The Hippo signaling pathway is a developmentally conserved pathway involved in organ size control, cellular proliferation and differentiation. Multiple lines of evidence suggest that deregulation of Hippo signaling plays a role in pancreatic cancer, include frequent overexpression of hYAP, the nuclear effector of mammalian Hippo signaling, in pancreatic cancer tissues and cell lines, and less commonly, somatic mutations of hFAT1 and hFAT4, human orthologs of a Drosophila cadherin gene involved in Hippo repression and growth suppression. Ectopic hYAP expression in non-tumorigenic human pancreatic epithelial cells transforms these cells, while knockdown of endogenous hYAP by RNA interference in pancreatic cancer lines inhibits in vivo growth in athymic mice. The transcriptional targets of hYAP in human cells include genes associated with invasion, metastases, and tumor angiogenesis, as well as a limited cache of cancer-associated microRNAs (miRNAs). This proposal will provide functional annotation vis-a-vis the Hippo pathway in pancreatic cancer initiation and maintenance, using a variety of preclinical models. Specifically, in Aim 1, a role for Hippo pathway in pancreatic progenitor cell expansion will be studied using transgenic zebrafish with ectopic hYAP expression in the exocrine pancreas. The zebrafish studies will also elucidate whether common oncogenic and represser mutations found in human pancreatic cancer demonstrate genetic cooperation with hYAP in inducing pancreatic neoplasia.
In Aim 2, modulation of Hippo signaling will be studied in mammalian systems. Specifically, Yap will be conditionally ablated in a compound transgenic mouse model of pancreatic neoplasia and the effects on natural history of the disease and immunophenotype of resulting pancreatic lesions studied. Further, a panel of isogenic human pancreatic cancer lines will be generated by engineering missense mutations of hFAT1 and hFAT4 at their endogenous loci, in order to study the biochemical mechanisms associating the membrane bound FAT protocadherins to intracellular events in the Hippo pathway. Lastly, in Aim 3, hYAP-regulated miRNAs will be analyzed for their ability to recapitulate or rescue the phenotype of aberrant Hippo signaling in pancreatic cancer.

Public Health Relevance

Pancreatic cancer is a lethal disease and the understanding of altered signaling pathways will provide avenues for therapy and early diagnosis. We will study the role of Hippo signaling, which has been implicated throughout evolution in growth and size control, with regards to its role in pancreatic cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA134292-05
Application #
8464661
Study Section
Special Emphasis Panel (ZCA1-GRB-S)
Project Start
2013-04-01
Project End
2014-03-31
Budget Start
2013-04-01
Budget End
2014-03-31
Support Year
5
Fiscal Year
2013
Total Cost
$334,090
Indirect Cost
$129,508
Name
Johns Hopkins University
Department
Type
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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