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mTOR Signaling in Metabolism and Cancer
Shile Huang1,2
1Department of Biochemistry and Molecular Biology, Louisiana State University Health Sciences Center, 1501 Kings Highway, Shreveport, LA 71130-3932, USA.
Abstract:
The mechanistic/mammalian target of rapamycin (mTOR), a serine/threonine kinase, is a central regulator for human physiological activity. Deregulated mTOR signaling is implicated in a variety of disorders, such as cancer, obesity, diabetes, and neurodegenerative diseases. The papers published in this special issue summarize the current understanding of the mTOR pathway and its role in the regulation of tissue regeneration, regulatory T cell differentiation and function, and different types of cancer including hematologic malignancies, skin, prostate, breast, and head and neck cancer. The findings highlight that targeting the mTOR pathway is a promising strategy to fight against certain human diseases.
Insights
The mechanistic/mammalian target of rapamycin (mTOR) pathway regulates physiological functions and is implicated in diseases like cancer and diabetes. Targeting mTOR shows promise for treating various human disorders.
Area of Science:
- Biochemistry and Molecular Biology
- Cellular Signaling
- Physiology
Background:
- The mechanistic/mammalian target of rapamycin (mTOR) is a key kinase regulating cellular processes.
- Aberrant mTOR signaling is linked to numerous pathologies, including cancer, metabolic disorders, and neurodegeneration.
Discussion:
- This special issue reviews mTOR's role in tissue regeneration and immune function, specifically regulatory T cell differentiation.
- It covers mTOR's involvement in diverse cancers: hematologic, skin, prostate, breast, and head and neck.
Key Insights:
- mTOR pathway dysregulation contributes to a spectrum of human diseases.
- The reviewed research consolidates current knowledge on mTOR signaling.
Outlook:
- Targeting the mTOR pathway presents a viable therapeutic strategy for various human diseases.
- Further research into mTOR signaling could unlock new treatment avenues.
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