Oncolytic HSV-1–Mediated JAG1 Blockade Induces Glioma Senescence-Associated Secretory Phenotype to Increase Macrophage Activation and Cetuximab-Mediated Senolysis

Leveraging JAG1 antagonism in the context of oncolytic virotherapy rewires macrophage polarization within the tumor microenvironment, which has wide implications for sensitizing tumors to antibodies, senolytic agents, and BiTE therapies.

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Publication Details

Journal
Cancer Research
Published
2025-12-18
DOI
https://doi.org/10.1158/0008-5472.can-25-1402
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
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article

Oncolytic HSV-1–Mediated JAG1 Blockade Induces Glioma Senescence-Associated Secretory Phenotype to Increase Macrophage Activation and Cetuximab-Mediated Senolysis

Tae Jin Lee, Ashok Sharma, Marco Orecchioni, Karina Vázquez-Arreguín et al.
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Virus-based gene therapy research
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Oncolytic HSV-1–Mediated JAG1 Blockade Induces Glioma Senescence-Associated Secretory Phenotype to Increase Macrophage Activation and Cetuximab-Mediated Senolysis

Tae Jin Lee, Ashok Sharma, Marco Orecchioni, Karina Vázquez-Arreguín, Kimberly Rivera-Caraballo, Sara A. Murphy, Kimya Jones, Ravindra B Kolhe, Balveen Kaur, Upasana Sahu, Rafał Pacholczyk, Shilpa Sharma, Bangxing Hong, Amritanshu Sinha, Kailash Vemuri
article en

Abstract

Leveraging JAG1 antagonism in the context of oncolytic virotherapy rewires macrophage polarization within the tumor microenvironment, which has wide implications for sensitizing tumors to antibodies, senolytic agents, and BiTE therapies.

Cancer ResearchVol. 86(5)
The University of Texas MD Anderson Cancer Center (US), Augusta University (US), Augusta University Health (US), University of Maine at Augusta (US)
Openalex Percentile: Top 57%
Virus-based gene therapy research
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