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Specificity Protein 1 Expression Contributes to Bcl-w-Induced Aggressiveness in Glioblastoma Multiformeopen access

Authors
Lee, Woo SangKwon, JunhyeYun, Dong HoLee, Young NamWoo, Eun YoungPark, Myung-JinLee, Jae-SeonHan, Young-HoonBae, In Hwa
Issue Date
Jan-2014
Publisher
KOREAN SOC MOLECULAR & CELLULAR BIOLOGY
Keywords
aggressiveness; Bcl-w; glioblastoma multiforme; glioma stem cell markers; invasion; Sp1
Citation
MOLECULES AND CELLS, v.37, no.1, pp 17 - 23
Pages
7
Journal Title
MOLECULES AND CELLS
Volume
37
Number
1
Start Page
17
End Page
23
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/11027
DOI
10.14348/molcells.2014.2161
ISSN
1016-8478
0219-1032
Abstract
We already had reported that Bcl-w promotes invasion or migration in gastric cancer cells and glioblastoma multiforme (GBM) by activating matrix metalloproteinase-2 (MMP-2) via specificity protein 1 (Sp1) or beta-cateinin, respectively. High expression of Bcl-w also has been reported in GBM which is the most common malignant brain tumor and exhibits aggressive and invasive behavior. These reports propose that Bcl-w-induced signaling is strongly associated with aggressive characteristic of GBM. We demonstrated that Sp1 protein or mRNA expression is induced by Bcl-w using Western blotting or RT-PCR, respectively, and markedly elevated in high-grade glioma specimens compared with low-grade glioma tissues using tissue array. However, relationship between Bcl-w-related signaling and aggressive characteristic of GBM is poorly characterized. This study suggested that Bcl-w-induced Sp1 activation promoted expression of glioma stem-like cell markers, such as Musashi, Nanog, Oct4 and sox-2, as well as neurosphere formation and invasiveness, using western blotting, neurosphere formation assay, or invasion assay, culminating in their aggressive behavior. Therefore, Bcl-w-induced Sp1 activation is proposed as a putative marker for aggressiveness of GBM.
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