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The Colon-26 Carcinoma Tumor-bearing Mouse as a Model for the Study of Cancer Cachexia
Published on: November 30, 2016
MicroRNAs as potential therapeutic targets for muscle wasting during cancer cachexia
Anthony J Sannicandro1, Brian McDonagh1, Katarzyna Goljanek-Whysall1,2
1Discipline of Physiology, School of Medicine, National University of Ireland, Galway, Ireland.
Purpose Of Review:
Muscle wasting in cancer cachexia remains an unmet clinical need due to lack of effective therapies associated with the complexity of the disease. Here, we discuss microRNAs, robust regulators of the expression of multiple genes, only recently characterized in cancer cachexia in humans and their therapeutic potential for muscle wasting.
Recent Findings:
Changes in microRNAs in muscle of cancer patients have been demonstrated for the first time and these are associated with dysregulated signalling networks during muscle wasting. These data, together with studies in animal models, indicate that microRNAs are attractive therapeutic candidates for maintaining muscle mass, both during and following cancer treatment ultimately improving patient outcomes.
Summary:
Cancer cachexia is a complex metabolic condition associated with muscle wasting. Maintenance of muscle mass in cancer patients can improve their response to therapy and prognosis. microRNAs, which can act as oncogenes or tumour suppressors, are also dysregulated in muscle of cachexia patients. Studies in animal models of muscle wasting have demonstrated that microRNAs regulate muscle mass and strength. With more microRNA-based therapeutics in clinical trials and first RNA drugs approved, microRNAs present an attractive novel therapeutic avenue for maintaining muscle homeostasis in cachexia patients to improve their prognosis.
Insights
MicroRNAs, regulators of gene expression, are newly identified in human cancer cachexia muscle wasting. These molecules show therapeutic potential for preserving muscle mass and improving patient outcomes.
Area of Science:
- Biomedical Science
- Molecular Biology
- Oncology
Background:
- Cancer cachexia is a complex metabolic condition characterized by significant muscle wasting.
- Maintaining muscle mass is crucial for improving cancer patients' response to therapy and overall prognosis.
- Effective therapies for muscle wasting in cancer cachexia are currently limited, representing an unmet clinical need.
Purpose of the Study:
- To review the role of microRNAs in cancer cachexia and their therapeutic potential for muscle wasting.
- To highlight the recent characterization of microRNAs in human cancer cachexia.
- To discuss microRNAs as potential therapeutic targets for maintaining muscle homeostasis.
Main Methods:
- Review of current literature on microRNAs, cancer cachexia, and muscle wasting.
- Analysis of studies demonstrating microRNA changes in muscle of cancer patients.
- Examination of data from animal models investigating microRNA function in muscle wasting.
Main Results:
- MicroRNAs have been identified and characterized in the muscle tissue of cancer cachexia patients for the first time.
- Changes in microRNAs are associated with dysregulated signaling networks contributing to muscle wasting.
- Studies in animal models confirm that microRNAs regulate muscle mass and strength.
Conclusions:
- MicroRNAs are promising therapeutic candidates for combating muscle wasting in cancer cachexia.
- Targeting microRNAs offers a novel strategy to maintain muscle mass during and after cancer treatment.
- The development of microRNA-based therapeutics could significantly improve patient prognosis and outcomes in cancer cachexia.
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