Abstract | PURPOSE: METHODS: Wound-healing assay and transwell assay were performed to study whether GGTase-I and Ras-like GTPase B (RalB) have effect on glioma cell migration and invasion. RESULTS: We found that knockdown of GGTase-I or RalB both significantly decreased the migratory and invasive abilities of glioma cells. GGTase-I down-regulation suppressed RalB membrane association. Moreover, down-regulation of RalB partially abolished the effect of GGTβ over-expression-induced glioma cell migration and invasion increase. CONCLUSIONS: These findings suggest that RalB might be one of the targets for facilitating the invasive phenotype of malignant gliomas induced by GGTase-I.
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Authors | X Song, L Hua, Y Xu, Z Fang, Y Wang, J Gao, Q Shi, X Zhou, R Yu |
Journal | Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
(Clin Transl Oncol)
Vol. 17
Issue 6
Pg. 477-85
(Jun 2015)
ISSN: 1699-3055 [Electronic] Italy |
PMID | 25573158
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- RNA, Small Interfering
- Ralb protein, human
- Alkyl and Aryl Transferases
- geranylgeranyltransferase type-I
- ral GTP-Binding Proteins
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Topics |
- Alkyl and Aryl Transferases
(metabolism)
- Blotting, Western
- Cell Line, Tumor
- Cell Movement
(physiology)
- Glioma
(pathology)
- Humans
- Neoplasm Invasiveness
(pathology)
- RNA, Small Interfering
- Transfection
- ral GTP-Binding Proteins
(metabolism)
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