In Vitro and In Vivo Imaging of Prostate Cancer Angiogenesis Using Anti-Vascular Endothelial Growth Factor Receptor 2 Antibody-Conjugated Quantum Dot.
	    		
		   		
		   			
		   		
	    	
    	- Author:
	        		
		        		
		        		
			        		Haejin KWON
			        		
			        		
			        		
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			        		Jiyeon LEE
			        		
			        		;
		        		
		        		
		        		
			        		Rita SONG
			        		
			        		;
		        		
		        		
		        		
			        		Sung Il HWANG
			        		
			        		;
		        		
		        		
		        		
			        		Junghan LEE
			        		
			        		;
		        		
		        		
		        		
			        		Young Hwa KIM
			        		
			        		;
		        		
		        		
		        		
			        		Hak Jong LEE
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Original Article ; Research Support, Non-U.S. Gov't
 - Keywords: Quantum dot; VEGFR2; Angiogenesis; Prostate cancer; Near infrared
 - MeSH: Animals; Carbodiimides/pharmacology; Cell Line, Tumor; Disease Models, Animal; Electrophoresis, Agar Gel; Fluorescence; Male; Mice; Mice, Nude; Microscopy, Confocal; Neovascularization, Pathologic/*pathology; Prostatic Neoplasms/*pathology; *Quantum Dots; Succinimides/pharmacology; Transplantation, Heterologous; Vascular Endothelial Growth Factor Receptor-2/*antagonists & inhibitors
 - From:Korean Journal of Radiology 2013;14(1):30-37
 - CountryRepublic of Korea
 - Language:English
 - Abstract: OBJECTIVE: Authors aimed to determine the targeting ability of vascular endothelial growth factor receptor 2 (VEGFR2)-conjugated quantum dots (QDs) in vitro, and apply it for a xenograft prostate cancer mouse model. MATERIALS AND METHODS: Conjugation reaction of QDs was performed by using the N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (EDC) and sulfo-(N-hydroxysulfosuccinimide) (Sulfo-NHS). The human umbilical vein cord endothelial cells (HUVECs) were incubated with QDs, conjugated with antiVGFR2, to see a specific binding in vitro. Fluorescent cell images were taken by a confocal microscope. The human prostate cancer cells (PC3) were injected to five nude mice on hind limbs to make the xenograft tumor model. QD-antiVEGFR2 antibody complex was injected into the tumor model and fluorescence measurements were performed at 1, 4, 9, 12, 15, and 24 hours after the injection. RESULTS: The specific interaction between HUVECs and QD-antiVEGFR2 antibody was clearly shown in vitro. The in vivo fluorescence image disclosed that there was an increased signal of tumor, 12 hours after the injection of QDs. CONCLUSION: By showing endothelial cells binding with QDs-antiVEGFR2 antibodyand an experimental application of the antibody for VEGFR2 imaging in the prostate cancer xenograft mouse model, we suggests that the antibody-conjugated QDs can be a potential imaging tool for angiogenesis of the cancer.
 
            