PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
34861633-2	2022	In this study, we employed Langmuir monolayers of a mixture of phospholipids and cholesterol (MIX) as models for tumor cell membranes and investigated their interaction with the anticancer drugs cisplatin (CDDP) and doxorubicin (DOX).	Cisplatin	195-204	Mix paired-like homeobox	Homo sapiens	94-97	
34861633-3	2022	We found that both DOX and CDDP expand and affect the elasticity of MIX monolayers, but these effects are hindered when glutathione-s-transferase (GST) and its cofactor glutathione (GSH) are incorporated.	Cisplatin	27-31	Mix paired-like homeobox	Homo sapiens	68-71	
34861633-4	2022	Changes are induced by DOX or CDDP on the polarization-modulated infrared reflection absorption spectroscopy (PM-IRRAS) data for MIX/GST/GSH monolayers, thus denoting some degree of interaction that is not sufficient to alter the monolayer mechanical properties.	Cisplatin	30-34	Mix paired-like homeobox	Homo sapiens	129-132	
31353575-6	2019	Furthermore, we demonstrated that MIX enhances antiproliferative effect of common cytostatics: 5-fluorouracil and cisplatin.	Cisplatin	114-123	Mix paired-like homeobox	Homo sapiens	34-37	
31353575-12	2019	Furthermore, activity of the substances combined as MIX to influence antiproliferative potential of commonly used in colon cancer treatment cytostatics, 5-fluorouracil, and cisplatin was verified.	Cisplatin	173-182	Mix paired-like homeobox	Homo sapiens	52-55