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Characterization of the Indirubin Derivative LDD970 as a Small Molecule Aurora Kinase A Inhibitor in Human Colorectal Cancer Cells
Immune Network ; : 110-115, 2017.
Artigo em Inglês | WPRIM | ID: wpr-51910
ABSTRACT
Aurora kinase A plays an essential role in mitosis including chromosome separation and cytokinesis. Aberrant expression and activity of Aurora kinase A is associated with numerous malignancies including colorectal cancer followed by poor prognosis. The aim of this study is to determine the inhibitory effects of LDD970, an indirubin derivative, on Aurora kinase A in HT29 colorectal cancer cells. In vitro kinase assay revealed that, LDD970 inhibited levels of activated Aurora kinase A (IC₅₀=0.37 mM). The inhibitory effects of LDD970 on Aurora kinase A, autophosphorylation and phosphorylation of histone H3 (Ser10), were confirmed by immunoblot analysis. Moreover, LDD970 inhibited migration of HT29 cells and upregulated apoptosis-related protein cleaved PARP. In cell viability assay, LDD970 was observed to suppress HT29 cell growth (GI₅₀=4.22 µM). Although further studies are required, results of the present study suggest that LDD970 provide a valuable insight into small molecule indirubin derivative for therapeutic potential in human colorectal cancer.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fosforilação / Fosfotransferases / Prognóstico / Técnicas In Vitro / Histonas / Neoplasias Colorretais / Sobrevivência Celular / Células HT29 / Citocinese / Aurora Quinase A Tipo de estudo: Estudo prognóstico Limite: Humanos Idioma: Inglês Revista: Immune Network Ano de publicação: 2017 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fosforilação / Fosfotransferases / Prognóstico / Técnicas In Vitro / Histonas / Neoplasias Colorretais / Sobrevivência Celular / Células HT29 / Citocinese / Aurora Quinase A Tipo de estudo: Estudo prognóstico Limite: Humanos Idioma: Inglês Revista: Immune Network Ano de publicação: 2017 Tipo de documento: Artigo