Abstract #0849
            Metabolic subgrouping of breast cancer using HR MAS MRS and hierarchical cluster analysis; correlation with molecular subtypes
                      Leslie R. Euceda                     1,2                    , Tonje H. Haukaas                     1,2                    , 						Guro F. Giskedegrd                     1                    , Marit Krohn                     2,3                    , 						Ellen Schlichting                     4                    , Rolf Kresen                     2,4                    , 						Sandra Nyberg                     2,3                    , Kristine Kleivi Sahlberg                     2,3                    , 						Anne-Lise Brresen-Dale                     2,3                    , and Tone F. 						Bathen                     1,2          
            
            1
           
           Department of Circulation and Medical 
						Imaging, Faculty of Medicine, NTNU, Trondheim, Norway,
           
            2
           
           K.G. 
						Jebsen Center for Breast Cancer Research, Institute of 
						Clinical Medicine, Faculty of Medicine, University of 
						Oslo, Oslo, Norway,
           
            3
           
           Department 
						of Genetics, Institute for Cancer Research Oslo 
						University Hospital, The Norwegian Radium Hospital, 
						Norway,
           
            4
           
           Department 
						of Surgery, Oslo University Hospital, Ullevl, Oslo, 
						Norway
          
            
          Metabolic subgroups resulting from hierarchical 
						clustering of MR metabolic profiles from a large cohort 
						of breast tumor biopsies were combined with data from 
						gene expression and reverse phased protein arrays to 
						search for any relationship between metabolic profiles 
						and molecular subtypes. No such relationships were 
						established, which might make it possible for a more 
						refined division of subtypes into subclasses based on 
						metabolic differences. Bridging information from several 
						molecular levels in the same tumor may improve our 
						knowledge about various classes of breast cancer that 
						may contribute to personalized treatment.
         
				
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