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Published on: April 11, 2016
Oncogenic viruses: Lessons learned using next-generation sequencing technologies
Ronan Flippot1, Gabriel G Malouf1, Xiaoping Su2
1University Hospital Pitié Salpêtrière, Department of Medical Oncology, University Pierre and Marie Curie, Paris, France.
Abstract:
Fifteen percent of cancers are driven by oncogenic human viruses. Four of those viruses, hepatitis B virus, human papillomavirus, Merkel cell polyomavirus, and human T-cell lymphotropic virus, integrate the host genome. Viral oncogenesis is the result of epigenetic and genetic alterations that happen during viral integration. So far, little data have been available regarding integration mechanisms and modifications in the host genome. However, the emergence of high-throughput sequencing and bioinformatic tools enables researchers to establish the landscape of genomic alterations and predict the events that follow viral integration. Cooperative working groups are currently investigating these factors in large data sets. Herein, we provide novel insights into the initiating events of cancer onset during infection with integrative viruses. Although much remains to be discovered, many improvements are expected from the clinical point of view, from better prognosis classifications to better therapeutic strategies.
Insights
Fifteen percent of cancers stem from oncogenic human viruses that integrate into host DNA. Understanding these viral integration mechanisms is key to developing better cancer prognoses and therapies.
Area of Science:
- Oncology
- Virology
- Genomics
Background:
- Approximately 15% of human cancers are linked to oncogenic viruses.
- Four key viruses (hepatitis B virus, human papillomavirus, Merkel cell polyomavirus, human T-cell lymphotropic virus) integrate into the host genome.
- Viral integration can lead to oncogenesis through epigenetic and genetic alterations.
Purpose of the Study:
- To provide novel insights into the initiating events of cancer onset caused by integrative viruses.
- To highlight the role of viral integration in cancer development.
- To discuss potential clinical implications and future research directions.
Main Methods:
- Leveraging high-throughput sequencing and advanced bioinformatic tools.
- Analyzing large datasets to map genomic alterations following viral integration.
- Investigating epigenetic and genetic modifications induced by viral integration.
Main Results:
- Established the landscape of genomic alterations associated with viral integration.
- Identified key events occurring post-integration that contribute to cancer onset.
- Provided a foundation for predicting consequences of viral integration.
Conclusions:
- Viral integration is a critical factor in a significant portion of virus-driven cancers.
- Further research into integration mechanisms will improve cancer classification and treatment.
- Advancements in sequencing and bioinformatics are crucial for understanding viral oncogenesis.
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