Abstract #0844
            Detection of Acute Response to Proteasome Inhibitor Treatment in Mouse Colorectal Tumour Models Using Amide Proton Transfer (APT) Magnetic Resonance Imaging
                      Yanan Zhu                     1                    , Rajiv Ramasawmy                     1                    , Sean 						Peter Johnson                     2                    , Valerie Taylor                     1                    , 						Barbara Pedley                     2                    , Allison Berger                     3                    , 						Nibedita Chattopadhyay                     3                    , Daniel Bradley                     4                    , 						Mark Lythgoe                     1                    , and Simon Walker-Samuel                     1          
            
            1
           
           UCL Centre for Advanced Biomedical Imaging, 
						University College London, London, Greater London, 
						United Kingdom,
           
            2
           
           UCL 
						Cancer Institute, University College London, Greater 
						London, United Kingdom,
           
            3
           
           Cancer 
						Pharmacology Takeda Pharmaceutical International 
						Corporation, MA, United States,
           
            4
           
           The 
						Biomedical Imaging Group, Takeda Pharmaceutical 
						International Corporation, MA, United States
          
            
          In this study, amide proton transfer (APT) imaging was 
						used to assess the acute response of a colorectal 
						xenograft model to proteosome inhibitor therapy (ixazomib). 
						Tumour apparent diffusion coefficient (ADC), T1, and T2 
						were also acquired, alongside 31P magnetic resonance 
						spectroscopy data. Treated mice showed an inhibited 
						tumour growth rate, decreased APT and increased ADC, 
						compared with control mice, which could be due to 
						changes in protein homeostasis as a result of proteasome 
						inhibition by the drug.
         
				
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