Zerumbone Suppresses Human Colorectal Cancer Invasion and Metastasis via Modulation of FAk/PI3k/NFκB-uPA Pathway.
Cell Line, Tumor
Cell Movement
/ drug effects
Cell Proliferation
/ drug effects
Colorectal Neoplasms
/ drug therapy
Focal Adhesion Protein-Tyrosine Kinases
/ antagonists & inhibitors
Humans
NF-kappa B
/ antagonists & inhibitors
Neoplasm Invasiveness
Phosphoinositide-3 Kinase Inhibitors
/ pharmacology
Sesquiterpenes
/ pharmacology
Signal Transduction
/ drug effects
Urokinase-Type Plasminogen Activator
/ antagonists & inhibitors
Journal
Nutrition and cancer
ISSN: 1532-7914
Titre abrégé: Nutr Cancer
Pays: United States
ID NLM: 7905040
Informations de publication
Date de publication:
2019
2019
Historique:
pubmed:
18
1
2019
medline:
2
5
2020
entrez:
18
1
2019
Statut:
ppublish
Résumé
The current study explored the basic molecular mechanisms of zerumbone (ZER), an herbal compound, in inhibiting the migration and invasion of colorectal cancer (CRC) cells in vitro. Two types of CRC cells, namely HCT-116 and SW48, were treated with various concentrations of ZER (8, 16, and 24 µM) for 24, 48, and 72 h, respectively. In vitro assays were performed to determine alterations in proliferation ability, mRNA expression and protein levels, and migration and invasion potential of CRC cells. An SYBR Green-based quantitative polymerase chain reaction (PCR) was utilized to detect the gene expression of focal adhesion kinase (FAK), nuclear factor (NF)-κB, and urokinase-type plasminogen activator (uPA) followed by the evaluation of the level of proteins by western blotting. Migration and invasion potentials of HCT-116 and SW48 cells treated by ZER were examined using migration and invasion assay kits, respectively. We compared the results of all experiments with control groups, including FAK inhibitor, ZER + FAK inhibitor-treated cells, NF-β inhibitor, ZER + NF-β inhibitor, and untreated cells. The data in the present study suggest that ZER may exert its antimetastatic effects through inhibition of FAk/PI3k/NF-κB-uPA signaling pathway, thereby possibly representing a novel class of FAK inhibitors.
Identifiants
pubmed: 30650987
doi: 10.1080/01635581.2018.1540719
doi:
Substances chimiques
NF-kappa B
0
Phosphoinositide-3 Kinase Inhibitors
0
Sesquiterpenes
0
zerumbone
471-05-6
Focal Adhesion Protein-Tyrosine Kinases
EC 2.7.10.2
Urokinase-Type Plasminogen Activator
EC 3.4.21.73
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM