CCCTC-binding factor regulates splicing factor proline and glutamine-rich to promote malignant growth of osteosarcoma

  • 0Spine Surgery, Affiliated Hospital of Jiangsu University Zhenjiang 212001, Jiangsu, China.

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Summary

This summary is machine-generated.

CCCTC-binding factor (CTCF) acts as an oncogene in osteosarcoma by increasing splicing factor proline and glutamine-rich (SFPQ) expression. Targeting the CTCF-SFPQ pathway may offer new osteosarcoma treatment strategies.

Area Of Science

  • Oncology
  • Molecular Biology
  • Gene Regulation

Background

  • CCCTC-binding factor (CTCF) is implicated in various cancers, but its role in osteosarcoma is unclear.
  • Splicing factor proline and glutamine-rich (SFPQ) is recognized as an oncogene in osteosarcoma.
  • Bioinformatic analysis suggests CTCF may regulate SFPQ transcription.

Purpose Of The Study

  • To investigate the function and mechanism of CTCF in osteosarcoma.
  • To explore the regulatory relationship between CTCF and SFPQ in osteosarcoma.

Main Methods

  • Bioinformatic analysis identified potential transcription factors for SFPQ.
  • Quantitative real-time PCR (qRT-PCR) and western blotting (WB) assessed CTCF expression.
  • Cell function assays, dual-luciferase reporter assays, and rescue experiments evaluated CTCF and SFPQ effects.

Main Results

  • CTCF and SFPQ showed a moderate correlation; CTCF was significantly expressed in osteosarcoma.
  • CTCF overexpression boosted osteosarcoma cell proliferation, migration, and invasion.
  • CTCF directly upregulated SFPQ by binding to its promoter; SFPQ knockdown counteracted CTCF's oncogenic effects.

Conclusions

  • CTCF promotes osteosarcoma malignancy by upregulating SFPQ, functioning as an oncogene.
  • The CTCF-SFPQ axis presents a potential therapeutic target for osteosarcoma treatment.

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