Exosomal Lnc-DLK1-35 reprograms microglia into a pro-tumorigenic phenotype via a non-canonical cytokine signature to promote glioblastoma progression and chemoresistance

Exosomal Lnc-DLK1-35 reprograms cultured microglia cells into a pro-tumorigenic state via a non-canonical cytokine signature, driving TMZ resistance and invasion. Targeting this axis disrupts microglia-GBM communication, revealing a novel therapeutic strategy.

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Publication Details

Journal
Folia Histochemica et Cytobiologica
Published
2026-03-11
DOI
https://doi.org/10.5603/fhc.109684
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
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article

Exosomal Lnc-DLK1-35 reprograms microglia into a pro-tumorigenic phenotype via a non-canonical cytokine signature to promote glioblastoma progression and chemoresistance

Xuan Zheng, Yongliang Liu, Jianxiong Guo, Ye Li et al.
Folia Histochemica et Cytobiologica
Neuroinflammation and Neurodegeneration Mechanisms
article

Exosomal Lnc-DLK1-35 reprograms microglia into a pro-tumorigenic phenotype via a non-canonical cytokine signature to promote glioblastoma progression and chemoresistance

Xuan Zheng, Yongliang Liu, Jianxiong Guo, Ye Li, Di Li, Yuhui Li, Jingwu Li, Zhuo Wang, Yang Wang
article en

Abstract

Exosomal Lnc-DLK1-35 reprograms cultured microglia cells into a pro-tumorigenic state via a non-canonical cytokine signature, driving TMZ resistance and invasion. Targeting this axis disrupts microglia-GBM communication, revealing a novel therapeutic strategy.

Folia Histochemica et Cytobiologica
Hospital of Hebei Province (CN), Tangshan People's Hospital (CN), TED University (TR)
Good health and well-being
Openalex Percentile: Top 41%
Neuroinflammation and Neurodegeneration Mechanisms
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