PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31900833-6	2020	Treatment of parental Original Article and HQ-selected malignant U937 cells with compound C induced ROS-mediated p38 MAPK activation, leading to a suppression of AMPKalpha, TET2, and FOXP3 expression.	Hydroquinones	43-45	tet methylcytosine dioxygenase 2	Homo sapiens	173-177	
31900833-10	2020	Restoration of AMPKalpha1 or FOXP3 expression increased cell survival after treatment with compound C. In conclusion, our results show that compound C suppresses AMPK/TET2 axis-mediated FOXP3 expression and induces autophagy-dependent apoptosis in parental and HQ-selected malignant U937 cells, suggesting that the AMPK/TET2/FOXP3 axis is a promising target for improving AML therapy and attenuating benzene exposure-induced AML progression.	Hydroquinones	261-263	tet methylcytosine dioxygenase 2	Homo sapiens	167-171