The complex mechanisms associated with viral oncogenesis requires a broad understanding of aspects of virology, molecular and cellular biology, and immunology. It has been stated that viruses are among the strongest carcinogens known. These viruses include hepatitis B virus, hepatitis C virus and certain human papillomaviruses. In addition, certain human herpesviruses as well as retroviruses have been associated with certain cancers. The trainers within the proposed training grant direct productive and well-funded research programs that focus on four of the five above virus groups, which include hepatitis B virus, human papillomaviruses, herpesviruses, and retroviruses. This training grant application is a competitive renewal for years 16-20 of a program to support graduate students and postdoctoral fellows who are associated with a long-standing training program in virology and immunology. The trainers associated with the proposed program have their primary academic appointments within the Departments of Microbiology and Immunology, Medicine, Pathology, or Pediatrics. Each of the trainers directs a well-funded and productive research program in areas of virology and immunology. Although the trainers and trainees are primarily associated with the Department of Microbiology and Immunology, predoctoral students are also associated with multiple interdisciplinary graduate programs that cross departmental boundaries. A strength of the program is the numerous opportunities for interactions among the trainers, which contributes to the development of a highly supportive and interactive environment in which the trainees can reach their full potential as young scientists. The breadth of the scientific interests of members of the training faculty provides a blend of research areas within aspects of virology and immunology that allows the potential for outstanding training environment. The training program is further enhanced by numerous seminars, journal clubs, symposia, and special experiences that enhance the cancer training environment. The establishment, growth, and association with the Penn State Hershey Cancer Institute have enhanced the training environment for young scientists with an interest in cancer. The research accomplishments of the faculty, their strong commitment for training, availability of excellent core support facilities, and opportunities for extensive interactions all provide a dynamic training environment for the graduate students and postdoctoral fellows within the Viruses and Cancer training program.

Public Health Relevance

Viruses are among the strongest carcinogens. The complex mechanisms associated with viral oncogenesis requires a broad understanding of aspects of virology and immunology. The trainers associated with this training grant application conduct studies with both cancer- causing and cancer-associated viruses. These well-established scientists are part of a long- standing training program that provides a dynamic training environment for young scientists.

National Institute of Health (NIH)
National Cancer Institute (NCI)
Institutional National Research Service Award (T32)
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Subcommittee G - Education (NCI)
Program Officer
Lim, Susan E
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Pennsylvania State University
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United States
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Lee, Hyunwook; Shingler, Kristin L; Organtini, Lindsey J et al. (2016) The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs. Sci Adv 2:e1501929
Organtini, Lindsey J; Lee, Hyunwook; Iketani, Sho et al. (2016) Near-Atomic Resolution Structure of a Highly Neutralizing Fab Bound to Canine Parvovirus. J Virol 90:9733-9742
Cui, Xiuji; Clark, Daniel N; Liu, Kuancheng et al. (2016) Viral DNA-Dependent Induction of Innate Immune Response to Hepatitis B Virus in Immortalized Mouse Hepatocytes. J Virol 90:486-96
Sei, Janet J; Haskett, Scott; Kaminsky, Lauren W et al. (2015) Peptide-MHC-I from Endogenous Antigen Outnumber Those from Exogenous Antigen, Irrespective of APC Phenotype or Activation. PLoS Pathog 11:e1004941
Clark, Daniel N; Hu, Jianming (2015) Hepatitis B virus reverse transcriptase - Target of current antiviral therapy and future drug development. Antiviral Res 123:132-7
Clark, Daniel N; Hu, Jianming (2015) Unveiling the roles of HBV polymerase for new antiviral strategies. Future Virol 10:283-295
Shingler, Kristin L; Cifuente, Javier O; Ashley, Robert E et al. (2015) The enterovirus 71 procapsid binds neutralizing antibodies and rescues virus infection in vitro. J Virol 89:1900-8
Kaminsky, Lauren W; Sei, Janet J; Parekh, Nikhil J et al. (2015) Redundant Function of Plasmacytoid and Conventional Dendritic Cells Is Required To Survive a Natural Virus Infection. J Virol 89:9974-85
Goh, Boon Chong; Perilla, Juan R; England, Matthew R et al. (2015) Atomic Modeling of an Immature Retroviral Lattice Using Molecular Dynamics and Mutagenesis. Structure 23:1414-25
Cui, Xiuji; McAllister, Rebecca; Boregowda, Rajeev et al. (2015) Does Tyrosyl DNA Phosphodiesterase-2 Play a Role in Hepatitis B Virus Genome Repair? PLoS One 10:e0128401

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