Effect of parthenolide on proliferation and migration of MCF-7 breast cancer cells by targeting the c-myc G-quadruplex
	    		
		   		
		   			
		   		
	    	
    	- VernacularTitle:小白菊内酯通过靶向c-myc G-四链体抑制乳腺癌细胞增殖和迁移
 - Author:
	        		
		        		
		        		
			        		Yu-qing WANG
			        		
			        		
			        		
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			        		Yue GAO
			        		
			        		
			        		
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			        		Rong WEI
			        		
			        		
			        		
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			        		Rang LI
			        		
			        		
			        		
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			        		Pei-min HUANG
			        		
			        		
			        		
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			        		Chun-rong HUANG
			        		
			        		
			        		
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			        		Chao ZHANG
			        		
			        		
			        		
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			        		Yi-wen TAO
			        		
			        		
			        		
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			        		Jian-ye ZHANG
			        		
			        		
			        		
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			        		Author Information
			        		
 - Publication Type:Research Article
 - Keywords: parthenolide; G-quadruplex; breast cancer; proliferation; migration
 - From: Acta Pharmaceutica Sinica 2020;55(7):1622-1626
 - CountryChina
 - Language:Chinese
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		        	Abstract:
			       	
			       		
				        
				        	 This research investigated the effect of parthenolide on the proliferation and migration of human breast cancer cells and explored the molecular mechanism of that effect
. Surface plasmon resonance and fluorescence resonance energy transfer melting were used to detect the binding and stabilizing ability of PTL and G-quadruplex. MTT assays were used to determine the effect of PTL on the proliferation of MCF-7 breast cancer cells. A wound healing assay was performed to detect the migration of MCF-7. The results indicate that PTL shows good binding and stabilizing activities with c-myc G-quadruplex with aK D = 13.1 μmol·L-1. PTL inhibited the proliferation of MCF-7 cells with an IC50 of 21.3 μmol·L-1 (24 h), 14.5 μmol·L-1 (48 h) and 9.1 μmol·L-1 (72 h). PTL inhibited MCF-7 breast cancer cell proliferation and migration and down-regulated the transcription and expression level of c-myc by targeting G-quadruplex. 
            