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The crucial role of miR-126 on suppressing progression of esophageal cancer by targeting VEGF-A.
Kong, Ranran; Ma, Yuefeng; Feng, Jie; Li, Shaomin; Zhang, Wei; Jiang, Jiantao; Zhang, Jin; Qiao, Zhe; Yang, Xiaoping; Zhou, Bin.
Afiliación
  • Kong R; Department of Thoracic Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, 710004 Xi'an, Shaanxi China.
  • Ma Y; Department of Thoracic Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, 710004 Xi'an, Shaanxi China.
  • Feng J; Department of Nephrology, The First Affiliated Hospital, Xi'an Jiaotong University, 710061 Xi'an, Shaanxi China.
  • Li S; Department of Thoracic Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, 710004 Xi'an, Shaanxi China.
  • Zhang W; Department of Thoracic Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, 710004 Xi'an, Shaanxi China.
  • Jiang J; Department of Thoracic Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, 710004 Xi'an, Shaanxi China.
  • Zhang J; Department of Thoracic Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, 710004 Xi'an, Shaanxi China.
  • Qiao Z; Department of Thoracic Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, 710004 Xi'an, Shaanxi China.
  • Yang X; Department of Thoracic Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, 710004 Xi'an, Shaanxi China.
  • Zhou B; Department of Thoracic Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, 710004 Xi'an, Shaanxi China.
Cell Mol Biol Lett ; 21: 3, 2016.
Article en En | MEDLINE | ID: mdl-28536606
ABSTRACT

BACKGROUND:

miR-126 is a key regulator of oncogenic processes. It is functionally linked to cellular proliferation, survival and migration. Vascular endothelial growth factor A (VEGF-A), which is regarded as a tumorgenesis activator, could directly target miR-126 in several tumors. However, the mechanism in esophageal cancer remains unclear. METHODS AND

RESULTS:

In this study, the expression of miR-126 and VEGF-A were assessed in esophageal cancer tissues and esophageal cancer cell lines. We found that miR-126 has significantly lower expression in esophageal cancer tissues and esophageal cancer cell lines than in healthy tissues, while the expression of VEGF-A is high. Luciferase reporter assays were performed to investigate the relationship between VEGF-A and miR-126. We confirmed that VEGF-A is a target for miR-126. Furthermore, the proliferation of esophageal cancer cells with miR-126 overexpression and miR-126 knockdown was monitored using the MTT assay. The results showed that miR-126 could inhibit esophageal cancer cell proliferation in vitro. The effect of miR-126 was also detected in BALB/c nude mice with transplanted esophageal cancer cells. In vivo study showed that tumor growth was significantly suppressed by miR-126 overexpression.

CONCLUSIONS:

We believe that restoring miR-126 levels may be a promising therapeutic approach in cases of esophageal cancer.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Esofágicas / Genes Supresores de Tumor / MicroARNs / Factor A de Crecimiento Endotelial Vascular Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Cell Mol Biol Lett Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Esofágicas / Genes Supresores de Tumor / MicroARNs / Factor A de Crecimiento Endotelial Vascular Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Cell Mol Biol Lett Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article