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Global profiling strategies for mapping dysregulated metabolic pathways in cancer.

Cell metabolism (2012-10-16)
Daniel I Benjamin, Benjamin F Cravatt, Daniel K Nomura
ZUSAMMENFASSUNG

Cancer cells possess fundamentally altered metabolism that provides a foundation to support tumorigenicity and malignancy. Our understanding of the biochemical underpinnings of cancer has benefited from the integrated utilization of large-scale profiling platforms (e.g., genomics, proteomics, and metabolomics), which, together, can provide a global assessment of how enzymes and their parent metabolic networks become altered in cancer to fuel tumor growth. This review presents several examples of how these integrated platforms have yielded fundamental insights into dysregulated metabolism in cancer. We will also discuss questions and challenges that must be addressed to more completely describe, and eventually control, the diverse metabolic pathways that support tumorigenesis.

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Sigma-Aldrich
Pyruvat-Kinase aus Kaninchenmuskel, Type III, lyophilized powder, 350-600 units/mg protein
Sigma-Aldrich
Pyruvat-Kinase aus Kaninchenmuskel, Type II, ammonium sulfate suspension, 350-600 units/mg protein
Sigma-Aldrich
Pyruvat-Kinase aus Kaninchenmuskel, Type VII, buffered aqueous glycerol solution, 350-600 units/mg protein