TLR9 is critical for glioma stem cell maintenance and targeting

Understanding supports for cancer stem-like cells in malignant glioma may suggest therapeutic strategies for their elimination. Here, we show that the Toll-like receptor TLR9 is elevated in glioma stem-like cells (GSC) in which it contributes to glioma growth. TLR9 overexpression is regulated by STA...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2014-09, Vol.74 (18), p.5218-5228
Hauptverfasser: Herrmann, Andreas, Cherryholmes, Gregory, Schroeder, Anne, Phallen, Jillian, Alizadeh, Darya, Xin, Hong, Wang, Tianyi, Lee, Heehyoung, Lahtz, Christoph, Swiderski, Piotr, Armstrong, Brian, Kowolik, Claudia, Gallia, Gary L, Lim, Michael, Brown, Christine, Badie, Behnam, Forman, Stephen, Kortylewski, Marcin, Jove, Richard, Yu, Hua
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Understanding supports for cancer stem-like cells in malignant glioma may suggest therapeutic strategies for their elimination. Here, we show that the Toll-like receptor TLR9 is elevated in glioma stem-like cells (GSC) in which it contributes to glioma growth. TLR9 overexpression is regulated by STAT3, which is required for GSC maintenance. Stimulation of TLR9 with a CpG ligand (CpG ODN) promoted GSC growth, whereas silencing TLR9 expression abrogated GSC development. CpG-ODN treatment induced Frizzled4-dependent activation of JAK2, thereby activating STAT3. Targeted delivery of siRNA into GSC was achieved via TLR9 using CpG-siRNA conjugates. Through local or systemic treatment, administration of CpG-Stat3 siRNA to silence STAT3 in vivo reduced GSC along with glioma growth. Our findings identify TLR9 as a functional marker for GSC and a target for the delivery of efficacious therapeutics for glioma treatment. Cancer Res; 74(18); 5218-28. ©2014 AACR.
ISSN:0008-5472
1538-7445
DOI:10.1158/0008-5472.CAN-14-1151