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Frizzled 4 Regulates Stemness and Invasiveness of Migrating Glioma Cells Established by Serial Intracranial Transplantation

Authors
Jin, XunJeon, Hee-YoungJoo, Kyeung MinKim, Jun-KyumJin, JuyounKim, Sung HakKang, Bong GuBeck, SamuelLee, Se JeongKim, Joong KyuPark, Ae-KyungPark, Woong-YangChoi, Yun-JaieNam, Do-HyunKim, Hyunggee
Issue Date
15-4월-2011
Publisher
AMER ASSOC CANCER RESEARCH
Citation
CANCER RESEARCH, v.71, no.8, pp.3066 - 3075
Indexed
SCIE
SCOPUS
Journal Title
CANCER RESEARCH
Volume
71
Number
8
Start Page
3066
End Page
3075
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/112654
DOI
10.1158/0008-5472.CAN-10-1495
ISSN
0008-5472
Abstract
One of the most detrimental hallmarks of glioblastoma multiforme (GBM) is cellular invasiveness, which is considered a potential cause of tumor recurrence. Infiltrated GBM cells are difficult to completely eradicate surgically and with local therapeutic modalities. Although much effort has focused on understanding the various mechanisms controlling GBM invasiveness, its nature remains poorly understood. In this study, we established highly serial intracranial transplantation. U87R4 cells were highly invasive and displayed stem cell-like properties, as compared to noninvasive but proliferative U87L4 cells. Microarray analysis during serial transplantation revealed that apoptosis-inducing genes (caspase3 and PDCD4) were downregulated whereas several cancer stem cell-relevant genes [Frizzled 4 (FZD4) and CD44] were upregulated in more invasive cells. U87R4 cells were resistant to anticancer drug-induced cell death, partly due to downregulation of caspase3 and PDCD4, and they retained activated Wnt/beta-catenin signaling due to upregulation of Frizzled 4, which was sufficient to control neurosphere formation. We also found that FZD4 promoted expression of the epithelial to mesenchymal transition regulator SNAI1, along with acquisition of a mesenchymal phenotype. Taken together, our results argue that Frizzled 4 is a member of the Wnt signaling family that governs both stemness and invasiveness of glioma stem cells, and that it may be a major cause of GBM recurrence and poor prognosis. Cancer Res; 71(8); 3066-75. (C) 2011 AACR.
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