Cargando…

Curcumin Analog CH-5 Suppresses the Proliferation, Migration, and Invasion of the Human Gastric Cancer Cell Line HGC-27

Gastric cancer is one of the most frequent malignant tumors in the world. The majority of patients are diagnosed with metastatic gastric cancer, which has a low survival rate. These data reinforce the importance of studying the anticancer activity of new molecules with the potential to suppress gast...

Descripción completa

Detalles Bibliográficos
Autores principales: Silva, Gabriel, Teixeira Lima, Felipe, Seba, Viviane, Mendes Lourenço, Ana Laura, Lucas, Thaise Graminha, de Andrade, Bianca Vieira, Torrezan, Guilherme Silva, Polaquini, Carlos Roberto, Garcia, Marcelo Engracia, Couto, Lucélio Bernardes, Bestetti, Reinaldo Bulgarelli, de Castro França, Suzelei, Fachin, Ana Lúcia, Regasini, Luis Octavio, Marins, Mozart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017500/
https://www.ncbi.nlm.nih.gov/pubmed/29385675
http://dx.doi.org/10.3390/molecules23020279
Descripción
Sumario:Gastric cancer is one of the most frequent malignant tumors in the world. The majority of patients are diagnosed with metastatic gastric cancer, which has a low survival rate. These data reinforce the importance of studying the anticancer activity of new molecules with the potential to suppress gastric cancer metastasis. Curcumin is a well-studied compound that has demonstrated anti-metastatic effects. Here we investigated if CH-5, a curcumin derivative compound, has anti-metastatic properties in the human gastric cancer cell line HGC-27. Firstly, we found that CH-5 decreased viability and induced apoptosis in HGC-27 cells in a dose-dependent manner. Additionally, CH-5 suppressed the migration and invasion of HGC-27 cells by downregulating the expression and collagenase activity of matrix metalloproteinase 2 in a dose-dependent manner. In conclusion, CH-5 showed anticancer activities, including the induction of apoptosis, and the suppression of migration and invasion in HGC-27 cells, suggesting that CH-5 can be a lead molecule for the development of anti-metastatic drugs for gastric cancer therapy.