Awardee OrganizationPENNSYLVANIA STATE UNIV HERSHEY MED CTR
Description
Abstract Text
Pancreatic cancer is a devastating disease that occurs in nearly
30,000 Americans annually and is the fifth leading cause of cancer-related
deaths in the United States. From the time of diagnosis the median survival for
patients with pancreatic cancer is approximately 3 to 6 months. The reasons for
this aggressive behavior include the inability to detect patients with this
malignancy at early stages, resistance to standard chemotherapy, and a poor
understanding of the mechanisms involved in growth regulation of pancreatic
cancer. Peptides of the CCK-gastrin family have been shown to stimulate growth
of pancreatic cancer through selective CCK-like receptors and blockade of this
receptor with antagonists results in growth indeed be unique. Unlike many other
cultured cells, pancreatic cancer cells thrive readily in growth media deprived
of serum since they produce gastrin, which in turn regulates growth of this
cancer in a tonic and autocrine fashion. Based upon her preliminary findings,
she puts forth the hypothesis that the growth of human pancreatic cancer is
mediated through a unique CCK-like receptor, dependent upon gastrin and/or CCK,
and that deprivation of these peptides will inhibit growth of this malignancy.
In order to test this hypothesis it is proposed to 1) determine the biological
form of gastrin and /or CCK involved in pancreatic cancer growth by performing
growth studies, Reverse-phase HPLC, and radioimmunoassay, 2) characterize the
differences between peptides and receptor expression of human pancreas cancer
tissues and normal pancreas tissues, 3) study the functional significance of
CCK/gastrin gene expression by stable transfections of these peptides into
pancreatic cancer cells, 4) characterize the molecular properties of the
receptor by cloning and sequencing the receptor, and 5) examine the functional
significance of the unique CCK-like receptor by examining it's over and under
expression in stable transfected cell lines. These studies are part of the
team's long-term goal to understand the mechanisms involved in the biology of
human pancreatic cancer, and contribute to the treatment and early detection of
this malignancy.
No Sub Projects information available for 5R01CA085713-04
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5R01CA085713-04
Patents
No Patents information available for 5R01CA085713-04
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 5R01CA085713-04
Clinical Studies
No Clinical Studies information available for 5R01CA085713-04
News and More
Related News Releases
No news release information available for 5R01CA085713-04
History
No Historical information available for 5R01CA085713-04
Similar Projects
No Similar Projects information available for 5R01CA085713-04