The theme of this program project grant is the molecular biology and genetics of viral carcinogenesis and the relationship of the processes involved in viral carcinogenesis and replication to normal cellular processes. Temin, Risser, and Panganiban study avian and murine retroviruses (spleen necrosis virus (SNV) and murine leukemia virus (MLV)); Risser also studies human immunodeficiency virus (HIV); Mertz studies simian virus 40 (SV40), a monkey papova virus; and Sugden studies Epstein-Barr virus (EBV), a human herpes virus. Temin plans studies that will enhance the ability to construct retroviruses with different properties and will use this ability to study retrovirus replication, variation, and evolution and the genetic mechanisms of oncogenesis. Mertz's objective is to understand at the molecular level the mechanisms by which the expression of the late genes of SV40 are regulated and the ways in which the virus-encoded large T antigen affects that regulation. Panganiban's research will examine the post-transcriptional expression and post-translational regulation of the retroviral pol gene open reading frame and the activity of one of its products, the int protein, as well as examining the function of the retrovirus env gene product. Risser will study the role of envelope protein expression in the retrovirus life cycle and pathogenesis. His research group will determine the role of regions of the envelope gene in virus function, identify and characterize the viral and cellular determinants of viral host range and cytopathology, and determine the pathologic consequences of high level viral env gene expression in cells and organisms. Sugden's research centers on the identification and characterization of those genetic elements of Epstein-Barr virus (EBV) required for efficient immortalization of human B-lymphocytes and for latent infection of human epithelial cells.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA022443-12
Application #
3092987
Study Section
Cancer Special Program Advisory Committee (CAK)
Project Start
1978-04-01
Project End
1993-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
12
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Meyers, Jordan M; Grace, Miranda; Uberoi, Aayushi et al. (2018) Inhibition of TGF-? and NOTCH Signaling by Cutaneous Papillomaviruses. Front Microbiol 9:389
Uberoi, Aayushi; Yoshida, Satoshi; Lambert, Paul F (2018) Development of an in vivo infection model to study Mouse papillomavirus-1 (MmuPV1). J Virol Methods 253:11-17
Djavadian, Reza; Hayes, Mitchell; Johannsen, Eric (2018) CAGE-seq analysis of Epstein-Barr virus lytic gene transcription: 3 kinetic classes from 2 mechanisms. PLoS Pathog 14:e1007114
Chakravorty, Adityarup; Sugden, Bill (2018) Long-distance communication: Looping of human papillomavirus genomes regulates expression of viral oncogenes. PLoS Biol 16:e3000062
Chiu, Ya-Fang; Sugden, Bill (2018) Plasmid Partitioning by Human Tumor Viruses. J Virol 92:
Shin, Myeong-Kyun; Payne, Susan N; Bilger, Andrea et al. (2018) Activating Mutations in Pik3caContribute to Anal Carcinogenesis in the Presence or Absence of HPV-16 Oncogenes. Clin Cancer Res :
Hoebe, Eveline; Wille, Coral; Hagemeier, Stacy et al. (2018) Epstein-Barr Virus Gene BARF1 Expression is Regulated by the Epithelial Differentiation Factor ?Np63? in Undifferentiated Nasopharyngeal Carcinoma. Cancers (Basel) 10:
Nyman, Patrick E; Buehler, Darya; Lambert, Paul F (2018) Loss of Function of Canonical Notch Signaling Drives Head and Neck Carcinogenesis. Clin Cancer Res 24:6308-6318
Weng, Chao; Lee, Denis; Gelbmann, Christopher B et al. (2018) Human Cytomegalovirus Productively Replicates In Vitro in Undifferentiated Oral Epithelial Cells. J Virol 92:
Bristol, Jillian A; Djavadian, Reza; Albright, Emily R et al. (2018) A cancer-associated Epstein-Barr virus BZLF1 promoter variant enhances lytic infection. PLoS Pathog 14:e1007179

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