# Circ_0020460 drives tumorigenesis in cervical cancer through miR-485-3p sponging

**Authors:** Kun Yan, Chunyan Hu, Yali Cheng, Lingzhi Zheng, Baojin Zeng, Sujun Zhao, Chen Liu

PMC · DOI: 10.1007/s12672-024-00933-1 · Discover. Oncology · 2024-03-27

## TL;DR

This study shows that a circular RNA called circ_0020460 promotes cervical cancer growth by acting as a sponge for miR-485-3p, which in turn affects CXCL1 expression.

## Contribution

The study identifies a novel regulatory axis involving circ_0020460, miR-485-3p, and CXCL1 in cervical cancer progression.

## Key findings

- Circ_0020460 knockdown reduces cervical cancer cell proliferation, migration, invasion, and angiogenesis while promoting apoptosis.
- Circ_0020460 functions as a miR-485-3p sponge, and miR-485-3p targets CXCL1 to suppress tumor growth.
- Circ_0020460 downregulation inhibits xenograft tumor growth in vivo.

## Abstract

Deregulation of circular RNAs (circRNAs) is widely recognized in cancer progression. Our study aims to investigate the role of circ_0020460 in the development of cervical cancer (CC) and its potential mechanism of action. Quantitative real-time polymerase chain reaction (qRT-PCR) and western blot assays were used to detect the expression levels of circ_0020460, miR-485-3p and C-X-C motif chemokine ligand 1 (CXCL1). The roles of circ_0020460 on cell proliferation, cell migration, cell invasion, cell apoptosis, and angiogenesis were investigated using cell counting kit-8 (CCK-8) and Ethynyl deoxyuridine (Edu) assay, wound healing assay, transwell assay, flow cytometry assay, and tube formation assay, respectively. The putative relationship predicted by bioinformatics analysis was verified by dual-luciferase reporter assay and RNA immunoprecipitation (RIP) assay. Xenograft models were constructed to explore the role of circ_0020460 in vivo. The expression of circ_0020460 and CXCL1 expression were increased, while miR-485-3p expression was declined in CC tissues and cells. Circ_0020460 knockdown suppressed CC cell proliferation, cell migration, cell invasion, angiogenesis, and promoted cell apoptosis. Circ_0020460 functioned as a miR-485-3p sponge to inhibit miR-485-3p level, and the anti-cancer effects mediated by circ_0020460 knockdown were reversed by miR-485-3p inhibitor. MiR-485-3p bound to CXCL1 3ʹ untranslated region (3ʹUTR) to degrade CXCL1 expression, and the anti-cancer effects of miR-485-3p restoration were impaired by CXCL1 overexpression. Circ_0020460 downregulation inhibited CC xenograft tumor growth. These results suggest that circ_0020460 promoted the malignant behavior of CC cells by modulating the miR-485-3p/CXCL1 axis.

The online version contains supplementary material available at 10.1007/s12672-024-00933-1.

## Linked entities

- **Genes:** CXCL1 (C-X-C motif chemokine ligand 1) [NCBI Gene 2919]
- **Proteins:** CXCL1 (C-X-C motif chemokine ligand 1)
- **Diseases:** cervical cancer (MONDO:0002974)

## Full-text entities

- **Genes:** CXCL1 (C-X-C motif chemokine ligand 1) [NCBI Gene 2919] {aka FSP, GRO1, GROa, MGSA, MGSA-a, NAP-3}
- **Diseases:** tumorigenesis (MESH:D063646), CC (MESH:D002583), cancer (MESH:D009369)
- **Chemicals:** Edu (-)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10973326/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC10973326/full.md

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Source: https://tomesphere.com/paper/PMC10973326