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A siRNA-based method for efficient silencing of PYROXD1 gene expression in the colon cancer cell line HCT116.
Shabani, Samira; Mahjoubi, Frouzandeh; Moosavi, Mohammad A.
Afiliação
  • Shabani S; Department of Clinical Genetic, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran.
  • Mahjoubi F; Colorectal Research Centre (CRRC), Hazrate-Rasoule-Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Moosavi MA; Department of Clinical Genetic, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran.
J Cell Biochem ; 120(12): 19310-19317, 2019 12.
Article em En | MEDLINE | ID: mdl-31502705
PURPOSE: The aim of this study was to determine the biological function of pyridine nucleotide-disulfide oxidoreductase domain 1 (PYROXD1), a recently discovered protein, in colon cancer cell line HCT116. METHODS: The small interfering RNA (siRNA) was designed rationally on the basis of the target sequence against PYROXD1. Relative PYROXD1 mRNA levels were measured by a quantitative real-time polymerase chain reaction. Flow cytometry was performed to monitor tumor cells proliferation and apoptosis after siRNA transfection. RESULTS: Knockdown of PYROXD1 arrested the cell cycle, and induced late apoptosis in colon cancer cell line HCT116 DISCUSSION: Taken together, these results revealed the critical roles of PYROXD1 in regulating cell cycle and apoptosis and possibly will signify its therapeutic potential for targeting colorectal cancer models.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / RNA Interferente Pequeno / Oxirredutases atuantes sobre Doadores de Grupo Enxofre Limite: Humans Idioma: En Revista: J Cell Biochem Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Irã País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / RNA Interferente Pequeno / Oxirredutases atuantes sobre Doadores de Grupo Enxofre Limite: Humans Idioma: En Revista: J Cell Biochem Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Irã País de publicação: Estados Unidos