CRISPR-Cas9: A method for establishing rat models of drug metabolism and pharmacokinetics.
	    		
		   		
		   			
		   		
	    	
    	 
    	10.1016/j.apsb.2021.01.007
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Jian LU
			        		
			        		
			        		
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			        		Jie LIU
			        		
			        		
			        		
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			        		Yuanqing GUO
			        		
			        		
			        		
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			        		Yuanjin ZHANG
			        		
			        		
			        		
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			        		Yeye XU
			        		
			        		
			        		
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			        		;
		        		
		        		
		        		
			        		Xin WANG
			        		
			        		
			        		
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			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Changning Maternity and Infant Health Hospital, East China Normal University, Shanghai 200051, China.
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Review
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		AAV, adeno-associated virus;
			        		
			        		
			        		
				        		ADMET, absorption, distribution, metabolism, excretion and toxicity;
			        		
			        		
			        		
				        		Animal model;
			        		
			        		
			        		
				        		BSEP, bile salt export pump;
			        		
			        		
			        		
				        		CRISPR-Cas, clustered regularly interspaced short palindromic repeats-CRISPR-associated;
			        		
			        		
			        		
				        		CRISPR-Cas9;
			        		
			        		
			        		
				        		DDI, drug–drug interaction;
			        		
			        		
			        		
				        		DMPK, drug metabolism and pharmacokinetics;
			        		
			        		
			        		
				        		DSB, double-strand break;
			        		
			        		
			        		
				        		Drug metabolism;
			        		
			        		
			        		
				        		Gene editing;
			        		
			        		
			        		
				        		HBV, hepatitis B virus;
			        		
			        		
			        		
				        		HDR, homology directed repair;
			        		
			        		
			        		
				        		HIV, human immunodeficiency virus;
			        		
			        		
			        		
				        		HPV, human papillomaviruses;
			        		
			        		
			        		
				        		KO, knockout;
			        		
			        		
			        		
				        		NCBI, National Center for Biotechnology Information;
			        		
			        		
			        		
				        		NHEJ, non-homologous end joining;
			        		
			        		
			        		
				        		OATP1B, organic anion transporting polypeptides 1B;
			        		
			        		
			        		
				        		OTS, off-target site;
			        		
			        		
			        		
				        		PAM, protospacer-associated motif;
			        		
			        		
			        		
				        		Pharmacokinetics;
			        		
			        		
			        		
				        		RNP, ribonucleoprotein;
			        		
			        		
			        		
				        		SD, Sprague–Dawley;
			        		
			        		
			        		
				        		SREBP-2, sterol regulatory element-binding protein 2;
			        		
			        		
			        		
				        		T7E I, T7 endonuclease I;
			        		
			        		
			        		
				        		TALE, transcriptional activator-like effector;
			        		
			        		
			        		
				        		TALEN, transcriptional activators like effector nucleases;
			        		
			        		
			        		
				        		WT, wild-type;
			        		
			        		
			        		
				        		ZFN, zinc finger nucleases;
			        		
			        		
			        		
				        		crRNAs, CRISPR RNAs;
			        		
			        		
			        		
				        		pre-crRNA, pre-CRISPR RNA;
			        		
			        		
			        		
				        		sgRNA, single guide RNA;
			        		
			        		
			        		
				        		tracRNA, trans-activating crRNA
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Acta Pharmaceutica Sinica B
	            		
	            		 2021;11(10):2973-2982
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:English
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	The 2020 Nobel Prize in Chemistry recognized CRISPR-Cas9, a super-selective and precise gene editing tool. CRISPR-Cas9 has an obvious advantage in editing multiple genes in the same cell, and presents great potential in disease treatment and animal model construction. In recent years, CRISPR-Cas9 has been used to establish a series of rat models of drug metabolism and pharmacokinetics (DMPK), such as