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Role of miR-96/EVI1/miR-449a Axis in the Nasopharyngeal Carcinoma Cell Migration and Tumor Sphere Formation.
Chan, Lai-Sheung; Lung, Hong-Lok; Ngan, Roger Kai-Cheong; Lee, Anne Wing-Mui; Tsao, Sai Wah; Lo, Kwok-Wai; Kahn, Michael; Lung, Maria Li; Wieser, Rotraud; Mak, Nai-Ki.
Afiliação
  • Chan LS; Department of Biology, Hong Kong Baptist University, Kowloon Tong, Hong Kong, China.
  • Lung HL; Department of Chemistry, Hong Kong Baptist University, Kowloon Tong, Hong Kong, China.
  • Ngan RK; Department of Clinical Oncology, University of Hong Kong, Pokfulam, Hong Kong, China.
  • Lee AW; Center for Nasopharyngeal Carcinoma Research, University of Hong Kong, Pokfulam, Hong Kong, China.
  • Tsao SW; Department of Clinical Oncology, University of Hong Kong, Pokfulam, Hong Kong, China.
  • Lo KW; Center for Nasopharyngeal Carcinoma Research, University of Hong Kong, Pokfulam, Hong Kong, China.
  • Kahn M; Center for Nasopharyngeal Carcinoma Research, University of Hong Kong, Pokfulam, Hong Kong, China.
  • Lung ML; Department of Anatomy, University of Hong Kong, Pokfulam, Hong Kong, China.
  • Wieser R; Department of Anatomical and Cellular Pathology and State Key Laboratory in Oncology in South China, The Chinese University of Hong Kong, Central Ave, Hong Kong, China.
  • Mak NK; Department of Molecular Medicine, Beckman Research Institute at City of Hope, Duarte, CA 91010-3000, USA.
Int J Mol Sci ; 21(15)2020 Jul 31.
Article em En | MEDLINE | ID: mdl-32752071
ABSTRACT
The Wnt signaling pathway is one of the major signaling pathways used by cancer stem cells (CSC). Ecotropic Viral Integration Site 1 (EVI1) has recently been shown to regulate oncogenic development of tumor cells by interacting with multiple signaling pathways, including the Wnt signaling. In the present study, we found that the Wnt modulator ICG-001 could inhibit the expression of EVI1 in nasopharyngeal carcinoma (NPC) cells. Results from loss-of-function and gain-of-function studies revealed that EVI1 expression positively regulated both NPC cell migration and growth of CSC-enriched tumor spheres. Subsequent studies indicated ICG-001 inhibited EVI1 expression via upregulated expression of miR-96. Results from EVI1 3'UTR luciferase reporter assay confirmed that EVI1 is a direct target of miR-96. Further mechanistic studies revealed that ICG-001, overexpression of miR-96, or knockdown of EVI1 expression could restore the expression of miR-449a. The suppressive effect of miR-449a on the cell migration and tumor sphere formation was confirmed in NPC cells. Taken together, the miR-96/EVI1/miR-449a axis is a novel pathway involved in ICG-001-mediated inhibition of NPC cell migration and growth of the tumor spheres.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / Proteína do Locus do Complexo MDS1 e EVI1 / Carcinoma Nasofaríngeo Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / Proteína do Locus do Complexo MDS1 e EVI1 / Carcinoma Nasofaríngeo Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China