Abstract
Abstract Purpose Esophageal squamous cell carcinoma (ESCC) is a highly aggressive gastrointestinal malignancy. This study aims to investigate the role and molecular mechanism of a novel circular RNA, circ_0001741, in ESCC progression. Methods The circular structure of circ_0001741 was confirmed by RNase R and actinomycin D assays alongside divergent primer-based amplification targeting its backsplice junction (BSJ). Its expression was profiled using an ESCC tissue microarray. Functional effects of circ_0001741 on proliferation and invasion were assessed using CCK-8 and Transwell assays. The interactions within the circ_0001741/miR-194-5p/E2F3 axis were validated through dual-luciferase reporter, RNA pull-down, and rescue experiments. Results Circ_0001741 was significantly upregulated in ESCC tissues with a 7.5-fold increase compared to adjacent normal tissues. Functional assays demonstrated that silencing circ_0001741 markedly inhibited ESCC cell proliferation and invasion significantly. Mechanistically, circ_0001741 directly sponged miR-194-5p, leading to the upregulation of its target oncogene E2F3. Crucially, the anti-tumor effects induced by circ_0001741 knockdown were significantly reversed by co-silencing miR-194-5p or overexpressing E2F3, thus establishing a functional circ_0001741/miR-194-5p/E2F3 axis in ESCC. Conclusion Our findings establish that circ_0001741 drives ESCC progression by modulating the miR-194-5p/E2F3 axis, underscoring its therapeutic potential for ESCC treatment.
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Publication Info
- Year
- 2025
- Type
- article
- Citations
- 0
- Access
- Closed
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- DOI
- 10.1186/s12957-025-04124-2
- PMID
- 41372977