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FOXD2-AS1 acts an oncogene in esophageal squamous cell carcinoma through sponging miR-204-3p

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Abstract

Purpose

A growing number of evidences has revealed that long non-coding RNAs (lncRNAs) have vital effect in the pathogenesis of esophageal squamous cell carcinoma (ESCC). In our work, we found that lncRNA FOXD2 adjacent opposite strand RNA 1 (FOXD2-AS1) was significantly increased in clinical ESCC samples and cell lines.

Methods

The biological effect of FOXD2-AS1 on EC109 and KYSE150 cells showed that the low expression of FOXD2-AS1 inhibited the proliferation through CCK8 and colony formation assays, invasion by transwell chamber test, migration abilities by wound healing assay, and enhance apoptosis rates by flow cytometry assay.

Results

Through bioinformatics analysis and luciferase reporter assays, microRNA (miR)-204-3p was proved to be a target of FOXD2-AS1. We further confirmed that FOXD2-AS1 was the upstream inhibitor of miR-204-3p and the down-regulation of miR-204-3p reversed the repressive effects of low expression of FOXD2-AS1 on ESCC progression. In addition, inhibition of FOXD2-AS1 effectively suppressed the tumor growth.

Conclusions

In general, our results suggested that FOXD2-AS1 may be of vital therapeutic importance for the treatment of ESCC patients.

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Funding

This work was supported by State Key Laboratory of Pathogenesis, Prevention and Treatment of Central Asian High Incidence Diseases Fund (SKL-HIDCA-2020-13).

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Authors and Affiliations

Authors

Contributions

DL conceived and designed the study, and drafted the manuscript. AS and HL collected, analyzed and interpreted the experimental data. YW and YG revised the manuscript for important intellectual content. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Dongbo Luo.

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Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

All procedures involving human participants were performed in accordance with the ethical standards of the Institutional and National Research Committee, and with the Declaration of Helsinki. Ethical approval was obtained from the Ethical Committee of the Affiliated Tumor Hospital of Xinjiang Medical University.

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Supplementary Information

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12094_2022_2850_MOESM1_ESM.pdf

Fig. S1 The correlation between progression-free survival and FOXD2-AS1 expression was detected by bioinformatic analysis (PDF 40 kb)

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Luo, D., Salai, A., Lv, H. et al. FOXD2-AS1 acts an oncogene in esophageal squamous cell carcinoma through sponging miR-204-3p. Clin Transl Oncol 24, 1954–1963 (2022). https://doi.org/10.1007/s12094-022-02850-7

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  • DOI: https://doi.org/10.1007/s12094-022-02850-7

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