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Updated: May 28, 2026

Isolation and Flow Cytometric Analysis of Glioma-infiltrating Peripheral Blood Mononuclear Cells
Published on: November 28, 2015
Evolving evidence implicates cytomegalovirus as a promoter of malignant glioma pathogenesis
1California Pacific Medical Center Research Institute, 475 Brannan Street, San Francisco, CA, 94114, USA. charles.cobbs@gmail.com.
Abstract:
Human cytomegalovirus (HCMV) was first reported to be strongly associated with human malignant gliomas in 2002. HCMV is a herpesvirus that causes congenital brain infection and multi-organ disease in immumocompromised individuals. Malignant gliomas are the most common and aggressive adult brain tumors and glioblastoma multiforme (GBM), the highest grade glioma, is associated with a life expectancy of less than two years. HCMV gene products encode for multiple proteins that can promote the various signaling pathways critical to tumor growth, including those involved in mitogenesis, mutagenesis, apoptosis, inflammation, angiogenesis, invasion and immuno-evasion. Several groups have now demonstrated that human malignant gliomas are universally infected with HCMV and express gene products that can promote key signaling pathways in glioma pathogenesis. In this review I discuss specific HCMV gene products that we and others have recently found to be expressed in GBM in vivo, including the HCMV IE1, US28, gB and IL-10 proteins. The roles these HCMV gene products play in dysregulating key pathways in glioma biology, including the PDGFR, AKT, STAT3, and monocyte/microglia function are discussed. Finally, I review emerging human clinical trials for GBM based on anti-HCMV strategies.
Insights
Human cytomegalovirus (HCMV) drives malignant glioma growth by expressing proteins that promote tumor progression. Targeting HCMV offers a promising new strategy for treating glioblastoma multiforme (GBM).
Area of Science:
- Oncology
- Virology
- Neuroscience
Background:
- Malignant gliomas, particularly glioblastoma multiforme (GBM), are aggressive brain tumors with poor prognoses.
- Human cytomegalovirus (HCMV) infection is increasingly recognized as a significant factor in glioma development and progression.
- HCMV is a herpesvirus known to cause congenital infections and disease in immunocompromised individuals.
Purpose of the Study:
- To review the role of HCMV gene products in promoting glioma pathogenesis.
- To discuss specific HCMV proteins expressed in GBM and their impact on critical signaling pathways.
- To explore emerging anti-HCMV therapeutic strategies for GBM.
Main Methods:
- Review of existing literature and research findings on HCMV and malignant gliomas.
- Analysis of specific HCMV gene products (IE1, US28, gB, IL-10) found in GBM.
- Discussion of HCMV's influence on key signaling pathways (PDGFR, AKT, STAT3) and immune cells.
Main Results:
- HCMV is universally present in human malignant gliomas.
- HCMV proteins contribute to tumor growth by influencing mitogenesis, mutagenesis, apoptosis, inflammation, angiogenesis, invasion, and immuno-evasion.
- HCMV gene products dysregulate essential glioma pathways, including PDGFR, AKT, and STAT3 signaling, and affect monocyte/microglia function.
Conclusions:
- HCMV plays a critical role in the pathogenesis of malignant gliomas.
- Targeting HCMV offers a novel therapeutic avenue for GBM treatment.
- Emerging clinical trials are investigating anti-HCMV strategies for GBM.
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