Electronic Theses and Dissertations
Date
2022
Document Type
Thesis
Degree Name
Master of Science
Department
Health Studies
Committee Chair
Melissa Puppa
Committee Member
James JC Carson
Committee Member
Chida CR Ramanathan
Abstract
Cancer cachexia is a chronic wasting disorder characterized by severe loss of skeletal muscle that affects approximately 80% of cancer patients. Altered rest-activity is a hallmark of circadian disruption and is often seen in cachectic patients. It is unknown how skeletal muscle clock gene expression is altered with the progression of cachexia. We investigated skeletal muscle clock gene expression during cachexia. Tissue from ApcMin/+ mice (MIN) were harvested in the morning and evening and were analyzed for clock gene expression. Per 2 and Per 3 increased expression in the evening. Rev-ERBα showed decreased expression in BL – 6 mice in the evening. RORα showed increased expression in BL – 6 mice in the evening. BL – 6 evening was significantly higher than compared to MIN evening. In conclusion, circadian clock expression is altered in a cachectic environment. Understanding the role of the muscle-specific circadian clock could lead to therapeutic interventions to attenuate cachexia.
Library Comment
Dissertation or thesis originally submitted to ProQuest.
Notes
Open access
Recommended Citation
Lin, Jason, "The Role of Skeletal Muscle Intrinsic Clock on the Development and Progression of Cancer Cachexia" (2022). Electronic Theses and Dissertations. 3391.
https://digitalcommons.memphis.edu/etd/3391
Comments
Data is provided by the student.