- Professor, Department of Medicine, Section of Hematology/Oncology
- Professor, UCCCC
- Professor, The Ben May Department for Cancer Research
- Professor, Committee on Cancer Biology
- Professor, Committee on Molecular Medicine/MPMM
- Professor, Committee on Molecular Metabolism and Nutrition
M.D., Yale University
The University of Chicago
900 East 57th Street
Chicago, Illinois 60637
Phone: (773) 834-2604
Webpage (Ben May)
Webpage (Medical Center)
Mammary Epithelial Cell Survival Signaling Pathways and the Role of Ubiquitin Modification in Regulating Kinase Activity
My laboratory studies molecular pathways in mammary epithelial cells that initiate inappropriate survival under conditions that would normally induce apoptosis, such as growth factor deprivation, chemotherapy and radiation. We have identified a novel survival pathway in these cells that is initiated through GR activation. Using large-scale gene array analysis, we have further identified several genes that are regulated by GR activation and are implicated in both novel and known survival signaling pathways. We are currently dissecting the individual contributions of the GR-regulated gene products to the survival phenotype. Understanding the mechanism of action of GR-mediated survival is proving to be a useful model for increasing both the understanding of gene regulation by the GR and the identification of novel survival pathways relevant to epithelial cells. These pathways are expected to identify novel targets for inhibitors that can interrupt the development of epithelial cell cancers (by blocking premalignant cell survival) and/or increase sensitivity to cytotoxic agents by increasing apoptosis.
Moran TJ, Gray S, Mikosz CA, Conzen SD. (2000). The glucocorticoid receptor mediates a survival signal in human mammary epithelial cells. Cancer Res. 60(4):867-72.
Conzen SD, Gottlob K, Kandel ES, Khanduri P, Wagner AJ, O'Leary M, Hay N. (2000). Induction of cell cycle progression and acceleration of apoptosis are two separable functions of c-Myc: transrepression correlates with acceleration of apoptosis. Mol Cell Biol. (16):6008-18.
Poelman SM, Adeyanju MO, Robertson MA, Recant WM, Karrison T, Fleming GF, Olopade OI, Conzen SD. (2000). Human breast cancer susceptibility to paclitaxel therapy is independent of Bcl-2 expression. Clin Cancer Res. (10):4043-8.
Mikosz CA, Brickley DR, Sharkey MS, Moran TW, Conzen SD. (2001). Glucocorticoid receptor-mediated protection from apoptosis is associated with induction of the serine/threonine survival kinase gene, sgk-1. J Biol Chem. 276(20):16649-54.
Brickley DR, Mikosz CA, Hagan CR, Conzen SD. (2002). Ubiquitin modification of serum and glucocorticoid-induced protein kinase-1 (SGK-1). J Biol Chem. [epub ahead of print]