There are two parallel overall objectives of this proposal. One is to further delineate the molecular mechanisms that give rise to the antitumor efficacy of three groups of agents, of which two are in phase II clinical trials and the third shows promising in vivo activity. The second is to validate and then use differential gene expression technology to guide the course of research that will pinpoint the molecular mechanisms for the antitumor activity of the same three groups of compounds. The specific objectives of the proposed research are to: 1. design and synthesize a series of fluoroquinolones with a dual mechanism of action so that different members of the series are optimized for one or the other of the activities and others have both activities. 2. determine the structural and biochemical effects of Et 743, a DNA-reactive drug with phase II clinical activity. 3. determine the mechanism of action of HMAF, a phase II clinical trial candidate with an unknown mechanism of action. 4. design experiments to interpret patterns of differential gene expression from the agents in specific aim 1 and use this information to guide the course of experiments in Specific Aims 2 and 3. In order to achieve these objectives, a variety of techniques, including design and synthesis of small molecular weight molecules, high-field NMR and molecular modeling, gel electrophoresis, and DNA microchip array analysis, will be used.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
3R01CA088310-02S1
Application #
6493126
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Program Officer
Rosenfeld, Bobby
Project Start
2000-05-01
Project End
2005-04-30
Budget Start
2001-05-01
Budget End
2002-04-30
Support Year
2
Fiscal Year
2001
Total Cost
$52,504
Indirect Cost
Name
University of Arizona
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
City
Tucson
State
AZ
Country
United States
Zip Code
85721
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