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Updated: Oct 24, 2025

In Silico Identification and Characterization of circRNAs During Host-Pathogen Interactions
Published on: October 21, 2022
CircMTO1: A circular RNA with roles in the carcinogenesis
Soudeh Ghafouri-Fard1, Tayybeh Khoshbakht2, Arefe Bahranian3
1Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:
Circular RNAs (circRNAs) have a closed loop structure which endows them high stability. These transcripts are made through back splicing instead of classical splicing and are abundant in the human transcriptome. Recent advances in the development and implementation of high-throughput sequencing methods in cooperation with novel bioinformatics tools have shown contribution of circRNAs in the developmental processes, physiological settings and pathoetiology of cancers. CircMTO1 is a circRNA which was firstly identified as a down-regulated circRNA in hepatocellular carcinoma through circRNA profiling using microarray technique. Subsequent independent studies in lung adenocarcinoma, colorectal cancer, bladder cancer, glioblastoma, prostate cancer, osteosarcoma, gastric cancer and ovarian cancer have verified down-regulation of circMTO1 in neoplastic tissues compared with non-neoplastic ones. However, expression of circMTO1 has been found to be up-regulated in cervical and gallbladder cancers. miR-17, miR-9, miR-221, miR-6893, miR-92, miR-219a-5p, miR-337, miR-630, miR-3200-5p and miR-199a-3p have been shown to be sequestered by circMTO1. This circRNA can regulate activity of Notch, Wnt/β-Catenin, TGF-β/Smad, JAK1/STAT3 and AMPK signaling pathways. In the current study, we review the literature on the role of circMTO1 in the tumorigenesis.
Insights
Circular RNAs (circRNAs) are stable molecules involved in cancer. CircMTO1, a specific circRNA, is often down-regulated in many cancers but up-regulated in others, impacting tumorigenesis.
Area of Science:
- Molecular Biology
- Genomics
- Cancer Research
Background:
- Circular RNAs (circRNAs) are unique RNA transcripts with a closed-loop structure, conferring high stability.
- Advances in sequencing and bioinformatics reveal circRNAs' roles in development, physiology, and cancer pathology.
- CircMTO1 was initially identified as downregulated in hepatocellular carcinoma and subsequently in various other cancers.
Purpose of the Study:
- To review the existing literature on the role of circMTO1 in tumorigenesis.
- To consolidate findings on circMTO1 expression patterns across different cancer types.
- To explore the molecular mechanisms by which circMTO1 influences cancer development.
Main Methods:
- Literature review of studies investigating circMTO1 expression and function in cancer.
- Analysis of circRNA profiling data, including microarray and sequencing techniques.
- Examination of experimental evidence linking circMTO1 to specific signaling pathways and microRNA interactions.
Main Results:
- CircMTO1 is predominantly downregulated in hepatocellular carcinoma, lung adenocarcinoma, colorectal cancer, bladder cancer, glioblastoma, prostate cancer, osteosarcoma, gastric cancer, and ovarian cancer.
- Conversely, circMTO1 expression is upregulated in cervical and gallbladder cancers.
- CircMTO1 sequesters various microRNAs (e.g., miR-17, miR-9, miR-221) and modulates key signaling pathways including Notch, Wnt/β-Catenin, TGF-β/Smad, JAK1/STAT3, and AMPK.
Conclusions:
- CircMTO1 exhibits diverse expression patterns in human cancers, suggesting context-dependent roles in tumorigenesis.
- Its ability to sponge microRNAs and regulate signaling pathways highlights its significance as a potential cancer biomarker and therapeutic target.
- Further research is warranted to fully elucidate the complex functions of circMTO1 in different oncological settings.
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