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Cited 46 time in webofscience Cited 48 time in scopus
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VEGF-C mediates RhoGDI2-induced gastric cancer cell metastasis and cisplatin resistance

Authors
Cho, Hee JunKim, In-KyuPark, Sun-MiBaek, Kyoung EunNam, In-KooPark, Seung-HoRyu, Ki-JunChoi, JungilRyu, JinhyunHong, Soon-ChanJeong, Sang-HoLee, Young-JoonKo, Gyung-HyuckKim, Jae WonLee, Chang WonKang, Sang SooYoo, Jiyun
Issue Date
Oct-2014
Publisher
John Wiley & Sons Inc.
Keywords
RhoGDI2; VEGF-C; gastric cancer; metastasis; chemoresistance
Citation
International Journal of Cancer, v.135, no.7, pp 1553 - 1563
Pages
11
Indexed
SCI
SCIE
SCOPUS
Journal Title
International Journal of Cancer
Volume
135
Number
7
Start Page
1553
End Page
1563
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/18717
DOI
10.1002/ijc.28801
ISSN
0020-7136
1097-0215
Abstract
Rho GDP dissociation inhibitor 2 (RhoGDI2) expression is correlated with tumor growth, metastasis and chemoresistance in gastric cancer. However, the mechanisms by which RhoGDI2 promotes tumor cell survival and metastasis remain unclear. In this study, we clearly demonstrate that RhoGDI2 upregulates VEGF-C expression and RhoGDI2 expression is positively correlated with VEGF-C expression in human gastric tumor tissues as well as parental gastric cancer cell lines. VEGF-C depletion suppressed RhoGDI2-induced gastric cancer metastasis and sensitized RhoGDI2-overexpressing cells to cisplatin-induced apoptosis in vitro and in vivo. Secreted VEGF-C enhanced gastric cancer cell invasion and conferred cisplatin resistance to RhoGDI2-overexpressing cells. We also show that RhoGDI2 positively regulates Rac1 activity in gastric cancer cells. Inhibition of Rac1 expression suppressed RhoGDI2-induced VEGF-C expression, and this inhibition was associated with decreased invasiveness and increased sensitivity to cisplatin in RhoGDI2-overexpressing cells. Our results indicate that RhoGDI2 might be a potential therapeutic target for simultaneously reducing metastasis risk and enhancing chemotherapy efficacy in gastric cancer.
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