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Gomisin G Suppresses the Growth of Colon Cancer Cells by Attenuation of AKT Phosphorylation and Arrest of Cell Cycle Progression
Biomolecules & Therapeutics ; : 210-215, 2019.
Artigo em Inglês | WPRIM | ID: wpr-739656
ABSTRACT
Colorectal cancer is one of the leading causes of cancer related death due to a poor prognosis. In this study, we investigated the effect of Gomisin G on colon cancer growth and examined the underlying mechanism of action. We found that Gomisin G significantly suppressed the viability and colony formation of LoVo cells. Gomisin G reduced the phosphorylation level of AKT implying that Gomisin G suppressed the PI3K-AKT signaling pathway. Gomisin G also induced apoptosis shown by Annexin V staining and an increased level of cleaved poly-ADP ribose polymerase (PARP) and Caspase-3 proteins. Furthermore, Gomisin G remarkably triggered the accumulation of cells at the sub-G1 phase which represents apoptotic cells. In addition, the level of cyclin D1 and phosphorylated retinoblastoma tumor suppressor protein (Rb) was also reduced by the treatment with Gomisin G thus curtailing cell cycle progression. These findings show the suppressive effect of Gomisin G by inhibiting proliferation and inducing apoptosis in LoVo cells. Taken together, these results suggest Gomisin G could be developed as a potential therapeutic compound against colon cancer.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fosforilação / Prognóstico / Retinoblastoma / Ribose / Neoplasias Colorretais / Ciclo Celular / Apoptose / Anexina A5 / Colo / Neoplasias do Colo Tipo de estudo: Estudo prognóstico Idioma: Inglês Revista: Biomolecules & Therapeutics Ano de publicação: 2019 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fosforilação / Prognóstico / Retinoblastoma / Ribose / Neoplasias Colorretais / Ciclo Celular / Apoptose / Anexina A5 / Colo / Neoplasias do Colo Tipo de estudo: Estudo prognóstico Idioma: Inglês Revista: Biomolecules & Therapeutics Ano de publicação: 2019 Tipo de documento: Artigo