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Transfer of Manipulated Tumor-associated Neutrophils into Tumor-Bearing Mice to Study their Angiogenic Potential In Vivo
Published on: July 20, 2019
Nitric oxide and tumor metabolic reprogramming
Laura M López-Sánchez1, Enrique Aranda2, Antonio Rodríguez-Ariza2
1Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Av. Menéndez Pidal s/n, E14004 Córdoba, Spain; Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Av. Monforte de Lemos, 3-5, E 28029 Madrid, Spain.
Abstract:
Nitric oxide (NO) has been highlighted as an important agent in tumor processes. However, a complete understanding of the mechanisms by which this simple diatomic molecule contributes in tumorigenesis is lacking. Evidence is rapidly accumulating that metabolic reprogramming is a major new aspect of NO biology and this review is aimed to summarize recent research progress on this novel feature that expands the complex and multifaceted role of NO in cancer. Therefore, we discuss how NO may influence glucose and glutamine utilization by tumor cells, and its participation in the regulation of mitochondrial function and dynamics, that is an important mechanism through which cancer cells reprogram their metabolism to meet the biosynthetic needs of rapid proliferation. Finally, we also discuss the NO-related metabolic rewiring involved in the modification of the tumor microenvironment to support cancer invasion and the escape from immune system-mediated recognition. Protein S-nitrosylation appears as a common mechanism by which NO signaling reprograms metabolism. Hence, future research is needed on dysregulated S-nitrosylation/denitrosylation in cancer to comprehend the NO-induced metabolic changes in tumor cells and the role of NO in the metabolic crosstalk within tumor microenvironment.
Insights
Nitric oxide (NO) reprograms cancer cell metabolism, influencing nutrient use and mitochondrial function. This metabolic rewiring aids tumor growth, invasion, and immune evasion, with protein S-nitrosylation as a key mechanism.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Metabolism
Background:
- Nitric oxide (NO) plays a complex role in tumor progression.
- Mechanisms linking NO to tumorigenesis, particularly metabolic reprogramming, require further elucidation.
Purpose of the Study:
- To review recent advances in understanding NO's role in cancer metabolic reprogramming.
- To highlight how NO influences cancer cell metabolism and the tumor microenvironment.
Main Methods:
- Literature review of recent research on NO and cancer metabolism.
- Discussion of NO's impact on glucose/glutamine utilization, mitochondrial function, and S-nitrosylation.
Main Results:
- NO influences glucose and glutamine metabolism in tumor cells.
- NO regulates mitochondrial function and dynamics, supporting cancer proliferation.
- NO-mediated metabolic changes affect the tumor microenvironment, promoting invasion and immune escape.
Conclusions:
- Metabolic reprogramming is a critical aspect of NO's multifaceted role in cancer.
- Protein S-nitrosylation is a central mechanism for NO-induced metabolic alterations.
- Further research into S-nitrosylation/denitrosylation is crucial for understanding NO's impact on cancer metabolism and the tumor microenvironment.
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