PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18545997-10	2009	RESULTS: Among the cells HSC-3 and BHY cells were found most CDDP-sensitive and CDDP-resistant, respectively.	Cisplatin	61-65	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	25-30	
18545997-10	2009	RESULTS: Among the cells HSC-3 and BHY cells were found most CDDP-sensitive and CDDP-resistant, respectively.	Cisplatin	80-84	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	25-30	
18545997-11	2009	The most CDDP-sensitive HSC-3 cells exhibited an increased intracellular cisplatin accumulation, high Na(+),K(+)-ATPase activity and over-expressed Na(+),K(+)-ATPase alpha and beta subunits, ATP7A and ATP7B, compared to the most CDDP-resistant BHY cells, but there were no such differences between the two in the CDDP efflux level or Cu(2+)-ATPase activity.	Cisplatin	9-13	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	24-29	
18545997-11	2009	The most CDDP-sensitive HSC-3 cells exhibited an increased intracellular cisplatin accumulation, high Na(+),K(+)-ATPase activity and over-expressed Na(+),K(+)-ATPase alpha and beta subunits, ATP7A and ATP7B, compared to the most CDDP-resistant BHY cells, but there were no such differences between the two in the CDDP efflux level or Cu(2+)-ATPase activity.	Cisplatin	73-82	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	24-29	
18545997-11	2009	The most CDDP-sensitive HSC-3 cells exhibited an increased intracellular cisplatin accumulation, high Na(+),K(+)-ATPase activity and over-expressed Na(+),K(+)-ATPase alpha and beta subunits, ATP7A and ATP7B, compared to the most CDDP-resistant BHY cells, but there were no such differences between the two in the CDDP efflux level or Cu(2+)-ATPase activity.	Cisplatin	229-233	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	24-29	
18545997-11	2009	The most CDDP-sensitive HSC-3 cells exhibited an increased intracellular cisplatin accumulation, high Na(+),K(+)-ATPase activity and over-expressed Na(+),K(+)-ATPase alpha and beta subunits, ATP7A and ATP7B, compared to the most CDDP-resistant BHY cells, but there were no such differences between the two in the CDDP efflux level or Cu(2+)-ATPase activity.	Cisplatin	229-233	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	24-29	
10680594-2	2000	Cisplatin induced apoptosis in HNSCC cell lines, HSC-2, HSC-3 and HSC-4 in a dose-dependent manner.	Cisplatin	0-9	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	56-61	
17982671-2	2007	Previously, we have reported that the combination of suberoylanilide hydroxamic acid (SAHA), a newly developed histone deacetylase inhibitor, with cisplatin (CDDP) possessed synergistic cytotoxicity against human oral squamous cell carcinoma (OSCC) cell line HSC-3.	Cisplatin	147-156	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	259-264	
17982671-2	2007	Previously, we have reported that the combination of suberoylanilide hydroxamic acid (SAHA), a newly developed histone deacetylase inhibitor, with cisplatin (CDDP) possessed synergistic cytotoxicity against human oral squamous cell carcinoma (OSCC) cell line HSC-3.	Cisplatin	158-162	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	259-264	
17982671-4	2007	Treatment with CDDP or 5-FU either alone or in combination with Zeb or SAHA continued for 48 or 72 h. In HSC-3 cells, Zeb had chemosensitive efficacy with CDDP, but not 5-FU, whereas SAHA showed efficacy with both CDDP and 5-FU.	Cisplatin	15-19	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	105-110	
17390020-1	2007	In the present study, the precise mechanism of the enhancing action of histone deacetylase (HDAC) inhibitors on cisplatin (CDDP)-induced apoptosis was investigated using suberoylanilide hydroxamic acid (SAHA) in human oral squamous cell carcinoma cells (HSC-3).	Cisplatin	112-121	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	254-259	
17390020-1	2007	In the present study, the precise mechanism of the enhancing action of histone deacetylase (HDAC) inhibitors on cisplatin (CDDP)-induced apoptosis was investigated using suberoylanilide hydroxamic acid (SAHA) in human oral squamous cell carcinoma cells (HSC-3).	Cisplatin	123-127	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	254-259	
18383853-1	2008	We established the optimal conditions for the induction of cell death by cisplatin (CDDP) and 5-fluorouracil (5-FU) in human oral squamous cell carcinoma (HSC-2, HSC-3, HSC-4) and human hepatocellular carcinoma (HepG2) cell lines.	Cisplatin	84-88	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	162-167	
18383853-2	2008	HSC-3 cells were the most sensitive to 48 hours" continuous treatment with CDDP, followed by HepG2, HSC-2 and HSC-4 cells.	Cisplatin	75-79	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	0-5	
18383853-4	2008	CDDP induced internucleosomal DNA fragmentation in HSC-2 and HSC-3 cells, but not in HSC-4 cells, while 5-FU failed to induce internucleosomal DNA fragmentation in all of these cells.	Cisplatin	0-4	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	61-66	
18383853-5	2008	The treatment of HSC-2, HSC-3 and HSC-4cells with CDDP for 12 hours (followed by incubation for 36 hours without CDDP) showed comparable magnitude of cytotoxicity and caspase-3 activation with that attained by continuous 48-hour CDDP treatment.	Cisplatin	50-54	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	24-29	
17390020-8	2007	Thus, SAHA appears to disrupt the intracellular redox balance, which causes maximal apoptosis at the G0/G1 phase arrested by CDDP in HSC-3 cells.	Cisplatin	125-129	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	133-138	
29048671-8	2017	Furthermore, CMVpp65-CTL cytotoxicity to CDDP-resistant OSCC cells, HSC-3/CDDP-R1, was the same as the cytotoxicity to the parental cells.	Cisplatin	41-45	DnaJ heat shock protein family (Hsp40) member B7	Homo sapiens	68-73