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PMID: 23153558 Published · ppublish English Journal Article

Gallic acid inhibits gastric cancer cells metastasis and invasive growth via increased expression of RhoB, downregulation of AKT/small GTPase signals and inhibition of NF-κB activity.

Toxicology and applied pharmacology ·Vol. 266 ·No. 1 ·2013-01-01 ·Pages 76-85

Ho HH, Chang CS, Ho WC, Liao SY, Lin WL, Wang CJ

Abstract

Our previous study demonstrated the therapeutic potential of gallic acid (GA) for controlling tumor metastasis through its inhibitory effect on the motility of AGS cells. A noteworthy finding in our previous experiment was increased RhoB expression in GA-treated cells. The aim of this study was to evaluate the role of RhoB expression on the inhibitory effects of GA on AGS cells. By applying the transfection of RhoB siRNA into AGS cells and an animal model, we tested the effect of GA on inhibition of tumor growth and RhoB expression. The results confirmed that RhoB-siRNA transfection induced GA to inhibit AGS cells' invasive growth involving blocking the AKT/small GTPase signals pathway and inhibition of NF-κB activity. Finally, we evaluated the effect of GA on AGS cell metastasis by colonization of tumor cells in nude mice. It showed GA inhibited tumor cells growth via the expression of RhoB. These data support the inhibitory effect of GA which was shown to inhibit gastric cancer cell metastasis and invasive growth via increased expression of RhoB, downregulation of AKT/small GTPase signals and inhibition of NF-κB activity. Thus, GA might be a potential agent in treating gastric cancer.

MeSH Terms
Animals Cell Line, Tumor Down-Regulation/drug effects,physiology GTP Phosphohydrolases/metabolism Gallic Acid/pharmacology,therapeutic use Gene Expression Regulation, Neoplastic Humans Male Mice Mice, Inbred BALB C Mice, Nude NF-kappa B/antagonists & inhibitors,metabolism Neoplasm Invasiveness/pathology,prevention & control Proto-Oncogene Proteins c-akt/metabolism Signal Transduction/drug effects,physiology Stomach Neoplasms/metabolism rhoB GTP-Binding Protein/biosynthesis
Chemicals
NF-kappa B Gallic Acid Proto-Oncogene Proteins c-akt GTP Phosphohydrolases rhoB GTP-Binding Protein
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Ho Hsieh-Hsun
Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung 402, Taiwan.
Chang Chi-Sen
Ho Wei-Chi
Liao Sheng-You
Lin Wea-Lung
Wang Chau-Jong
Article Info
Journal
Toxicology and applied pharmacology
Abbr.
Toxicol Appl Pharmacol
ISSN
1096-0333
Published
2013-01-01
Epub
2012-00-13
Pages
76-85
Language
English
Region
United States
NLM ID
0416575
Subset
IM
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