Abstract

Cancer cells support their growth and proliferation by reprogramming their metabolism in order to gain access to nutrients. Despite the heterogeneity in genetic mutations that lead to tumorigenesis, a common alteration in tumors occurs in pathways that upregulate nutrient acquisition. A central signaling pathway that controls metabolic processes is the mTOR pathway. The elucidation of the regulation and functions of mTOR can be traced to the discovery of the natural compound, rapamycin. Studies using rapamycin have unraveled the role of mTOR in the control of cell growth and metabolism. By sensing the intracellular nutrient status, mTOR orchestrates metabolic reprogramming by controlling nutrient uptake and flux through various metabolic pathways. The central role of mTOR in metabolic rewiring makes it a promising target for cancer therapy. Numerous clinical trials are ongoing to evaluate the efficacy of mTOR inhibition for cancer treatment. Rapamycin analogs have been approved to treat specific types of cancer. Since rapamycin does not fully inhibit mTOR activity, new compounds have been engineered to inhibit the catalytic activity of mTOR to more potently block its functions. Despite highly promising pre-clinical studies, early clinical trial results of these second generation mTOR inhibitors revealed increased toxicity and modest antitumor activity. The plasticity of metabolic processes and seemingly enormous capacity of malignant cells to salvage nutrients through various mechanisms make cancer therapy extremely challenging. Therefore, identifying metabolic vulnerabilities in different types of tumors would present opportunities for rational therapeutic strategies. Understanding how the different sources of nutrients are metabolized not just by the growing tumor but also by other cells from the microenvironment, in particular, immune cells, will also facilitate the design of more sophisticated and effective therapeutic regimen. In this review, we discuss the functions of mTOR in cancer metabolism that have been illuminated from pre-clinical studies. We then review key findings from clinical trials that target mTOR and the lessons we have learned from both pre-clinical and clinical studies that could provide insights on innovative therapeutic strategies, including immunotherapy to target mTOR signaling and the metabolic network in cancer.

Highlights

  • In 1956, Otto Warburg wrote that if we know how cancer cells have “damaged respiration and excessive fermentation”, we understand the origin of cancer cells [1]

  • While lapatinib downregulated mTORC2 signaling in the former tumors, only the combined ridaforolimus/lapatinib treatment was able to abrogate S6 phosphorylation in such tumors, correlating with the anti-tumor activity [253]. These findings reveal how both mTORC1 and mTORC2 signaling downregulation is critical to achieve better efficacy when both mTOR complexes are upregulated either due to amplified RTK or mutated PIK3CA

  • Over-activation of Akt has been found to be associated with many types of cancer, including HER2-amplified breast cancer and glioblastoma [288,289]. mTORC2 modulates Akt signaling by allosteric phosphorylation of Akt on Ser473. mTOR as part of mTORC2 requires the presence of its partners rictor and SIN1 to function

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Summary

Introduction

In 1956, Otto Warburg wrote that if we know how cancer cells have “damaged respiration and excessive fermentation”, we understand the origin of cancer cells [1]. Warburg proposed that the “driving force of the increased fermentation is the energy deficiency” in order to generate sufficient ATP in lieu of the defective respiration process How this happens in cancer cells was mysterious, but more modern approaches to study cancer metabolism have provided clues that may help us understand the origin of cancer and how we can eradicate them more effectively. AcCoA promotes EP300-mediated acetylation of raptor at K1097, enhancing mTORC1 activity This regulation of mTORC1 appears to be cell-type-specific, . When mTORC2 activity was disrupted genetically or pharmacologically, glutamate secretion, cystine uptake and incorporation into glutathione were enhanced This function of mTORC2 could allow highly proliferating cancer cells to utilize glutamate for TCA anaplerosis. The inhibitor of Pol I-mediated rDNA transcription (CX-5461) was combined with everolimus and was shown to synergistically increase the survival of mice with a Myc-driven lymphoma [70]

Glucose Metabolism
Lipid Metabolism
Pentose Phosphate Pathway and Nucleotide Synthesis
Targeting the mTOR Pathway in Cancer
Rapalogs
Co-targeting mTORC1 and Growth Factor Signaling
Targeting mTORC2 Signaling
RapaLink1
Co-targeting mTOR and Metabolism
3.10. Other Inhibitors of the mTOR Pathway
3.11. Resistance Mechanisms and Other Therapeutic Opportunities
Findings
Conclusions
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