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Chief, Surgical Services, VA Medical CenterProfessor of Surgery
- Gastrointestinal, Minimally-invasive and Bariatric Surgery
Primary Office: 1528 JCPIowa City, IA 52242
Primary Office Phone: 319-353-8297
MD, University of IowaBA, Loras College, Dubuque, IA
Residency, General Surgery, University of IowaFellowship, Digestive Disease, NIH Fellow, Mayo Clinic
Iowa Medical License (permanent), Iowa Board of MedicineBoard Certified, General Surgery, American Board of Surgery
Biosciences Graduate ProgramFree Radical and Radiation Biology Graduate ProgramInterdisciplinary Graduate Program in Translational BiomedicineMedical Scientist Training Program
Our research laboratory is focused on developing treatments for pancreatic cancer. Adenocarcinoma of the pancreas is the fourth leading cause of cancer death in the United States and is increasing in incidence. Our efforts are directed in two specific areas. 1. Dicumarol is a naturally occurring anticoagulant derived from coumarin, which is obtained from the sweet clover (Melilotus alba). Though such coumarin compounds as dicumarol have been utilized in cancer therapy, little is known about the mechanism of action of these drugs. Recent studies from our group have demonstrated that dicumarol induces cytotoxicty and oxidative stress in pancreatic cancer cells and this cytotoxicity appears to be more prominent in transformed vs. normal human fibroblasts. Mitochondria have been hypothesized to be the site of proxidant production during dicumarol treatment since dicumarol is thought to affect quinone-mediated electron transfer reactions leading to the production of superoxide (O2 .- ), and hydrogen peroxide (H2O2). Dicumarol-induced oxidative stress could represent a difference between tumor cell and normal cell mitochondrial metabolism amenable to manipulations designed to improve cancer therapy. To gain a mechanistic understanding of dicumarol-induced oxidative stress in pancreatic cancer cells, our laboratory investigates the hypothesis that mitochondrial production of reactive oxygen species (superoxide, hydrogen peroxide, and/or organic hydroperoxides) mediates the increased susceptibility of pancreatic cancer cells to dicumarol-induced metabolic oxidative stress, relative to normal human cells. 2. The objective of our second set of studies is to determine if antioxidant enzymes can be modulated for therapeutic purposes in pancreatic cancer. Signaling through the K-ras pathway in pancreatic cancer is related to treatment resistance. K-ras mutations have been identified in up to 95% of pancreatic cancers, implying their critical role in the molecular pathogenesis. Ras overexpression leads to increased plasma membrane-generated superoxide, which could be one mechanism regulating cell growth contributing to tumor progression. The objective of our studies is to determine if plasma membrane-generated superoxide can be modulated for therapeutic purposes in pancreatic cancer. Our central hypothesis is that scavenging of superoxide generated from the plasma membrane inhibits pancreatic cancer growth. Our hypothesis has been formulated on the basis of data demonstrating that scavenging of superoxide with the antioxidant enzymes extracellular superoxide dismutase (ECSOD) and copper/zinc superoxide dismutase (CuZnSOD), and small molecule superoxide scavengers have a strong tumor suppressive effect in pancreatic cancer. It is our expectation that the results will facilitate the discovery and development of targeted therapeutics against pancreatic cancer. Our laboratory is currently partially funded by grants from the National Institutes of Health.
Date Last Modified: 06/07/2014 -
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