Pancreatic ductal adenocarcinoma (PDAC), which accounts for 85% of pancreatic cancer, is one of the most lethal cancers with limited therapeutic options. Epigenetic therapy holds tremendous promise in cancer therapeutics. It depends on small molecules that can modulate chromatin status thereby altering disease phenotypes. Developing novel epigenetic therapy tailored for PDAC treatment will open up unprecedented possibility for improving patient survival and life quality. However, so far, the potential of epigenetic drugs for treating PDAC remains to be fully explored. Through screening of a panel of epigenetic drugs, histone deacetylase (HDAC) inhibitor MS275 (MS, also called entinostat) has been shown to have potent anti-PDAC effects. MS not only suppresses tumor cell proliferation but also inhibits the activation of stromal pancreatic stellate cells (PSCs) in vitro and in vivo. This project aims to investigate how MS regulates the tumor cell and stromal compartments in PDAC, and to comprehensively assess the therapeutic potential of MS with animal models. To achieve these aims, an experimental platform based on orthotopic transplantation and fluorescence-activated cell sorting (FACS) is established for isolating cells of individual PDAC compartments from in vivo developed tumors.
Aim 1 of the proposal will define the molecular mechanism underlying the anti- proliferative effect of MS on tumor cells, focusing on its role in regulating gene expression and the epigenomes.
Aim 2 will investigate how MS inhibits PSC activation and how it affects immune cell infiltration in the tumor microenvironment.
Aim 3 will assess the therapeutic potential of MS as a single agent or in combination with chemotherapy and/or immune check point therapy, using orthotopic transplantation and genetically engineered mouse model (GEMM) of PDAC. It will also evaluate the potential of MS for treating or preventing chronic pancreatitis, a disease condition involving PSC activation and predisposing to PDAC. Completion of the proposed studies will not only establish novel epigenetic therapy for pancreatic cancer, but also reveal the mechanisms contributing to its therapeutic benefit.

Public Health Relevance

Pancreatic cancer is one of the most fatal cancers that have almost no effective therapy. One potential approach to combat this deadly disease involves a class of chemicals called ?epigenetic drugs?, which have the capacity to change cellular states. This project aims to evaluate the therapeutic potential of epigenetic drugs and understand the mechanism underlying the potential.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32CA217033-01
Application #
9329169
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Jakowlew, Sonia B
Project Start
2017-04-01
Project End
2020-03-31
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Salk Institute for Biological Studies
Department
Type
DUNS #
078731668
City
La Jolla
State
CA
Country
United States
Zip Code
92037