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Updated: Feb 11, 2026

Author Spotlight: Exploring the Role of FAM83A in Cervical Cancer
Published on: February 9, 2024
The expanding role of mTOR in cancer cell growth and proliferation
Marie Cargnello1, Joseph Tcherkezian2, Philippe P Roux3
1Institute for Research in Immunology and Cancer (IRIC), Université de Montréal, Montréal, Québec, Canada.
Abstract:
The mechanistic/mammalian target of rapamycin (mTOR) is a conserved protein kinase that controls several anabolic processes required for cell growth and proliferation. As such, mTOR has been implicated in an increasing number of pathological conditions, including cancer, obesity, type 2 diabetes and neurodegeneration. As part of the mTOR complex 1 (mTORC1), mTOR regulates cell growth by promoting the biosynthesis of proteins, lipids and nucleic acids. Several mTORC1 substrates have been shown to regulate protein synthesis, including the eukaryotic initiation factor 4E (eIF4E)-binding proteins (4E-BPs) and the ribosomal S6 kinases (S6Ks) 1 and 2. In this work, we focus on the signalling pathways that lie both upstream and downstream of mTORC1, as well as their relevance to human pathologies. We further discuss pharmacological approaches that target mTOR and their applications for the treatment of cancer.
Insights
The mechanistic/mammalian target of rapamycin (mTOR) pathway regulates cell growth and is implicated in diseases like cancer. This study explores mTOR signaling, its role in pathology, and targeted cancer therapies.
Area of Science:
- Biochemistry and molecular biology
- Cellular signaling pathways
- Disease mechanisms
Background:
- The mechanistic/mammalian target of rapamycin (mTOR) is a key protein kinase controlling cell growth and proliferation.
- mTOR signaling is dysregulated in various pathologies, including cancer, obesity, type 2 diabetes, and neurodegeneration.
- mTOR complex 1 (mTORC1) regulates anabolic processes, including protein, lipid, and nucleic acid biosynthesis, via substrates like 4E-BPs and S6Ks.
Purpose of the Study:
- To elucidate the signaling pathways upstream and downstream of mTORC1.
- To examine the relevance of these pathways in human diseases.
- To review pharmacological strategies targeting mTOR for cancer treatment.
Main Methods:
- Review of existing literature on mTOR signaling pathways.
- Analysis of mTORC1 substrates and their roles in cellular processes.
- Exploration of therapeutic interventions targeting the mTOR pathway.
Main Results:
- Detailed examination of upstream and downstream signaling networks of mTORC1.
- Established links between mTOR dysregulation and the pathogenesis of major human diseases.
- Identified pharmacological agents targeting mTOR with potential in cancer therapy.
Conclusions:
- The mTOR pathway is a critical regulator of cell growth with significant implications in human diseases.
- Understanding mTOR signaling is crucial for developing targeted therapies, particularly for cancer.
- Pharmacological targeting of mTOR offers promising therapeutic avenues for various pathological conditions.
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