Circ_0001741 exerts as a tumor promoter in ovarian cancer through the regulation of miR-491-5p/PRSS8 axis

  • 0Department of Gynaecology, Yi Chang Maternal and Child Health Hospital, 99 Chengdong Avenue, Wujiagang District, Yichang City, 443001, Hubei, China. wangding@163.com.

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Summary

This summary is machine-generated.

Circular RNA (circRNA) circ_0001741 promotes ovarian cancer (OC) growth and metastasis by interacting with miR-491-5p and PRSS8. This pathway offers a potential molecular target for OC treatment.

Area Of Science

  • Oncology
  • Molecular Biology
  • Genetics

Background

  • Circular RNAs (circRNAs) are key regulators in ovarian cancer (OC).
  • Circ_0001741 is highly expressed in OC and influences paclitaxel resistance.
  • Understanding circ_0001741's mechanism is crucial for OC progression.

Purpose Of The Study

  • To investigate the role of circ_0001741 in ovarian cancer.
  • To elucidate the molecular mechanism of circ_0001741 in OC progression.
  • To explore circ_0001741 as a potential therapeutic target for OC.

Main Methods

  • Quantification of circ_0001741, miR-491-5p, and PRSS8 levels using qRT-PCR and Western blot.
  • Assessment of OC cell proliferation, apoptosis, and metastasis via CCK-8, Edu, flow cytometry, and Transwell assays.
  • Validation of RNA interactions using dual-luciferase reporter and RIP assays; in vivo assessment via xenograft assay.

Main Results

  • Circ_0001741 expression is upregulated in OC tissues and cell lines.
  • Circ_0001741 knockdown inhibits OC cell proliferation, metastasis, and enhances apoptosis.
  • Circ_0001741 targets miR-491-5p, which in turn targets PRSS8, promoting OC progression.

Conclusions

  • Circ_0001741 promotes OC cell growth and metastasis via the miR-491-5p/PRSS8 axis.
  • This pathway represents a potential molecular target for ovarian cancer therapy.
  • Circ_0001741 knockdown inhibits tumor growth in vivo.

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