Extracellular Vesicles Induce Mesenchymal Transition and Therapeutic Resistance in Glioblastomas through NF‐κB/STAT3 Signaling
Author(s) -
Schweiger Markus W.,
Li Mao,
Giovanazzi Alberta,
Fleming Renata L.,
Tabet Elie I.,
Nakano Ichiro,
Würdinger Thomas,
Chiocca Ennio Antonio,
Tian Tian,
Tannous Bakhos A.
Publication year - 2020
Publication title -
advanced biosystems
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.153
H-Index - 18
ISSN - 2366-7478
DOI - 10.1002/adbi.201900312
Subject(s) - mesenchymal stem cell , stat3 , cancer research , glioma , epithelial–mesenchymal transition , stat protein , biology , transcription factor , signal transduction , activator (genetics) , microbiology and biotechnology , transition (genetics) , gene , genetics
Glioblastoma (GBM) is the most common primary malignant brain tumor and despite optimal treatment, long‐term survival remains uncommon. GBM can be roughly divided into three different molecular subtypes, each varying in aggressiveness and treatment resistance. Recent evidence shows plasticity between these subtypes in which the proneural (PN) glioma stem‐like cells (GSCs) undergo transition into the more aggressive mesenchymal (MES) subtype, leading to therapeutic resistance. Extracellular vesicles (EVs) are membranous structures secreted by nearly every cell and are shown to play a key role in GBM progression by acting as multifunctional signaling complexes. Here, it is shown that EVs derived from MES cells educate PN cells to increase stemness, invasiveness, cell proliferation, migration potential, aggressiveness, and therapeutic resistance by inducing mesenchymal transition through nuclear factor‐κB/signal transducer and activator of transcription 3 signaling. The findings could potentially help explore new treatment strategies for GBM and indicate that EVs may also play a role in mesenchymal transition of different tumor types.
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