Study on the Role of Circular RNA hsa_circ_0001591 in Colorectal Cancer

Authors

    Guoqing Feng, Zhanfei She, Haoyu Xu, Meina Cao, Zhipeng Liu Baotou Medical College, Inner Mongolia University of Science and Technology, Baotou 014010, Inner Mongolia, China Ordos Central Hospital, Inner Mongolia Autonomous Region, Ordos 017000, Inner Mongolia, China General Surgery Department, Ordos Central Hospital, Inner Mongolia Autonomous Region, Ordos 017000, Inner Mongolia, China Molecular Medicine Laboratory, Ordos Central Hospital, Inner Mongolia Autonomous Region, Ordos 017000, Inner Mongolia, China General Surgery Department, Ordos Central Hospital, Inner Mongolia Autonomous Region, Ordos 017000, Inner Mongolia, China

DOI:

https://doi.org/10.18063/apm.v10i2.877

Keywords:

Colorectal cancer, Whole transcriptome sequencing, Gene differential expression, Circular RNA, hsa_circ_0001591

Abstract

Objective: To validate and characterize the expression of circular RNA hsa_circ_0001591—identified by high-throughput sequencing on the DNBSEQ platform—as differentially expressed in colorectal cancer (CRC) tissues versus adjacent non-tumor tissues and to explore its association with clinicopathological features and prognostic potential. Methods: RT-qPCR was performed on 13 paired CRC and matched adjacent samples to confirm elevated hsa_circ_0001591 levels, functional knockdown attempts were made in CRC cell lines with PCR verification of silencing efficiency, and statistical analyses were conducted to correlate RNA expression with CD31/CD34 status, patient age, and short-term postoperative outcomes. Results: Ten of 13 CRC specimens showed significantly higher hsa_circ_0001591 expression in tumor versus adjacent tissue, and elevated levels correlated with CD31/CD34 positivity (P = 0.041) and age > 70 years old (P = 0.033), whereas circRNA knockdown in vitro was inconclusive due to its inherent stability and no significant differences in short-term postoperative status were observed. Conclusion: hsa_circ_0001591 is upregulated in CRC and linked to markers of vascular invasion, suggesting a potential inhibitory role in angiogenesis, and its miRNA/mRNA interaction network may drive CRC pathogenesis, making it a promising molecular biomarker and therapeutic target.

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Published

2025-06-28