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miR-107 promotes hepatocellular carcinoma cell proliferation by targeting Axin2.
Zhang, Jun-Jie; Wang, Chen-Yu; Hua, Long; Yao, Kun-Hou; Chen, Jiang-Tao; Hu, Jun-Hong.
Afiliação
  • Zhang JJ; Department of General Surgery, Huaihe Hospital of Henan University Kaifeng, 475000, Henan Province, China.
  • Wang CY; Department of General Surgery, Huaihe Hospital of Henan University Kaifeng, 475000, Henan Province, China.
  • Hua L; Department of General Surgery, Huaihe Hospital of Henan University Kaifeng, 475000, Henan Province, China.
  • Yao KH; Department of General Surgery, Huaihe Hospital of Henan University Kaifeng, 475000, Henan Province, China.
  • Chen JT; Department of General Surgery, Huaihe Hospital of Henan University Kaifeng, 475000, Henan Province, China.
  • Hu JH; Department of General Surgery, Huaihe Hospital of Henan University Kaifeng, 475000, Henan Province, China.
Int J Clin Exp Pathol ; 8(5): 5168-74, 2015.
Article em En | MEDLINE | ID: mdl-26191213
BACKGROUND: A large number of studies demonstrated that microRNAs play important roles in the progression and development of human cancers. However, the expression level of miR-107 and its biological function in hepatocellular carcinoma (HCC) remains unclear. METHOD: Quantitative real-time PCR (qRT-PCR) was used to evaluate the expression level of miR-107 in HCC tissues and cell lines. Then, we explored the function of miR-107 to determine its potential roles on HCC cell proliferation in vitro. Luciferase reporter assay was used to confirm the target gene of miR-107, and the results were validated in cell lines. RESULTS: miR-107 was significantly up-regulated in HCC tissues and cell lines. The enforced expression of miR-107 was able to promote cell proliferation in HepG2 cells. At the molecular level, our results suggested that expression of Axin2 was negatively regulated by miR-107. CONCLUSION: Our observations suggested that miR-107 could promote HCC cells proliferation via targeting Axin2 and might represent a potential therapeutic target for HCC.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / MicroRNAs / Proliferação de Células / Proteína Axina / Neoplasias Hepáticas Limite: Humans Idioma: En Revista: Int J Clin Exp Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / MicroRNAs / Proliferação de Células / Proteína Axina / Neoplasias Hepáticas Limite: Humans Idioma: En Revista: Int J Clin Exp Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China