Expression of Exogenous r-Interferon Genes in Human HepatoceUuIar Carcinoma Cells Following Retroviral Transduction
	    		
		   		
	    	
    	
    	
   		
        
        	
        		- VernacularTitle:逆转录病毒载体介导的?-干扰素基因在人肝癌细胞中的表达研究
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Shubing QIAN
			        		
			        		;
		        		
		        		
		        		
			        		Tengfei ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Liang HU
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		retroviral vector;
			        		
			        		
			        		
				        		7-Inteferon;
			        		
			        		
			        		
				        		hepatocellular carcinoma;
			        		
			        		
			        		
				        		HIA class I molecule
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Cancer Biotherapy
	            		
	            		 1995;0(02):-
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Retroviral vector pLXSN was employed to introduce human r-Interferon (IFN-?) gene into four human hepa-tocellular carcinoma cell lines (HCC). The G418-resistant colonies were isolated and cloned. PCR and RT-PCR analysis indicated that the integration and expression of IFN-? gene was shown only in the transduced cells. Using a bioassay method, we found that all genetically modified HCC cells can secrete varied amount of IFN-?. The results of flow cytome-try showed that the cell surface expression of HLA class I molecules significandy increased following transduction. Moreover , we firsdy indicated that the increase in the expression of one specific HLA class I antigen, HLA-A2, was almost in the same magnitude as that of the total HLA class I molecules after transduction with IFN-r gene.