The long term objective of the project is to further the current understanding and development of novel cancer chemopreventive agents. The goal of this proposal is to determine the molecular mechanism of a promising class of cancer chemopreventives.
Our first aim i s to determine the binding mode of CDDO, a small molecule which pharmacologically inhibits the expression of iNOS and COX-2. We will generate antibodies against a CDDO-hapten, evaluate their specificity using western blot techniques, and use these antibodies to identify if CDDO forms covalent protein adducts. If CDDO adducts are identified, we will attempt to identify cognate binding proteins using traditional biochemical fractionation guided by western blot analysis and protein identification using mass spectrometry techniques. If covalent interaction is not observed, the anti-CDDO antibodies will be used in conjunction with a photoaffinity labeling technique to identify relevant interactions.
The second aim i s to study the structural requirements for CDDO activity by expanding the collection of CDDO-like chemopreventives using a unique approach of diversity oriented synthesis (DOS). We would like to expand the repertoire of molecules which pharmacologically knock down expression of key inflammatory enzymes iNOS and COX-2. Structural homologs of CDDO will be used as a platform for DOS. Structure activity relationships will be conducted by monitoring changes in expression of iNOS and COX-2 using Griess assay and western blot techniques. Evaluation of the activity of these structural homologs will aid in the determination of mechanisms mediating the activity of CDDO and the molecular basis of the therapeutic properties of this molecule. Successful completion of these studies will advance the development of novel chemopreventive agents that could potentially be introduced into clinical trials.
We hope to move the field of cancer chemoprevention forward by providing new information on the biology and chemistry of one of the most promising class of chemopreventive agents. Our study will help facilitate more members of this family entering the clinic to help improve patient outcome through early intervention and also reduce the risk of second malignancies for cancer survivors.
| Gatbonton-Schwager, Tonibelle N; Sadhukhan, Sushabhan; Zhang, Guo-Fang et al. (2014) Identification of a negative feedback loop in biological oxidant formation fegulated by 4-hydroxy-2-(E)-nonenal. Redox Biol 2:755-63 |
| Gatbonton-Schwager, Tonibelle N; Letterio, John J; Tochtrop, Gregory P (2012) Bryonolic acid transcriptional control of anti-inflammatory and antioxidant genes in macrophages in vitro and in vivo. J Nat Prod 75:591-8 |
| Barker, Emily C; Gatbonton-Schwager, Tonibelle N; Han, Yong et al. (2010) Bryonolic acid: a large-scale isolation and evaluation of heme oxygenase 1 expression in activated macrophages. J Nat Prod 73:1064-8 |
