Crosstalk between the mTOR pathway and primary cilia in human diseases.
Autophagy is a fundamental catabolic process whereby excessive or damaged cytoplasmic components are degraded through lysosomes to maintain cellular homeostasis. Studies of mTOR signaling have revealed that mTOR controls biomass generation and metabolism by modulating key cellular processes, including protein synthesis and autophagy. Primary cilia, the assembly of which depends on kinesin molecular motors, serve as sensory organelles and signaling platforms. Given these pathways' central role in maintaining cellular and physiological homeostasis, a connection between mTOR and primary cilia signaling is starting to emerge in a variety of diseases. In this review, we highlight recent advances in our understanding of the complex crosstalk between the mTOR pathway and cilia and discuss its function in the context of related diseases.
Duke Scholars
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Related Subject Headings
- TOR Serine-Threonine Kinases
- Signal Transduction
- Humans
- Homeostasis
- Developmental Biology
- Cilia
- Autophagy
- 3102 Bioinformatics and computational biology
- 1114 Paediatrics and Reproductive Medicine
- 0601 Biochemistry and Cell Biology
Citation
DOI
Publication Date
Volume
Start / End Page
Related Subject Headings
- TOR Serine-Threonine Kinases
- Signal Transduction
- Humans
- Homeostasis
- Developmental Biology
- Cilia
- Autophagy
- 3102 Bioinformatics and computational biology
- 1114 Paediatrics and Reproductive Medicine
- 0601 Biochemistry and Cell Biology