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						 Cholesterol 
						pill boosts cancer immunotherapy, at least in mice 
			
   
            
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		[March 17, 2016] 
		LONDON (Reuters) - Tweaking 
		cholesterol levels with a simple pill may boost the effectiveness of new 
		immunotherapy drugs that are starting to revolutionize the treatment of 
		cancers, experiments in mice suggest. 
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			 Two new drugs from Bristol-Myers Squibb and Merck, Opdivo and 
			Keytruda, help the body's immune system fight tumors and are already 
			being used to fight lung cancer, kidney cancer and melanoma. 
			 
			But such so-called checkpoint inhibitors, which are also being 
			developed by Roche, AstraZeneca and Pfizer, do not work for all 
			patients, prompting scientists to search for improvements. 
			 
			One option could be to modify cholesterol levels, since this can 
			increase the anti-cancer activity of immune cells known as killer T 
			cells, Chenqi Xu of the Chinese Academy of Sciences and colleagues 
			reported in the journal Nature on Thursday. 
			
			  
			In particular, they found that adding the drug avasimibe to 
			checkpoint drugs that block a protein called Programmed Death 
			receptor (PD-1) improved tumor inhibition and increased survival in 
			mice. 
			 
			"These data show that avasimibe and anti-PD-1 act through different 
			pathways and have additive effects in cancer immunotherapy," they 
			wrote. 
			 
			Avasimibe was originally developed by Pfizer, which at one stage saw 
			it as a potential contender to succeed its blockbuster cholesterol 
			fighter Lipitor. But it was dropped from development after failing 
			to treat cardiovascular disease as well as hoped. 
			
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			Nonetheless, it can still be used in clinical trials and it has the 
			advantage of being administered as a pill. 
			 
			Michael Dustin of the University of Oxford, who wrote an 
			accompanying comment about the latest research, said it was 
			"exciting to speculate" that doctors might one day be able to 
			prescribe a pill to boost cancer immunotherapy. 
			 
			(Reporting by Ben Hirschler; Editing by Greg Mahlich) 
			[© 2016 Thomson Reuters. All rights 
				reserved.] Copyright 2016 Reuters. All rights reserved. This material may not be published, 
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