Role of CircRNAs_100395 in Proliferation and Metastases of Liver Cancer.

Med Sci Monit

Department of Vascular Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China (mainland).

Published: August 2019

AI Article Synopsis

  • Circular RNAs, particularly circRNA_100395, are noncoding RNAs involved in cancer regulation, showing downregulation in lung cancer and now identified as significant in liver cancer.
  • Evidence indicates that circ_100395 is also downregulated in liver cancer tissues, correlating with worse tumor characteristics but better postoperative survival rates for patients with higher levels.
  • Experiments demonstrate that increasing circ_100395 levels in liver cancer cells hampers their growth and invasion abilities, but this effect is counteracted by the microRNA miR-1228, suggesting circ_100395’s potential as a therapeutic target.

Article Abstract

BACKGROUND Circular RNAs (circRNAs) are a kind of noncoding RNA with high cancer-specific expression, and great potential in regulating tumorigenesis. Among these, circRNA_100395 (circ_100395) has been reported to be downregulated in lung cancer, and participates in the process of tumor cell proliferation and metastasis. However, its expression and function in liver cancer remain unknown. MATERIAL AND METHODS Quantitative real-time polymerase chain reaction (RT-qPCR) was used to evaluate the expression level of circ_100395 and microRNAs-1228 (miR-1228) in liver cancer samples and the adjacent non-tumor tissues. Cell proliferation, apoptosis, invasion, migration, and epithelial-mesenchymal transition (EMT) pathway of circ_100395 upregulated cells were analyzed using a Cell Counting Kit-8 (CCK-8), flow cytometry, Transwell assay, and Western blot analysis. RESULTS We found that circ_100395 was downregulated in cancerous liver tissues relative to the adjacent normal tissues. The overexpression of circ_100395 was negatively associated with tumor differentiation, microvascular invasion, and portal vein tumor thrombosis. However, patients with higher circ_10039 expression tended to have better postoperative disease-free survival time. Moreover, upregulation of circ_100395 in liver cancer cells inhibited cell proliferation, induced apoptosis, then silenced the EMT pathway and reduced migration and invasion abilities, while this anti-tumor effect was significantly reversed by the downstream target, miR-1228. CONCLUSIONS circ_100395 appears to be a promising therapeutic target for liver cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709643PMC
http://dx.doi.org/10.12659/MSM.915963DOI Listing

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