PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26683770-4	2016	We found that DPT induced glioma cell death in vitro and inhibited the growth of xenograft glioma in vivo, which was accompanied with parthanatos-related biochemical events including expressional upregulation of PARP-1, cytoplasmic accumulation of PAR polymer, and nuclear translocation of AIF.	deoxypodophyllotoxin	14-17	poly (ADP-ribose) polymerase family, member 1	Mus musculus	212-218	
26683770-5	2016	In vitro study revealed that genetic knockdown of PARP-1 with small interfering RNA attenuated DPT-induced elevation in the cytoplasmic PAR-polymer and the nuclear AIF, as well as protected glioma cells against the toxicity of DPT.	deoxypodophyllotoxin	95-98	poly (ADP-ribose) polymerase family, member 1	Mus musculus	50-56	
26683770-5	2016	In vitro study revealed that genetic knockdown of PARP-1 with small interfering RNA attenuated DPT-induced elevation in the cytoplasmic PAR-polymer and the nuclear AIF, as well as protected glioma cells against the toxicity of DPT.	deoxypodophyllotoxin	227-230	poly (ADP-ribose) polymerase family, member 1	Mus musculus	50-56	
26683770-6	2016	Further, antioxidant NAC, as well as PARP-1 inhibitor 3AB, not only alleviated the overproduction of ROS caused by DPT, but also reversed the above-mentioned biochemical events, maintained mitochondrial membrane potential and rescued glioma cells death.	deoxypodophyllotoxin	115-118	poly (ADP-ribose) polymerase family, member 1	Mus musculus	37-43