| 
        
        
              
                |  2011/09/14 | 
               
               
                | LHD – PUFA Have Potential As Anti-Cancer Molecules   | 
               
               
                
                    Das UN, Madhavi N. Effect of polyunsaturated fatty acids on drug-sensitive and resistant tumor cells in vitro. Lipids Health Dis. 2011 Sep 14;10(1):159.  
                    | 
               
              
                Previous studies showed that gamma-linolenic acid (GLA, 18: 3 omega-6), arachidonic acid (AA, 20:4 omega -6), eicosapentaenoic acid (EPA, 20: 5 omega -3) and docosahexaenoic acid (DHA, 22:6 omega -3) have selective tumoricidal action. In the present study, it was observed that dihomo-gamma-linolenic acid (DGLA) and AA, EPA and DHA have cytotoxic action on both vincristine-sensitive (KB-3-1) and resistant (KB-ChR-8-5) cancer cells in vitro that appeared to be a free-radical dependent process but not due to the formation of prostaglandins, leukotrienes and thromboxanes.  
 
Uptake of vincristine and fatty acids was higher while their efflux was lower in KB-3-1 cells compared with KB-ChR-8-5 cells, suggesting that drug resistant cells have an effective efflux pump. GLA, DGLA, AA, EPA and DHA enhanced the uptake and decreased efflux in both drug-sensitive and drug-resistant cells and augmented the susceptibility of tumor cells especially, of drug-resistant cells to the cytotoxic action of vincristine.  
 
These results suggest that certain polyunsaturated fatty acids have tumoricidal action and are capable of enhancing the cytotoxic action of anti-cancer drugs specifically, on drug-resistant cells by enhancing drug uptake and reducing its efflux.  
 
Thus, polyunsaturated fatty acids either by themselves or in combination with chemotherapeutic drugs have the potential as anti-cancer molecules. 
 
PMID: 21917129 
 
See following website for full manuscript 
 | 
               
              
                | Source: 
								http://www.lipidworld.com/content/10/1/159/abstract
												 | 
               
 
        
                   
                        |