Phytochemicals and Metabolism in Pancreatic Diseases

Principle Investigator: Stephen J. Pandol, MD
Co-Principle Investigator: Anna S. Gukovskaya, PhD
Co-Investigator: Ilya Gukovsky, PhD
Co-Investigator: Aurelia Lugea, PhD
Co-Investigator: HongXiang Hui, MD PhD
Postdoctoral Fellow: Mouad Edderkaoui, PhD

Hypothesis: We propose that certain phytochemical decrease proliferation of stellate cells and cancer cells at least in part by inhibiting ROS-regulated pentose cycle pathways, resulting in decreased nucleic acid synthesis, decreased proliferation and increased apoptosis.

The Exocrine Pancreas and the Stellate Cell

The Exocrine Pancreas and the Stellate Cell

Stellate Cells Mediate Ethanol-Induced Pancreatic and Liver Disease

Stellate Cells Mediate Ethanol-Induced Pancreatic and Liver Disease

Roles of Pancreatic Stellate Cells in Carcinogenesis

Roles of Pancreatic Stellate Cells in Carcinogenesis

Specific Aims for Stellate and Cancer Cells in Vitro

  1. Determine the effects of selected phytochemicals on ROS production, glucose metabolism, DNA synthesis, proliferation and apoptosis.
  2. Determine the effects of pharmacologic and genetic inhibition of ROS production on glucose metabolism, DNA synthesis, proliferation and apoptosis.


Specific Aims for Experimental Animal Models

  1. Determine the effects of selected phytochemicals on progression of the pathologic processes in chronic pancreatitis.
  2. Determine the ability of selected phytochemicals to prevent the initiation and/or progression of pancreatic cancer.

Specific Aims for Experimental Animal Models

Several Cell Proteins Regulate Apoptosis