Overcoming therapeutic resistance in oncolytic herpes virotherapy by targeting IGF2BP3-induced NETosis in malignant glioma.
Weiwei DaiRuotong TianLiubing YuShasha BianYuling ChenBowen YinYuxuan LuanSiqi ChenZhuoyang FanRucheng YanXin PanYingyong HouRong LiJuxiang ChenMinfeng ShuPublished in: Nature communications (2024)
Oncolytic virotherapy holds promise for cancer treatment, but the factors determining its oncolytic activity remain unclear. Neutrophil extracellular traps (NETs) are associated with cancer progression, yet their formation mechanism and role in oncolytic virotherapy remain elusive. In this study, we demonstrate that, in glioma, upregulation of IGF2BP3 enhances the expression of E3 ubiquitin protein ligase MIB1, promoting FTO degradation via the ubiquitin-proteasome pathway. This results in increased m6A-mediated CSF3 release and NET formation. Oncolytic herpes simplex virus (oHSV) stimulates IGF2BP3-induced NET formation in malignant glioma. In glioma models in female mice, a BET inhibitor enhances the oncolytic activity of oHSV by impeding IGF2BP3-induced NETosis, reinforcing virus replication through BRD4 recruitment with the CDK9/RPB-1 complex to HSV gene promoters. Our findings unveil the regulation of m6A-mediated NET formation, highlight oncolytic virus-induced NETosis as a critical checkpoint hindering oncolytic potential, and propose targeting NETosis as a strategy to overcome resistance in oncolytic virotherapy.
Keyphrases
- high glucose
- diabetic rats
- herpes simplex virus
- binding protein
- poor prognosis
- small molecule
- drug induced
- gene expression
- type diabetes
- endothelial cells
- machine learning
- dna damage
- growth hormone
- oxidative stress
- risk assessment
- dna methylation
- skeletal muscle
- insulin resistance
- drug delivery
- genome wide
- long non coding rna
- papillary thyroid
- amino acid