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Updated: May 23, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Viral lymphomas: can antivirals be used to treat cancer?
1Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY, USA. ecesarm@med.cornell.edu
Abstract:
Current knowledge suggests that EBV, KSHV and HTLV-1 contribute to lymphomagenesis by subverting the host-cell molecular signaling machinery to deregulate cell growth and survival. Some signaling pathways that are affected by these viruses are well characterized, such as the NF-kB pathway, which is activated by these three viruses to promote cellular survival by inhibiting apoptosis, thereby playing a critical role in tumorigenesis. Other pathways, such as MTOR and JAK-STAT are also likely involved in viral lymphomagenesis. This provides the opportunity to inhibit these cellular pathways using drugs developed for the treatment of other malignancies. However, since these compounds target cellular proteins, they always have the potential for toxicity. In the context of viral malignancies, we have the unique opportunity of targeting viral proteins, and developing completely specific therapies. Here we will examine the question of whether the pathobiology of EBV, KSHV and HTLV-1 will allow the use of such an approach.
Insights
Epstein-Barr virus (EBV), KSHV, and HTLV-1 drive lymphomagenesis by disrupting cell signaling. Targeting viral proteins offers a potential for specific therapies against these viral cancers.
Area of Science:
- Oncology
- Virology
- Molecular Biology
Background:
- Epstein-Barr virus (EBV), Kaposi's sarcoma-associated herpesvirus (KSHV), and Human T-lymphotropic virus type 1 (HTLV-1) are implicated in lymphomagenesis.
- These viruses subvert host-cell signaling pathways, promoting uncontrolled cell growth and survival, critical for tumor development.
Purpose of the Study:
- To investigate the potential for developing targeted therapies against viral proteins of EBV, KSHV, and HTLV-1.
- To explore whether the pathobiology of these viruses permits targeting viral proteins for cancer treatment.
Main Methods:
- Review of current knowledge on viral lymphomagenesis and affected signaling pathways (NF-kB, MTOR, JAK-STAT).
- Analysis of the feasibility of targeting viral proteins versus host-cell proteins for therapeutic intervention.
Main Results:
- Activation of the NF-kB pathway by EBV, KSHV, and HTLV-1 promotes cell survival and inhibits apoptosis, contributing to tumorigenesis.
- Other pathways like MTOR and JAK-STAT are also likely involved in viral lymphomagenesis.
Conclusions:
- Targeting host-cell signaling pathways with existing drugs is possible but carries toxicity risks.
- Targeting viral proteins offers a unique opportunity for developing highly specific therapies against EBV, KSHV, and HTLV-1-associated malignancies.
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