Expressions of estrogen receptor subtypes and c-met proto-oncogene in endometrial carcinoma and their correlation 
	    		
		   		
	    	
    	
    	
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Yue-Ling WANG
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		
		        		
		        		
		        		
    Author Information Author Information
 
			        		
			        		
			        			1. Department of Obstetrics and Gynecology
 
 
- Publication Type:Journal Article
- Keywords:
        			
	        			
	        				
	        				
			        		
				        		C-met proto-oncogene;
			        		
			        		
			        		
				        		Endometrial carcinoma;
			        		
			        		
			        		
				        		Estrogen receptor α;
			        		
			        		
			        		
				        		Estrogen receptor β
			        		
			        		
	        			
        			
        		
- From:Academic Journal of Xi'an Jiaotong University
	            		
	            		 2010;22(1):54-58
	            	
            	
- CountryChina
- Language:Chinese
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		        	Abstract:
			       	
			       		
				        
				        	 Objective: To investigate the expressions of estrogen receptor (ER) subtypes and c-met proto-oncogene in human endometrial carcinomas and to assess the clinical significance of ER and c-met in this carcinoma. Methods: Reverse transcription PCR (RT-PCR) was used to detect the expressions of ERα, ERβ and c-met proto-oncogene mRNA in 30 samples of endometrial carcinoma and 11 samples of normal endometrium. Results: The expression of ERα in endometrial carcinoma (0.70±0.40) was significantly reduced in comparison to that in normal endometrium (1.14±0.56, P<0.05). A similar finding was made for the expression of ERβ in carcinoma (0.24±0.18) versus normal tissues (0.48±0.20, P<0.05). In contrast, c-met mRNA expression was increased in endometrial carcinoma (1.45±0.72) compared to that in normal endometrium (0.42±0.31, P<0.01). A decrease tendency of the expression of ERα was also found from Stage I (0.82±0.41) to a more severe Stag II-III of endometrial carcinoma (0.42±0.17, P<0.05). The analysis of ERα and ERβ mRNA revealed a decrease tendency from shallow to deep invasion of the uterine muscles (P<0.05). We found that the expressions of ERα and ERβ were negatively correlated with c-met proto-oncogene with a coefficient correlation of -0.63 (P<0.01) and -0.32 (P<0.05), respectively. Conclusion: ERα and ERβ are both involved in mutagenic action of carcinogen. C-met proto-oncogene plays an important role in the carcinogenesis and development of endometrial carcinoma. C-met and ER expressions show a negative correlation in the development of endometrial carcinoma.