Fang, H.Y.* ; Stangl, S.* ; Marcazzan, S. ; Carvalho, M.J.B.* ; Baumeister, T.* ; Anand, A.* ; Strangmann, J.* ; Huspenina, J.S.* ; Wang, T.C.* ; Schmid, R.M.* ; Feith, M.* ; Friess, H.* ; Ntziachristos, V. ; Multhoff, G.* ; Gorpas, D. ; Quante, M.*
     
 
    
        
Targeted Hsp70 fluorescence molecular endoscopy detects dysplasia in Barrett's esophagus.
    
    
        
    
    
        
        Eur. J. Nucl. Med. Mol. Imaging, DOI: 10.1007/s00259-021-05582-y (2021)
    
    
    
		
		
			
				PURPOSE: The incidence of esophageal adenocarcinoma (EAC) has been increasing for decades without significant improvements in treatment. Barrett's esophagus (BE) is best established risk factor for EAC, but current surveillance with random biopsies cannot predict progression to cancer in most BE patients due to the low sensitivity and specificity of high-definition white light endoscopy. METHODS: Here, we evaluated the membrane-bound highly specific Hsp70-specific contrast agent Tumor-Penetrating Peptide (Hsp70-TPP) in guided fluorescence molecular endoscopy biopsy. RESULTS: Hsp70 was significantly overexpressed as determined by IHC in dysplasia and EAC compared with non-dysplastic BE in patient samples (n = 12) and in high-grade dysplastic lesions in a transgenic (L2-IL1b) mouse model of BE. In time-lapse microscopy, Hsp70-TPP was rapidly taken up and internalized  by human BE dysplastic patient-derived organoids. Flexible fluorescence endoscopy of the BE mouse model allowed a specific detection of Hsp70-TPP-Cy5.5 that corresponded closely with the degree of dysplasia but not BE. Ex vivo application of Hsp70-TPP-Cy5.5 to freshly resected whole human EAC specimens revealed a high (> 4) tumor-to-background ratio and a specific detection of previously undetected tumor infiltrations. CONCLUSION: In summary, these findings suggest that Hsp70-targeted imaging using fluorescently labeled TPP peptide may improve tumor surveillance in BE patients.
			
			
				
			
		 
		
			
				
					
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
    
        Typ der Hochschulschrift
        
    
 
    
        Herausgeber
        
    
    
        Schlagwörter
        Barrett Esophagus ; Esophageal Adenocarcinoma ; Fluorescence Molecular Endoscopy ; Hsp70  ; Surveillance Strategies; Heat-shock Proteins; Plasma-membrane Expression; Heat-shock-protein-70 Hsp70; Tumor-cells; Mouse Model; Adenocarcinoma; Surface; Risk
    
 
    
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        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2021
    
 
    
        Prepublished im Jahr 
        
    
 
    
        HGF-Berichtsjahr
        2021
    
 
    
    
        ISSN (print) / ISBN
        1619-7070
    
 
    
        e-ISSN
        1432-105X
    
 
    
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            Verlag
            Springer
        
 
        
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            One New York Plaza, Suite 4600, New York, Ny, United States
        
 
	
        
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        Peer reviewed
    
 
     
    
        POF Topic(s)
        30205 - Bioengineering and Digital Health
    
 
    
        Forschungsfeld(er)
        Enabling and Novel Technologies
    
 
    
        PSP-Element(e)
        G-505500-001
    
 
    
        Förderungen
        Deutsche Forschungsgemeinschaft
    
 
    
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        Erfassungsdatum
        2021-12-22