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Abstract #0177

Assessment of Glutamine Metabolism in Mammary Tumor Recurrence Using 13C MRS

MAGNA25Dania Daye1, 2, Suzanne Wehrli3, George Belka4, Anthony Mancuso5, Chris Sterner6, Mitchell Schnall5, Lewis Chodosh

1Abramson Family Cancer Research Institute, Perelman School of Medicine at the University of Pennsylvania , Philadelphia, PA, United States; 2Bioengineering Graduate Group, University of Pennsylvania, Philadelphia, PA, United States; 3Children's Hospital of Philadelphia; 4Department of Cancer Biology , Perelman School of Medicine at the University of Pennsylvania; 5Department of Radiology, Perelman School of Medicine at the University of Pennsylvania; 6Department of Cancer Biology, Perelman School of Medicine at the University of Pennsylvania

Tumor recurrence represents the principal cause of death from breast cancer. Despite being a critical clinical problem, little is known about the cellular and molecular mechanisms underlying tumor recurrence. Our laboratory has developed an inducible transgenic mouse model that accurately reproduces key features of the natural history of human breast cancer progression including tumor recurrence. Dysregulated metabolism has been shown to be key feature of tumorigenesis. To date, very little is know about the association between changes in metabolism and cancer recurrence. In this study, we investigate the role of 13C-glutamine as a potential breast cancer progression marker using MRS.

Keywords

accurately acid acorn addition allow assessed assessment association bearing bioengineering biology breast cancer carbon catalyzes cause cell cells cellular clinical commonly component computation computed conditionally conditions conducted considered contributing critical death degrees described despite determinant determinants determined developed development diagnosed display dormancy enable enzyme exhibit express expression extraction family feature features find flash frozen gene gland glutamate goal graduate growth history hospital human identify improvements included indicate inducible infusion institute integrals investigate involved known labeled laboratory lead leading limiting little major malignancy mammary marker mechanisms medicine metabolic metabolism metastasis mice might minutes model molecular moody mouse nitrogen nuts particular particularly pathways peak period potential prediction preliminary prevention previously primary principal probe profile progress progression quantification quantify radiology recurrence recurrent related represents reproduces required reveals role sample school significance software solution spectra spectral spectrometer speculate statistical step sterner student substantial tail treatment tumor tumors ultimately underlying understanding vein vitro wide women worldwide