A novel feedback regulated loop of circRRM2-IGF2BP1-MYC promotes breast cancer metastasis

Ran Hao; Lei Zhang; Yangming Si; Peng Zhang; Yipeng Wang; Bangchao Li; Jie Hu; Yixin Qi

doi:10.1186/s12935-023-02895-w

A novel feedback regulated loop of circRRM2-IGF2BP1-MYC promotes breast cancer metastasis

Cancer Cell Int. 2023 Mar 25;23(1):54. doi: 10.1186/s12935-023-02895-w.

Authors

Ran Hao^#¹, Lei Zhang^#¹, Yangming Si^#², Peng Zhang^{1

3}, Yipeng Wang¹, Bangchao Li⁴, Jie Hu⁵, Yixin Qi⁶

Affiliations

¹ Institutes of Health Research, Hebei Medical University, Shijiazhuang, Hebei, China.
² School of Physical Science and Technology, Inner Mongolia University, Hohhot, Inner Mongolia, China.
³ Department of Military Nursing, NCO School, Army Medical University, Shijiazhuang, Hebei, China.
⁴ Department of Breast Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
⁵ Department of Science and Technology, Hebei Medical University, Shijiazhuang, Hebei, China. Hujie@hebmu.edu.cn.
⁶ Department of Breast Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China. qiyixin@hebmu.edu.cn.

^# Contributed equally.

Abstract

Background: Metastasis is the leading cause of mortality in patients with breast cancer (BC). Studies demonstrate that circular RNAs (circRNAs) were involved in BC progression, while the molecular mechanisms remain largely unclear.

Methods: The microArray circRNA profiles were used to explore the differential expression circRNAs in BC and paracancerous normal tissues, and the quantitative reverse transcription-polymerase chain reaction was used to validate their expression level in clinical samples and cell lines. Nuclear/cytosolic fractionation and fluorescence in situ hybridization (FISH) assays were performed to examine circRRM2 (hsa_circ_0052582) subcellular location. The scratch wound healing and transwell assays were conducted to evaluate the impact of circRRM2 on BC cell migration and invasion. We predicted miRNAs that might bind with cricRRM2 and the downstream target genes using bioinformatics analysis and explored their expression levels and prognostic value in BC. FISH, RNA immunoprecipitation, Co-immunoprecipitation, Western blot, and rescue experiments were implemented to figure out circRRM2 function and underlying mechanisms in BC.

Results: The present study revealed several aberrant circRNAs in BC tissues and observed that circRRM2 was upregulated in tumor tissues of 40 patients with BC. High circRRM2 was significantly associated with advanced N stage in patients with BC. Gain- and loss- of function experiments revealed that circRRM2 promoted the migration and invasion of cells and functioned as an oncogene in BC. Mechanism studies showed that circRRM2 competed with miR-31-5p/miR-27b-3p to upregulate the IGF2BP1 expression. Furthermore, IGF2BP1 upregulated the circRRM2 level via interacting with MYC, which functioned as the transcriptional factor of circRRM2. Thus, the positive feedback loop that was composed of circRRM2/IGF2BP1/MYC was identified.

Conclusion: This study confirms that upregulated circRRM2 functions an oncogenic role in BC metastasis. The positive feedback loop of circRRM2/IGF2BP1/MYC enforces the circRRM2 expression, which might offer a potential target for BC treatment.

Keywords: Breast cancer; Circular RNA; Feedback loop; MYC; Metastasis.

Abstract

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