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.

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.

Related Concept Videos

MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
3.3K
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After...
22.5K
Experimental RNAi02:15

Experimental RNAi

RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
6.6K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
4.0K
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
5.6K
piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
7.1K