PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26574916-8	2016	In vitro, testosterone increased expression of cell cycle regulators (cyclin D1, cyclin E, and cyclin-dependent kinase 2) and reduced p53 and p21, which enhanced hepatocyte viability.	Testosterone	10-22	transformation related protein 53, pseudogene	Mus musculus	134-137	
32199951-6	2020	P53/JNK pathway blockade ameliorated the Cd-induced inhibition of steroidogenic acute regulatory protein (STAR) expression and testosterone synthesis.	Testosterone	127-139	transformation related protein 53, pseudogene	Mus musculus	0-3	
28554727-0	2017	Testosterone modulates FoxO3a and p53-related genes to protect C2C12 skeletal muscle cells against apoptosis.	Testosterone	0-12	transformation related protein 53, pseudogene	Mus musculus	34-37	
28554727-3	2017	Since we have observed that testosterone reduces p-p53 and maintains the inactive state of FoxO3a transcription factor, induced by H2O2, we analyzed if the hormone was exerting its antiapoptotic effect at transcriptional level, by modulating pro and antiapoptotic genes associated to them.	Testosterone	28-40	transformation related protein 53, pseudogene	Mus musculus	51-54	
26703444-0	2016	Effect of testosterone on the regulation of p53 and p66Shc during oxidative stress damage in C2C12 cells.	Testosterone	10-22	transformation related protein 53, pseudogene	Mus musculus	44-47	
26703444-4	2016	Testosterone treatment, prior to H2O2, reduces not only p53 phosphorylation but also p66Shc expression, activation and its mitochondrial localization, at the same time that it prevents the mPTP opening.	Testosterone	0-12	transformation related protein 53, pseudogene	Mus musculus	56-59	
26703444-6	2016	Thus, the mPTP opening, p53, JNK and PKCbetaI activation, as well as p66Shc mRNA increase, induced by oxidative stress, were reduced by testosterone pretreatment.	Testosterone	136-148	transformation related protein 53, pseudogene	Mus musculus	24-27	
18030663-6	2007	Results of western blot analysis showed that [6]-gingerol upregulated the testosterone depleted levels of p53 in mouse prostate and upregulated its downstream regulator Bax and further activated Caspase-9 and Caspase-3 in both LNCaP cells and in mouse prostate.	Testosterone	74-86	transformation related protein 53, pseudogene	Mus musculus	106-109