PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
17252557-0	2007	Inhibition of the epidermal growth factor receptor enhances castration-induced prostate involution and reduces testosterone-stimulated prostate growth in adult rats.	Testosterone	111-123	epidermal growth factor receptor	Rattus norvegicus	18-50	
17252557-4	2007	RESULTS: Both castration alone and testosterone treatment in castrated animals increased the mRNA and protein levels of EGFR and phospho-EGFR in the ventral prostate.	Testosterone	35-47	epidermal growth factor receptor	Rattus norvegicus	120-124	
17252557-4	2007	RESULTS: Both castration alone and testosterone treatment in castrated animals increased the mRNA and protein levels of EGFR and phospho-EGFR in the ventral prostate.	Testosterone	35-47	epidermal growth factor receptor	Rattus norvegicus	137-141	
17252557-5	2007	Inhibition of EGFR during castration and during testosterone-stimulated prostate growth resulted in a decrease in total epithelial weight, epithelial cell proliferation, endothelial cell proliferation, and increased epithelial cell apoptosis.	Testosterone	48-60	epidermal growth factor receptor	Rattus norvegicus	14-18	
17252557-6	2007	CONCLUSIONS: This study suggests that increased EGFR signaling during castration mediates stimulatory effects balancing castration-induced prostate regression, and that EGFR signaling is a necessary component in testosterone-stimulated prostate growth.	Testosterone	212-224	epidermal growth factor receptor	Rattus norvegicus	48-52	
17252557-6	2007	CONCLUSIONS: This study suggests that increased EGFR signaling during castration mediates stimulatory effects balancing castration-induced prostate regression, and that EGFR signaling is a necessary component in testosterone-stimulated prostate growth.	Testosterone	212-224	epidermal growth factor receptor	Rattus norvegicus	169-173