The objective of work proposed in this application is to decipher important new mechanisms that trigger the development of human cancer. Among human adenoviruses, adenovirus type 9 is unique in causing exclusively estrogen-dependent mammary tumors in experimental animals and in having E4 region-encoded open reading frame 1 (E4-ORF1), rather than E1 region-encoded E1A and E1B, as its primary oncogenic determinant. Evidence indicates that the tumorigenic potential of E4-ORF1 depends on two separate protein-interaction elements, the PDZ domain-binding motif (PBM) and Domain 2 (D2). While D2 mediates binding to several unidentified cellular proteins, the PBM interacts with a select group of cellular PDZ proteins, including the three cell polarity proteins Dlg1, ZO-2, and PATJ, as well as the PATJ paralogue MUPP1 and MAGI-1. Underscoring the link of these cellular PDZ proteins to human cancer, Dlg1, PATJ, MUPP1, and MAGI-1 are also cellular targets of high-risk human papillomavirus E6 oncoproteins and Dlg1 is a cellular target of the human T-cell leukemia virus type 1 Tax oncoprotein. Our results lead to the hypothesis that the tumorigenic potential of E4-ORF1 stems from its combined capacities to induce Dlg1- and D2 protein-dependent constitutive PI3K activation and to block both PATJ- and ZO-2-dependent apical-basal cell polarity establishment and Dlg1-dependent anterior-posterior cell polarity establishment. This hypothesis will be tested by (Aim 1) purifying, identifying, and characterizing D2-interacting proteins and determining their role in disregulated PI3K signaling, (Aim 2) investigating tumor suppressor functions for PATJ and ZO-2 in mice, and (Aim 3) determining mechanisms for E4-ORF1-induced inhibition of anterior-posterior cell polarity. The immediate benefits of completing these aims will be the elucidation of novel mechanisms leading to tumorigenic activation of the PI3K pathway and loss of cell polarity. As both defects are hallmarks of cancer cells, this information should provide important new insights into the development of a wide variety of human malignancies. In the long-term, the knowledge gained from the proposed work may aid in the development of effective new therapeutic strategies to treat and prevent human cancers.

Public Health Relevance

While cancer is a leading cause of death in developed countries, our understanding of the many different molecular mechanisms that trigger this complex disease remains somewhat limited. Two very common abnormalities of cancer cells are uncontrolled activation of the PI3K pathway and a failure to establish proper polarity. Given that we have identified a viral protein that promotes cancer by specifically causing these two defects, our research may reveal mechanisms underlying these important disease processes and thereby provide information that could be used to develop effective new therapies to treat and prevent a wide variety of human cancers.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA058541-18
Application #
8196810
Study Section
Virology - A Study Section (VIRA)
Program Officer
Daschner, Phillip J
Project Start
1993-01-01
Project End
2013-11-30
Budget Start
2011-12-01
Budget End
2012-11-30
Support Year
18
Fiscal Year
2012
Total Cost
$307,553
Indirect Cost
$107,193
Name
Baylor College of Medicine
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
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