The mTOR signalingpathway (mechanistic Target of Rapamycin mTOR) is a central regulator of cell growth, metabolism, and survival. It integrates signals from nutrients, growth factors, and cellular energy status to maintain homeostasis and adapt to environmental changes.
Why choose AnyGenes® for mTOR pathway research?
At AnyGenes®, we offer advanced qPCR arrays tailored for mTOR pathway research. With our innovative solutions, researchers can:
Investigate key regulators of the mTOR pathway, such as mTORC1, mTORC2, and AMPK.
Analyze downstream targets like S6K, 4E-BP1, and autophagy-related genes.
Study the crosstalk between mTOR and other pathways, including PI3K/AKT and MAPK signaling.
Our qPCR arrays deliver high precision and reproducibility, empowering researchers to uncover novel insights into the mTOR pathway’s role in health and disease.
The structures, regulatory mechanism and functions of mTORC2.
Regulatory mechanism and function of the mammalian target of rapamycin complex 1 (mTORC1). (A) The structures and regulatory mechanism of mTORC1. (B) The downstream functions of mTORC1.
Regulation of mtor complexes
mTOR exists in two distinct complexes, mTORC1 and mTORC2.
mTORC1 Regulation:
Activation: responds to nutrients, growth factors, and energy levels. Key signals include insulin signaling, amino acid and pathways such as PI3K/AKT and RAG GTPases.
Negative Regulation: Tuberous sclerosis complex (TSC) and AMPK inhibit mTORC1 under stress, low energy and hypoxia.
Function: promotes protein synthesis, lipid biosynthesis, cell growth and inhibits autophagy.
The mTOR pathway plays a pivotal role in regulating cellular and physiological processes:
Cell Growth and Proliferation: mTORC1 promotes protein synthesis through the phosphorylation of key targets such as S6 kinase and 4E-BP1.
Metabolism: regulates lipid synthesis, glucose metabolism and autophagy depending on nutrient availability.
Autophagy: inhibited under nutrient-rich conditions, activated under starvation to support survival.
Cell Survival: mTORC2 enhances AKT signaling and cytoskeletal stability.
Immune Function: modulates immune cell activation, differentiation, and stress responses.
Key components
mTORC1 (Mechanistic Target of Rapamycin Complex 1): regulates metabolism, protein synthesis, and growth.
mTORC2 (Mechanistic Target of Rapamycin Complex 2): controls cell survival, cel survival, AKT activation and cytoskeletal organization.
AMPK (AMP-Activated Protein Kinase): acts as an energy sensor, inhibits mTORC1 activity when energy is low.
Tuberous Sclerosis Complex (TSC): negative regulator, prevents excessive growth and proliferation under stress.
mTOR pathway and disease implications
Cancer: hyperactivation promotes tumor growth by enhancing protein synthesis and cell survival. mTOR inhibitors are being explored as potential treatments for various cancers.
Metabolic Disorders: dysregulated mTOR activity contributes to insulin resistance, obesity, diabetes, and cardiovascular diseases.
Neurodegenerative Diseases: impaired mTOR reduces autophagy, leading to protein accumulation in Alzheimer’s and Parkinson’s diseases.
Immune System Dysfunction: dysregulation causes autoimmune diseases, chronic inflammation, and immunodeficiency.
Therapeutic targeting of mTOR
Rapamycin: first mTOR inhibitor, used in organ transplant rejectionprevention and studied in cancer and aging-related diseases.
Dual mTOR Inhibitors: Target mTORC1 and mTORC2 for better efficacy.
Targeted Therapies: development of more specific inhibitors with fewer side effects.
The mTOR pathway is activated by nutrients, growth factors, and cellular energy status. PI3K/AKT signaling, amino acids, and insulin stimulate mTORC1, while growth factors primarily regulate mTORC2.
mTORC1 promotes protein synthesis by phosphorylating key targets such as S6 kinase (S6K1) and 4E-BP1, increasing ribosome activity and translation efficiency.
mTORC1 mainly controls protein synthesis, metabolism, and autophagy in response to nutrients and energy levels, while mTORC2 regulates cell survival, cytoskeletal organization, and AKT activation in response to growth factors.
You can review the biomarker list for the mTOR pathway in the table below to see if it matches your research focus. If the targets you need are not included, you can customize your own SignArrays® by downloading and completing our Personalized SignArrays® information file. Send it to [email protected] to get started on your project.
Saxton RA et Sabatini DM. mTOR Signaling in Growth, Metabolism, and Disease. Cell. (2017)9;168(6):960-976.
Das A et al. mTOR Signaling in Cardiometabolic Disease, Cancer, and Aging. Oxid Med Cell Longev. (2017).
Chamcheu JC et al. Role and Therapeutic Targeting of the PI3K/Akt/mTOR Signaling Pathway in Skin Cancer: A Review of Current Status and Future Trends on Natural and Synthetic Agents Therapy. Cells. (2019)31;8(8).
Wei X et al. Roles of mTOR Signaling in Tissue Regeneration. Cells. (2019)12;8(9).
Kwasnicki A et al. Involvement of mTOR signaling pathways in regulating growth and dissemination of metastatic brain tumors via EMT. Anticancer Res. (2015);35(2):689-96.
Paquette M e t al. mTOR Pathways in Cance r and Autophagy. Cancers (Basel). (2018);10(1).
Hua H e t al. Targeting mTOR for cancer therapy. J Hematol Oncol. (2019);12(1):71.