PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 26859293-6 2016 Inhibition of autophagy by inhibitors or knockdown of Atg5 cancels galectin-1-induced cisplatin resistance in HCC cells. Cisplatin 86-95 HCC Homo sapiens 110-113 26859293-8 2016 Finally, using an in situ hepatoma mouse model, we clearly demonstrated that inhibition of galectin-1 by thiodigalactoside could significantly augment the anti-HCC effect of cisplatin. Cisplatin 174-183 HCC Homo sapiens 160-163 26859293-9 2016 Taken together, our findings offer a new insight into the chemoresistance galectin-1 causes against cisplatin treatment, and points to a potential approach to improve the efficacy of cisplatin in the treatment of HCC patients. Cisplatin 183-192 HCC Homo sapiens 213-216 26754678-2 2016 This prospective multicenter trial assessed the efficacy of hepatic arterial infusion chemoembolization therapy with cisplatin suspended in lipiodol combined with 5-fluorouracil for HCC patients with portal vein tumor thrombosis. Cisplatin 117-126 HCC Homo sapiens 182-185 26754678-12 2016 CONCLUSIONS: Hepatic arterial infusion chemoembolization therapy with cisplatin suspension in lipiodol combined with 5-fluorouracil is effective treatment for unresectable HCC with portal vein tumor thrombosis. Cisplatin 70-79 HCC Homo sapiens 172-175 21748762-4 2011 Interestingly, CypB protected tumor cells, even p53-defective HCC cells, against hypoxia- and cisplatin-induced apoptosis. Cisplatin 94-103 HCC Homo sapiens 62-65 31072375-2 2019 Cisplatinum, a well-known chemotherapeutic drug, has been widely used for treatment of numerous human cancers including HCC. Cisplatin 0-11 HCC Homo sapiens 120-123 31072375-3 2019 This study aimed to investigate the differential expressions of LncRNAs in HCC cells treated with cisplatinum and its underlying mechanism. Cisplatin 98-109 HCC Homo sapiens 75-78 31072375-4 2019 METHODS: The differential expressions of LncRNAs in HCC cells treated with cisplatinum were determined by RNA-seq. Cisplatin 75-86 HCC Homo sapiens 52-55 31072375-9 2019 RESULTS: LncRNA TPTEP1 was highly expressed in cisplatinum-treated HCC cells, which sensitizes hepatocellular carcinoma cell to cisplatinum-induced apoptosis. Cisplatin 47-58 HCC Homo sapiens 67-70 31072375-9 2019 RESULTS: LncRNA TPTEP1 was highly expressed in cisplatinum-treated HCC cells, which sensitizes hepatocellular carcinoma cell to cisplatinum-induced apoptosis. Cisplatin 128-139 HCC Homo sapiens 67-70 28219642-1 2017 Cisplatin is a main compound for human hepatocellular carcinoma (HCC) chemotherapies, but it has certain cytotoxicity during applications. Cisplatin 0-9 HCC Homo sapiens 39-69 28219642-4 2017 In order to investigate whether combination usage of RA and cisplatin can be priority to the later drug"s effect development and its toxicity reduction in HCC, both of two drugs were treated 24 h or 48 h in QGY-7703 cells for estimating their abilities in tumor cell proliferation inhibition. Cisplatin 60-69 HCC Homo sapiens 155-158 28219642-9 2017 All these consequences reflect RA plays an important role in enhancing the therapeutic effect of cisplatin in HCC. Cisplatin 97-106 HCC Homo sapiens 110-113 16396674-8 2006 CONCLUSION: Combination chemotherapy with doxorubicin, cisplatin and capecitabine produced modest antitumor activity with tolerable adverse effects in patients with metastatic HCC. Cisplatin 55-64 HCC Homo sapiens 176-179 12138235-8 2002 CONCLUSIONS: Intra-arterial chemotherapy using cisplatin and etoposide seems to have some anti-tumor effect against advanced HCC, although a high rate of life- threatening complications precludes the indication of this regimen at least for patients with non-compensated cirrhosis. Cisplatin 47-56 HCC Homo sapiens 125-128