Karen Coschigano, PhD
Associate Professor, Molecular/Cellular Biology
Academic Research Center 302D
Member Type: Investigator
The main research focus of my laboratory is the identification of genes, proteins and regulatory pathways involved in the development of diabetic nephropathy, with an emphasis on the roles of growth hormone, signal transducer and activator of transcription 5 (STAT5), and inflammation. My group uses mouse models, cell culture and molecular techniques, including microarray analyses and real-time RT/PCR. We correlate changes in gene expression with changes in kidney function and histomorphometric parameters (the latter performed in collaboration with Dr. Ramiro Malgor, a colleague in my department). We expect this knowledge to aid in the design of more specific, targeted markers and therapeutic approaches for the diagnosis, treatment or prevention of human diabetic kidney disease.
Coschigano, K. T., Wetzel, A. N., Obichere, N., Sharma, A., Lee, S., Rasch, R., … Kopchick, J. J. (2010). Identification of differentially expressed genes in the kidneys of growth hormone transgenic mice. Growth Hormone & IGF Research: Official Journal of the Growth Hormone Research Society and the International IGF Research Society, 20(5), 345–355.
Coschigano, K. T. (2006). Aging-related characteristics of growth hormone receptor/binding protein gene-disrupted mice. Age (Dordrecht, Netherlands), 28(2), 191–200.
Coschigano, K. T., Holland, A. N., Riders, M. E., List, E. O., Flyvbjerg, A., & Kopchick, J. J. (2003). Deletion, but not antagonism, of the mouse growth hormone receptor results in severely decreased body weights, insulin, and insulin-like growth factor I levels and increased life span. Endocrinology, 144(9), 3799–3810.