in estrogen receptor-positive breast cancer cells. PLoS One 7:e39432
Ahmad, Rehan; Alam, Maroof; Rajabi, Hasan et al. (2012) The MUC1-C oncoprotein binds to the BH3 domain of the pro-apoptotic BAX protein and blocks BAX function. J Biol Chem 287:20866-75
Raina, Deepak; Ahmad, Rehan; Rajabi, Hasan et al. (2012) Targeting cysteine-mediated dimerization of the MUC1-C oncoprotein in human cancer cells. Int J Oncol 40:1643-9

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