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Related Experiment Video

Updated: May 14, 2026

Assessing Functional Metrics of Skeletal Muscle Health in Human Skeletal Muscle Microtissues
09:30

Assessing Functional Metrics of Skeletal Muscle Health in Human Skeletal Muscle Microtissues

Published on: February 18, 2021

MyoRep: A Novel Reporter System to Detect Early Muscle Atrophy In Vitro and In Vivo.

Andrea D Re Cecconi1, Nicoletta Rizzi2, Mara Barone1

  • 1Department of Neuroscience, Mario Negri Institute for Pharmacological Research IRCCS, Milan, Italy.

Journal of Cachexia, Sarcopenia and Muscle
|May 12, 2026
PubMed
Summary

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This summary is machine-generated.

This study developed a novel reporter system, MyoRep, to detect pathological muscle atrophy early. MyoRep distinguishes disease-related muscle wasting from physiological changes, enabling timely interventions for better patient outcomes.

Area of Science:

  • Biomedical Engineering
  • Molecular Biology
  • Genetics

Background:

  • Muscle atrophy is a significant predictor of mortality, occurring in both physiological (fasting) and pathological (cancer) conditions.
  • Distinguishing pathological from physiological muscle wasting is crucial for early therapeutic intervention.
  • Current methods lack the specificity to differentiate between types of muscle atrophy, hindering early detection.

Purpose of the Study:

  • To engineer a reporter system capable of tracking pathological muscle atrophy in vivo.
  • To differentiate pathological muscle wasting from physiological changes like fasting-induced atrophy.
  • To develop a tool for early prediction and monitoring of muscle wasting diseases.

Main Methods:

  • Compared upstream non-coding regions of atrophy-related genes (atrogenes) using the MuRF1 promoter.
Keywords:
cancer cachexiain vivo imagingmuscle atrophyreporter mouse

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Last Updated: May 14, 2026

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Published on: February 18, 2021

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  • Cloned selected promoters upstream of Firefly Luciferase for in vitro and in vivo validation.
  • Generated the MyoRep reporter mouse using the GREDEL promoter and AAV9 delivery systems for in vivo imaging.
  • Main Results:

    • The GREDEL promoter accurately detected early pathological muscle atrophy induced by sarcoma and denervation, preceding observable wasting by up to 8 days.
    • The TWIST promoter showed undesirable activity during fasting and dexamethasone treatment, unlike GREDEL.
    • MyoRep mice accurately predicted tumor-induced cachexia and sex-specific muscle wasting in ApcMin/+ mice, and responded to anti-atrophic drug administration.

    Conclusions:

    • The MyoRep reporter system reliably detects pathological muscle atrophy, distinguishing it from physiological changes.
    • MyoRep serves as an unprecedented tool for early prediction of muscle wasting in various diseases.
    • This system holds potential for identifying novel atrophy biomarkers and accelerating the development of anti-atrophic therapies.