MicroRNA-26a induces osteosarcoma cell growth and metastasis via the Wnt/β-catenin pathway

Feng Qu1, Chun-Bao Li2, Bang-Tuo Yuan2

  • 1Department of Orthopedics, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, P.R. China; Department of Orthopedics, Chinese People's Liberation Army General Hospital, Beijing 100853, P.R. China.

Oncology Letters
|February 20, 2016
PubMed

Insights

MicroRNAs (miRNAs) regulate gene expression. This study found miR-26a is upregulated in osteosarcoma (OS) and promotes OS cell proliferation, migration, and invasion by targeting GSK-3β.

Area of Science:

  • Molecular Biology
  • Genetics
  • Oncology

Background:

  • MicroRNAs (miRNAs) are crucial regulators of gene expression.
  • Aberrant miRNA expression is common in human osteosarcoma (OS).

Purpose of the Study:

  • To investigate the role of miR-26a in osteosarcoma progression and metastasis.
  • To elucidate the molecular mechanism underlying miR-26a's function in OS.

Main Methods:

  • Reverse transcription-quantitative polymerase chain reaction (RT-qPCR).
  • Luciferase activity assay, cell viability, migration, and invasion assays.
  • Western blot analysis and cell transfection.

Main Results:

  • miR-26a was significantly upregulated in OS tissues and cell lines.
  • Overexpression of miR-26a enhanced proliferation, migration, and invasion of OS Saos-2 cells.
  • miR-26a directly targets glycogen synthase kinase-3β (GSK-3β) by binding to its 3'-UTR, inhibiting GSK-3β expression.

Conclusions:

  • miR-26a plays a significant role in osteosarcoma proliferation.
  • miR-26a promotes OS progression by directly regulating the Wnt/β-catenin signaling pathway via GSK-3β inhibition.

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