Steve Kridel Lab

 

Education:

B.S. California State University, Los Angeles, 1992 
Ph.D. University of California, Irvine, 1997
Postdoctoral training, The Burnham Institute, La Jolla, CA, 1997-2002

Research Interests:

Fatty acid synthase
The primary research focus of the Kridel laboratory is to understand the role of fatty acid synthesis in tumors. Specifically, we are interested in how fatty acid synthase (FAS), the enzyme that catalyzes the terminal steps of fatty acid synthesis, contributes to tumor progression and the anti-tumor mechanisms of FAS inhibitors, especially in prostate cancer. FAS is expressed at high levels in tumors and expression levels correlate with disease progression and recurrence. The enzyme is unique in that it encodes seven functional domains that work in concert to generate fatty acid. We were the first to identify Orlistat as an inhibitor of the thioesterase domain of FAS. Inhibition of FAS induces cell death in a range of tumor cell lines and inhibits the growth of prostate tumor xenografts in mice. Our recent work has focused on understanding the mechanism of action of orlistat and other FAS inhibitors. Work by our group has demonstrated that FAS is required for proper function of the endoplasmic reticulum (ER) in tumor cells and that FAS inhibitors induce ER stress in tumor cells. Current studies are aimed at understanding how the ER stress response may regulate the cell death response when FAS is inhibited. We believe these data provide a teleological link between FAS expression and tumors. In addition, we are also interested in understanding the role of acetyl-CoA carboxylase (ACC) in cancer. ACC catalyzes the rate limiting step in fatty acid biosynthesis. We have made the novel observation that ACC is required for the formation of podosomes and we are interested in understanding the mechanism for this.

Structural Biology

We are also interested in understanding how Orlistat inhibits FAS and using such information to possibly develop new and more effective FAS inhibitors. In collaboration with the Lowther laboratory in the Department of Biochemistry, we have solved the structure of the thioesterase domain of FAS bound by orlistat. This crystal structure represents the first structure of any domain of human FAS bound to a ligand. The resulting data not only provides a blueprint for the development of novel inhibitors, they may also provide a primer to understand how the thioesterase domain recognizes and cleaves growing fatty acyl chains from the FAS polypeptide. Orlistat may acts as a substrate mimetic of palmitoyl-CoA or –ACP and may occupy the same cavity as the natural substrate. In addition, we have an ongoing drug-discovery project aimed at identifying and optimizing novel FAS inhibitors for therapeutic development.

NAD Biosynthesis and Prostate Cancer

There is growing evidence to suggest that NAD is important in cancer. There are multiple mechanisms by which cell obtain or synthesize NAD and multiple pathways that utilize NAD, either as a cofactor or as a substrate. We are interested in understanding the role of NAD in prostate cancer cells and defining the mechanisms by which prostate cancer cells obtain NAD. Specifically we are interested in how Nampt regulates tumor cell survival and metabolism. In addition, we are interested in determining an “NAD fingerprint” in tumor cells through metabolic, lipidomic and genomic profiles.

Recent Publications

Kridel, S.J., Axelrod, F., Rozenkrantz, N., and Smith, J.W. Orlistat is a Novel Inhibitor of Fatty Acid Synthase with Antitumor Activity. (2004) Cancer Research, 64(6):2070-5.
Weiling Zhao, Steven Kridel, Andrew Thorburn, Joy Little, Sachidanaa Hebbar and Mike E. Robbins, Fatty acid synthase: a novel target for anti-glioma therapy (2006)British Journal of Cancer, 95(7):869-78.
Little, J.L., Wheeler, F.B., Fels, D., Koumenis, C., and Kridel, S.J. Fatty Acid Synthase Inhibitors Induce Endoplasmic Reticulum Stress Tumor Cells (2007) Cancer Research, 67(3):1-8.
Pemble, C.W., Johnson, L.C., Kridel, S.J., and Lowther W.T., Crystal structure of the thioesterase domain of human fatty acid synthase inhibited by Orlistat. (2007) Nature Structural and Molecular Biology 14(8): 704-709.
Lally, B.E., Geiger, G.A., Kridel, S.J., Arcury-Quandt, A. E., Robbins, M.E., Kock, N.D., Wheeler, K., Prakash, P., Georkakilas, A., Kao, G.D., and Koumenis C. Identification and preclinical characterization of a novel and potent small molecule radiation sensitizer via an unbiased screen of a chemical library (2007) Cancer Research 67(18): 8791-9.
Chen Y.Q., Edwards, I.J., Kridel, S.J., Thornburg, T., and Berquin, I.M. Dietary fat-gene interactions in cancer. (2007) Cancer and Metastasis Reviews 26(3-4):535-551.
Kridel, S.J., Lowther, W.T., and Pemble, C.W. Fatty acid synthase inhibitors: new directions for oncology. Expert Opinion on Investigational Drugs (2007) 16(11): 1817-29.
Vāvere AL, Kridel SJ, Wheeler FB, Lewis JS. 1-11C-Acetate as a PET Radiopharmaceutical for Imaging Fatty Acid Synthase Expression in Prostate Cancer. Journal of Nuclear Medicine, 49:327-334, 2008.
Little J.L. and Kridel, S.J. Fatty Acid Synthase Activity in Tumor Cells. (2008) In Subcellular Biochemistry: Lipids in Health and Disease, (PJ Quinn, X Wang, eds.), Springer, 49:169-194.
Fels, D.R., Ye, J. Segan, A.T., Kridel, S.J., Spiotto, M., Olson, M., Koong, A.C., and Koumenis, C. Preferential cytotoxicity of bortezomib towards hypoxic cells via over activation of ER stress pathways (2008) Cancer Research, 68(22):9323-30.
Little, J.L., Wheeler, F.B., Koumenis, C.,and Kridel. S.J. Disruption of crosstalk between the fatty acid synthesis and proteasome pathways enhances unfolded protein response signaling and cell death. (2008) Molecular Cancer Therapeutics,7:3816-3824

 

Quick Reference

Cancer Biology

Telephone 336-716-9132

Fax 336-716-0255

E-mail
bbottoms@wakehealth.edu
Graduate Program E-mail
skridel@wakehealth.edu

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