Inhibitory effect of mutant cytosine deaminase D314A against human colon cancer cells
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3872/j.issn.1007-385X.2009.06.008
   		
        
        	
        		- VernacularTitle:胞嘧啶脱氨酶基因突变体D314A对人结肠癌细胞的抑制作用
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Maocai SUN
			        		
			        		;
		        		
		        		
		        		
			        		Yiming HUANG
			        		
			        		;
		        		
		        		
		        		
			        		Zhengcai ZHU
			        		
			        		;
		        		
		        		
		        		
			        		Jianping WANG
			        		
			        		;
		        		
		        		
		        		
			        		Lizong SHEN
			        		
			        		;
		        		
		        		
		        		
			        		Wenxi WU
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		cytosine deaminase;
			        		
			        		
			        		
				        		site-directed mutation;
			        		
			        		
			        		
				        		suicide gene therapy;
			        		
			        		
			        		
				        		colon neoplasms
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Cancer Biotherapy
	            		
	            		 2009;16(6):595-599
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Objective:To construct a mutant D314A of Escherichia coli cytosine deaminase (EC-CD, substitution of an alanine (A) for the aspartic acid (D) at position 314 of cytosine deaminase) and investigate its antitumor effect. Methods: Eukaryotic expression plasmid containing EC-CD gene (pcDNA3.1-CD~(wt)) was constructed, and the mutant pcDNA3.1-CD~(D314A) plasmid, with aspartic acid (D) at position 314 of EC-CD gene substituted by alanine (A) (EC-CD~(D314A)), was established by site-directed mutation. EC-CD~(wt) and EC-CD~(D314A) were transfected into human colon cancer cell line LoVo via Lipofectamine~(tm) 2000, and positive LoVo-CD~(wt) and LoVo-CD~(D314A) cells stably expressing corresponding genes were selected by G418. The cytotoxicity and bystander effects of EC-CD and EC-CD~(D314A) genes on LoVo cells were e-valuated by MTT assay. Results: The mutant D314A was confirmed by sequence analysis. EC-CD and EC-CD~(D314A) mRNA were expressed after transfected into LoVo cells. The IC_(50) of Lovo-CD~(D314A) cells was (85.13±0.60) mmol/L, which was significantly lower than that of LoVo-CD~(wt) cells ([689.76±0.45] μmol/L, P=0.000). Bystander effect assay showed that, when at the ratio of 30%, the survival rates of LoVo-CD~(wt) cells and Lovo-CD~(D314A) cells were (48.5±0.49)% and (17.3±0.40) % (P = 0.000), respectively. Conclusion: Mutatant EC-CD gene (EC-CD~(D314A)) has a significantly in-creased antitumor effect on LoVo cells compared with wild type EG-CD gene, and it may become a new candidate gene for tumor gene therapy.