Saul Carcamo University College of London

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Presentation transcript:

A Novel Mechanism for Regulating Glycolysis and Glutaminolysis During the Cell Cycle Saul Carcamo University College of London Professor Sir Salvador Moncada

Production of Energy

Cells are able to upregulate glycolysis due to the activity of glycolysis-promoting enzyme PFKFB3

Cells are able to upregulate glutaminolysis due to the activity of the promoting enzyme GLS1 Gls1

Cell Division

Cell cycle.

Ubiquination

The APC/C and SFC play an essential role in mitosis through the degradation of cell cycle proteins.

Methods Cell Synchronization

APC/C-Cdh1 and SFC: linking glycolysis and glutaminolysis to cell proliferation

APC/C-Cdh1 and SFC: linking glycolysis and glutaminolysis to cell proliferation

Conclusion and Impact The accelerated utilization of glucose and glutamine is regulated by PFKFB3 and GLS1 respectively This metabolic programming contributes to the rapid production of biosynthetic precursors, such as nucleotides, carbohydrates, amino acids, and fatty acids, which are required for cell proliferation Given their timely and selective targeting of substrates, APC/CCdh1 and SCF coordinate global metabolism networks with the cell cycle. It will be interesting to determine whether nonmalignant cells also use these mechanisms to regulate energy production and macromolecular precursor biosynthesis. Further investigation will provide important information about the contribution of metabolic pathways to cell growth and malignancy, as well as the specific metabolic features used by tumor cells.