Circular RNA hsa_circ_0032463 Acts as the Tumor Promoter in Osteosarcoma by Regulating the MicroRNA 498/LEF1 Axis

Guanghua Qin1, Xuejian Wu1

  • 1Department of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

Insights

Circular RNA hsa_circ_0032463 (circ_0032463) promotes osteosarcoma (OS) progression by regulating the miR-498/LEF1 axis. Upregulated circ_0032463 enhances OS cell migration and proliferation while inhibiting apoptosis.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Osteosarcoma (OS) is a primary bone malignancy with limited treatment options.
  • MicroRNAs (miRNAs) roles in OS are studied, but circular RNA (circRNA) mechanisms remain underexplored.
  • Circular RNAs are emerging as key regulators in various cancers, including OS.

Purpose of the Study:

  • To investigate the role and mechanism of hsa_circ_0032463 (circ_0032463) in osteosarcoma (OS) progression.
  • To elucidate the regulatory pathway involving circ_0032463, miRNA 489 (miR-498), and LEF1 in OS.

Main Methods:

  • Reverse transcription-quantitative PCR (RT-qPCR) to detect circ_0032463 expression in OS tissues and cell lines.
  • RNA pulldown, RNA immunoprecipitation (RIP), and luciferase assays to confirm interactions between circ_0032463, miR-498, and LEF1.
  • Cell proliferation, migration, and apoptosis assays (CCK-8, BrdU, wound healing, FITC) to assess functional impacts.

Main Results:

  • Circ_0032463 expression was significantly upregulated in OS tissues and cell lines.
  • Circ_0032463 directly interacted with miR-498, leading to decreased miR-498 levels in OS cells.
  • The circ_0032463/miR-498 axis modulated LEF1 expression, promoting OS cell migration and proliferation while suppressing apoptosis.

Conclusions:

  • Circ_0032463 acts as an oncogenic circRNA in osteosarcoma.
  • The identified circ_0032463/miR-498/LEF1 axis provides a novel therapeutic target for OS treatment.
  • Understanding circRNA functions is crucial for advancing OS research and therapy.

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