PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
11306488-3	2001	To explore the role of caspases in cancer cell apoptosis induced by selenium, we examined the involvement of these molecules in the death of the DU-145 human prostate carcinoma cells induced by methylseleninic acid (MSeA), a novel penultimate precursor of the putative critical anticancer metabolite CH3SeH.	Selenium	68-76	caspase 8	Homo sapiens	23-31	
19940991-11	2010	CONCLUSION: The present findings demonstrate that Se-induced apoptosis in carcinoma cells is basically a caspase-dependent process involving complicated mechanisms.	Selenium	50-52	caspase 8	Homo sapiens	105-112	
12432279-6	2002	Selenium upregulation of DR5 was coupled with caspase 8 activation and Bid cleavage thereby suggesting the existence of a potential cross-talk between the DR5 and the mitochondrial pathways.	Selenium	0-8	caspase 8	Homo sapiens	46-55	
19189638-0	2008	Role of caspases in 5-FU and selenium-induced growth inhibition of colorectal cancer cells.	Selenium	29-37	caspase 8	Homo sapiens	8-16	
17970047-7	2007	Selenium, on the other hand, increased the expression of FADD, a key adaptor molecule responsible for recruitment of caspase-8 to the Fas oligomer.	Selenium	0-8	caspase 8	Homo sapiens	117-126	
17970047-8	2007	The significance of the above changes was confirmed by the detection of considerably more caspase-8 in both the Fas or FADD immunoprecipitate obtained from cells treated with the doxorubicin/selenium combination.	Selenium	191-199	caspase 8	Homo sapiens	90-99