Contribution of eukaryotic initiation factor-4E inhibition to heparanase expression and activity in human colon adenocarcinoma cell line LS-174T.
- Author:
	        		
		        		
		        		
			        		Yu-jie YANG
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Ya-li ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Zhuo-sheng LAI
			        		
			        		;
		        		
		        		
		        		
			        		Ji-de WANG
			        		
			        		;
		        		
		        		
		        		
			        		Bao-ping WU
			        		
			        		;
		        		
		        		
		        		
			        		Ya-dong WANG
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Journal Article
 - MeSH: Adenocarcinoma; enzymology; pathology; Cell Line, Tumor; Colonic Neoplasms; enzymology; pathology; Eukaryotic Initiation Factor-4E; antagonists & inhibitors; genetics; physiology; Glucuronidase; metabolism; Humans; Neoplasm Invasiveness
 - From: Chinese Journal of Oncology 2003;25(6):542-545
 - CountryChina
 - Language:Chinese
 - 
		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVETo determine whether the eukaryotic initiation factor-4E (eIF-4E) is involved in the cap-dependent translational regulation of heparanase and study the correlation between heparanase expression and metastatic potential of LS-174T cells.
METHODSThe protein and mRNA levels of inhibited eIF-4E were tested by Western blot and RT-PCR. Heparanase activity was defined as the ability to degrade high molecular weight (40-100 000) radiolabeled ((35)S) heparan sulfate (HS) substrate into low molecular weight (5-15 000) HS fragments. The invasive potential of tumor cells in vitro was observed by Matrigel invasion assay system.
RESULTSThe 20-mer antisense oligonucleotide (asODN) against eIF-4E specifically and significantly inhibited eIF-4E expression at both transcriptional and translational levels. The expression and the activity of heparanase were effectively lowered, which further decreased the invasive potential of LS-174T.
CONCLUSIONeIF-4E, probably being involved in translational regulation of heparanase in colon adenocarcinoma cell line LS-174T, can be a particularly interesting target for heparanase regulation, based on of its critical function.
 
            