PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
35600955-8	2022	Results: The network pharmacology analysis showed that quercetin, luteolin, and kaempferol are the most significant active components in BHHD; STAT3, Jun, AKT1, MAPK3, MAPK1, and TP53 are the most critical drug targets; regulating hormones, reversing insulin (INS) resistance, exerting anti-inflammatory effects, and improving fertility might be the most important mechanisms of BHHD in the treatment of PCOS.	Luteolin	66-74	tumor protein p53	Homo sapiens	179-183	
22749133-0	2013	The flavonoids diosmetin and luteolin exert synergistic cytostatic effects in human hepatoma HepG2 cells via CYP1A-catalyzed metabolism, activation of JNK and ERK and P53/P21 up-regulation.	Luteolin	29-37	tumor protein p53	Homo sapiens	167-174	
33757400-0	2022	Luteolin Induces Apoptosis and Autophagy in HCT116 Colon Cancer Cells via p53-Dependent Pathway.	Luteolin	0-8	tumor protein p53	Homo sapiens	74-77	
33757400-5	2022	Luteolin at 10 - 20 muM induced cytotoxicity in p53 wild-type HCT116 colon cancer cells but not in p53 mutant HT-29 cells and normal colon cells.	Luteolin	0-8	tumor protein p53	Homo sapiens	48-51	
33757400-7	2022	We identified that luteolin can induce autophagy in p53 wild-type cells but not in p53 mutant cells, suggesting that luteolin-induced autophagy is p53-dependent; however, chloroquine-mediated inhibition of autophagy did not alter cytotoxicity and apoptosis of cells treated with luteolin.	Luteolin	19-27	tumor protein p53	Homo sapiens	52-55	
31383362-9	2019	Also, luteolin induced oxidative stress and ER stress in p53-null Hep3B cells.	Luteolin	6-14	tumor protein p53	Homo sapiens	57-60