HPK1, also named MAP4K1, is a mammalian Ste20-related serine/threonine kinase and has been shown to inhibit Erk and activate NF?B and JNK pathways (1). While a number of studies have identified the role of HPK1 in proliferation, differentiation and apoptosis in hematopoietic cells, the role of HPK1 in malignant transformation, proliferation, and invasion in malignancies has not been examined. Recently, we demonstrated that HPK1 protein is expressed in normal pancreatic ducts, but is lost in >95% of pancreatic ductal carcinoma (PDC) samples. The loss of HPK1 protein is strongly associated with the progression from low-grade pancreatic intraepithelial neoplasia (PanIN) to invasive PDC. More importantly, restoring wild type HPK1 protein expression in PDC cells resulted in cell cycle arrest and growth inhibition, which is due in part to up- regulation of p21 and p27 (2). Thus, our data showed, for the first time, that HPK1 may function as a novel tumor suppressor and its loss plays a critical role in the development of PDC. In addition, we have also demonstrated that loss of HPK1 in PDC is due to proteasome-mediated protein degradation, but not at the mRNA levels and that HPK1 kinase activity is required for the loss of HPK1 protein in PDC (2). Little is known about the regulation of HPK1 in vivo. Recently, we have identified Fbw8 as the E3 ligase that is responsible for proteasome-mediated degradation of HPK1 protein in PDC. In this proposal, we will examine the novel molecular mechanisms by which Fbw8 targets HPK1 protein for degradation and the oncogenic functions of Fbw8 in pancreatic cancer. Accomplishment of the proposed studies will not only reveal the novel molecular pathways of HPK1 regulation in pancreatic cancer, but also identify new targets for pancreatic cancer treatment. We have the following two Specific Aims:
Specific Aim 1 : To examine the mechanism of ubiquitin E3 ligase, Fbw8, in proteasome-mediated degradation of HPK1 protein in pancreatic cancer.
Specific Aim 2 : To examine the function of Fbw8-mediated HPK1 degradation in tumor growth and metastasis of pancreatic cancer.

Public Health Relevance

Proteasome-mediated Degradation of Hematopoietic Progenitor Kinase 1 in Pancreatic Cancer We recently demonstrated that HPK1 function as a novel tumor suppressor and that proteasome-mediated degradation of HPK1 protein is strongly associated with the progression from low-grade pancreatic intraepithelial neoplasia (PanIN) to invasive pancreatic cancer. In this proposal, we will examine the detailed molecular mechanisms of proteasome-mediated degradation of HPK1 protein and to examine the possible oncogenic functions of the newly identified ubiquitin-E3 ligase, Fbw8, that is responsible for HPK1 degradation in pancreatic cancer. Accomplishment of the proposed studies will reveal novel pathways of HPK1 regulation in pancreatic cancer and identify novel targets for pancreatic cancer treatment.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21CA149544-02
Application #
8220828
Study Section
Molecular Oncogenesis Study Section (MONC)
Program Officer
Woodhouse, Elizabeth
Project Start
2011-04-01
Project End
2014-03-31
Budget Start
2012-04-01
Budget End
2014-03-31
Support Year
2
Fiscal Year
2012
Total Cost
$171,825
Indirect Cost
$63,075
Name
University of Texas MD Anderson Cancer Center
Department
Pathology
Type
Other Domestic Higher Education
DUNS #
800772139
City
Houston
State
TX
Country
United States
Zip Code
77030
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