Understanding the Oncogenesis of Human Herpesviruses through Their Critical Comparisons

A special issue of Viruses (ISSN 1999-4915). This special issue belongs to the section "Human Virology and Viral Diseases".

Deadline for manuscript submissions: 31 August 2024 | Viewed by 485

Special Issue Editors


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Guest Editor
School of Medicine, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan
Interests: oncogenic viruses

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Guest Editor
McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI 53705, USA
Interests: EBV-associated tumors
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Special Issue Information

Dear Colleagues,

Two human herpesviruses, Epstein–Barr virus (EBV) and Kaposi’s sarcoma herpesvirus (KSHV), cause lymphomas, carcinomas, and sarcomas in people. These viruses were discovered in 1964 and 1994 and have been studied intensively since then. We are assembling, under the auspices of Viruses, a collection of reviews to address these studies creatively. We propose to compare and contrast how these two tumor viruses together contribute to oncogenesis. We plan for each review to cover a given topic for both EBV and KSHV, a creative combination, which is yet to be carried out systematically.

We envision three topics to consider the facets of the life-cycles of EBV and KSHV that underpin their normal infections in people. These topics provide a background for considering the rare events that lead to tumorigenesis. These are as follows:

  1. What are the latent reservoirs of EBV and KSHV?
  2. How do EBV and KSHV persist in vivo and avoid their productive infections killing cells that may evolve into tumors?
  3. How do EBV and KSHV benefit from their plasmid replicons?

With these topics as a foundation, we envision five more to describe oncogenesis mediated by EBV and KSHV. They include the following:

  1. How do cells infected with EBV and KSHV escape being killed by their host's immune responses?
  2. How do EBV and KSHV suppress tumor suppressors?
  3. How do EBV and KSHV mediate lymphomagenesis in BL, DLBCL, and PEL?
  4. How do EBV and KSHV mediate the development of carcinomas and sarcomas?
  5. How will vaccines protect against herpesvirus oncogenesis?

We expect that these eight topics will illuminate the oncogenesis of both EBV and KSHV by comparing and contrasting their life-cycles and their transforming properties. Scientists or teams with expertise in both of these human tumor viruses might consider contributing to this ensemble, reflecting 90 years of combined research on EBV and KSHV. 

Dr. Ya-Fang Chiu
Prof. Dr. Bill Sugden
Guest Editors

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