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Cited 105 time in webofscience Cited 111 time in scopus
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CHI3L1 (YKL-40) is expressed in human gliomas and regulates the invasion, growth and survival of glioma cells

Authors
Ku, Bo MiLee, Yeon KyungRyu, JinhyunJeong, Joo YeonChoi, JungilEun, Keyoung MiShin, Hye YoungKim, Dong GyuHwang, Eun MiYoo, Jae ChealPark, Jae-YongRoh, Gu SeobKim, Hyun JoonCho, Gyeong JaeChoi, Wan SungPaek, Sun HaKang, Sang Soo
Issue Date
Mar-2011
Publisher
John Wiley & Sons Inc.
Keywords
CHI3L1; glioblastoma; local invasion; malignant transformation
Citation
International Journal of Cancer, v.128, no.6, pp 1316 - 1326
Pages
11
Indexed
SCI
SCIE
SCOPUS
Journal Title
International Journal of Cancer
Volume
128
Number
6
Start Page
1316
End Page
1326
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/23809
DOI
10.1002/ijc.25466
ISSN
0020-7136
1097-0215
Abstract
Chitinase 3-like 1 (CHI3L1) is a secreted glycoprotein that has pleiotropic activity in aggressive cancers. In our study, we examined the expression and function of CHI3L1 in glioma cells. CHI3L1 was highly expressed in human glioma tissue, whereas its expression in normal brain tissue was very low. CHI3L1 suppression by shRNA reduced glioma cell invasion, anchorage-independent growth and increased cell death triggered by several anticancer drugs, including cisplatin, etoposide and doxorubicin, whereas CHI3L1 overexpression had the opposite effect in glioma cells. Because the invasive nature of glioma cells plays a critical role in the high morbidity of glioma, we have further defined the role of CHI3L1 in the process of glioma invasion. Downregulation of CHI3L1 results in decreased cell-matrix adhesion and causes a marked increase in stress fiber formation and cell size with fewer cellular processes. Furthermore, the expression and activity of matrix metalloproteinase-2 was also decreased in glioma cells in which CHI3L1 was knocked down. Taken together, these results suggest that CHI3L1 plays an important role in the regulation of malignant transformation and local invasiveness in gliomas. Thus, targeting the CHI3L1 molecule may be a potential therapeutic molecular target for gliomas.
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