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Related Concept Videos

MicroRNAs01:22

MicroRNAs

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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...
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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...
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Microorganisms in Medicine and Therapeutics01:29

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Microorganisms play a fundamental role in vaccine development, gene therapy, and therapeutic production. Their biological properties are harnessed to advance medicine and public health. Beyond immunization, microorganisms contribute to gut health, antibiotic synthesis, and genetic disease treatment.Live Attenuated and Inactivated VaccinesLive attenuated vaccines, such as the measles, mumps, and rubella (MMR) vaccine, utilize weakened forms of pathogens to closely resemble natural infections.
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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.
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Related Experiment Video

Updated: Apr 15, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
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MicroRNAs and oncolytic viruses.

Autumn J Ruiz1, Stephen J Russell1

  • 1Department of Molecular Medicine, Mayo Clinic College of Medicine, Rochester, MN 55905, United States.

Current Opinion in Virology
|April 13, 2015
PubMed
Summary

MicroRNAs control gene expression and can be engineered into oncolytic viruses to target cancer. This strategy enhances therapeutic efficacy and safety for potent cancer treatment.

Area of Science:

  • Molecular Biology
  • Genetics
  • Virology

Background:

  • MicroRNAs (miRNAs) are key regulators of gene expression in mammals, often showing tissue-specific patterns.
  • Oncolytic viruses (OVs) are engineered to selectively infect and kill cancer cells.
  • Targeting strategies are crucial for enhancing the safety and efficacy of OV-based therapies.

Purpose of the Study:

  • To explore the use of miRNA target sequences for tissue-specific control of gene expression and viral tropism.
  • To investigate the combination of miRNA regulation with oncolytic virotherapy for improved cancer treatment.
  • To enhance the therapeutic index of oncolytic viruses and miRNA-based therapeutics.

Main Methods:

  • Incorporating miRNA target sequences into exogenous genes and viral genomes.

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  • Developing unattenuated oncolytic viruses with enhanced potency and broad tropisms.
  • Utilizing oncolytic viruses to deliver and enhance miRNA-based therapeutics (restorative or inhibitory).
  • Main Results:

    • Engineered oncolytic viruses demonstrated enhanced potency and reduced off-target toxicities in multiple tissues.
    • The strategy allowed for simultaneous control of gene expression and viral tropism in specific tissues.
    • Combination therapy showed increased delivery, duration, and therapeutic efficacy of miRNA-based treatments.

    Conclusions:

    • Combining oncolytic virotherapy with miRNA regulation represents a potent and safe approach for cancer therapeutics.
    • This strategy offers precise control over gene expression and viral targeting, improving therapeutic outcomes.
    • Further development holds promise for next-generation cancer treatments with enhanced specificity and reduced side effects.