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Silencing of Glucose-Regulated Protein 78 (GRP78) Enhances Cell Migration Through the Upregulation of Vimentin in Hepatocellular Carcinoma Cells
- Source :
- Annals of Surgical Oncology. 19:572-579
- Publication Year :
- 2011
- Publisher :
- Springer Science and Business Media LLC, 2011.
-
Abstract
- Glucose-regulated protein 78 (GRP78) plays an important role in embryonic development and cancer progression. However, there is little information regarding the regulation of GRP78 in hepatocellular carcinoma (HCC) metastasis.We used RNA silencing and cDNA expression vectors to manipulate target gene expression in HCC cells. The transwell migration assay and xCelligence biosensor system were applied to determine the proliferatory and migratory ability of the HCC cells.In this study, we found that GRP78 silencing enhanced cell migration in both HepJ5 and Mahlavu cells. Overexpressed GRP78 in skHep1 cells suppressed the migratory ability. In the insight mechanism dissection for GRP78-mediated cancer migration, we found that downregulation of GRP78 caused the increase of vimentin expression on HCC cells. Suppressed vimentin expression also decreased the migratory ability on HCC, indicating that vimentin expression levels modulated the cell migratory ability.We found that silencing GRP78 in HCC cells may enhance cell migration through the increase of vimentin expression.
- Subjects :
- Carcinoma, Hepatocellular
Epithelial-Mesenchymal Transition
Glucose-regulated protein
Genetic Vectors
Down-Regulation
Vimentin
Metastasis
Downregulation and upregulation
Cell Movement
Cell Line, Tumor
medicine
Carcinoma
Humans
Epithelial–mesenchymal transition
Endoplasmic Reticulum Chaperone BiP
Heat-Shock Proteins
Cell Proliferation
biology
business.industry
Liver Neoplasms
Cell migration
medicine.disease
digestive system diseases
Up-Regulation
Oncology
Hepatocellular carcinoma
biology.protein
Cancer research
RNA Interference
Surgery
business
Subjects
Details
- ISSN :
- 15344681 and 10689265
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Annals of Surgical Oncology
- Accession number :
- edsair.doi.dedup.....a64a770791f4e4889858f4dcbb03b6e6
- Full Text :
- https://doi.org/10.1245/s10434-011-2055-y