The Role of Skeletal Muscle Intrinsic Clock on the Development and Progression of Cancer Cachexia

Author

Jason Lin

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.

Comments

Data is provided by the student.

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