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Zerumbone Suppresses Human Colorectal Cancer Invasion and Metastasis via Modulation of FAk/PI3k/NFκB-uPA Pathway.
Hosseini, Narges; Khoshnazar, Amineh; Saidijam, Massoud; Azizi Jalilian, Farid; Najafi, Rezvan; Mahdavinezhad, Ali; Ezati, Razie; Sotanian, Alireza; Amini, Razieh.
Afiliación
  • Hosseini N; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Khoshnazar A; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Saidijam M; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Azizi Jalilian F; b Microbiology Department, Faculty of Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Najafi R; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Mahdavinezhad A; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Ezati R; c Institute of Medical Biotechnology , National Institute of Genetic Engineering and Biotechnology , Tehran , Iran.
  • Sotanian A; d Modeling of Noncommunicable Disease Research Center , School of Public Health, Hamadan University of Medical Sciences , Hamadan , Iran.
  • Amini R; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
Nutr Cancer ; 71(1): 159-171, 2019.
Article en En | MEDLINE | ID: mdl-30650987
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-ß inhibitor, ZER + NF-ß 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.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sesquiterpenos / Activador de Plasminógeno de Tipo Uroquinasa / Neoplasias Colorrectales / FN-kappa B / Proteína-Tirosina Quinasas de Adhesión Focal / Inhibidores de las Quinasa Fosfoinosítidos-3 Idioma: En Revista: Nutr Cancer Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sesquiterpenos / Activador de Plasminógeno de Tipo Uroquinasa / Neoplasias Colorrectales / FN-kappa B / Proteína-Tirosina Quinasas de Adhesión Focal / Inhibidores de las Quinasa Fosfoinosítidos-3 Idioma: En Revista: Nutr Cancer Año: 2019 Tipo del documento: Article