{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["7(12)"],"submitter":["Ketola K"],"pubmed_abstract":["<h4>Background</h4>Current treatment options for castration- and treatment-resistant prostate cancer are limited and novel approaches are desperately needed. Our recent results from a systematic chemical biology sensitivity screen covering most known drugs and drug-like molecules indicated that aldehyde dehydrogenase inhibitor disulfiram is one of the most potent cancer-specific inhibitors of prostate cancer cell growth, including TMPRSS2-ERG fusion positive cancers. However, the results revealed that disulfiram alone does not block tumor growth in vivo nor induce apoptosis in vitro, indicating that combinatorial approaches may be required to enhance the anti-neoplastic effects.<h4>Methods and findings</h4>In this study, we utilized a chemical biology drug sensitivity screen to explore dis"],"journal":["PloS one"],"pagination":["e51470"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3520796"],"repository":["biostudies-literature"],"pubmed_title":["Chemical biology drug sensitivity screen identifies sunitinib as synergistic agent with disulfiram in prostate cancer cells."],"pmcid":["PMC3520796"],"pubmed_authors":["Kallioniemi O","Ketola K","Iljin K"],"additional_accession":[]},"is_claimable":false,"name":"Chemical biology drug sensitivity screen identifies sunitinib as synergistic agent with disulfiram in prostate cancer cells.","description":"<h4>Background</h4>Current treatment options for castration- and treatment-resistant prostate cancer are limited and novel approaches are desperately needed. Our recent results from a systematic chemical biology sensitivity screen covering most known drugs and drug-like molecules indicated that aldehyde dehydrogenase inhibitor disulfiram is one of the most potent cancer-specific inhibitors of prostate cancer cell growth, including TMPRSS2-ERG fusion positive cancers. However, the results revealed that disulfiram alone does not block tumor growth in vivo nor induce apoptosis in vitro, indicating that combinatorial approaches may be required to enhance the anti-neoplastic effects.<h4>Methods and findings</h4>In this study, we utilized a chemical biology drug sensitivity screen to explore dis","dates":{"release":"2012-01-01T00:00:00Z","publication":"2012","modification":"2025-04-26T19:53:28.523Z","creation":"2019-03-26T23:19:14Z"},"accession":"S-EPMC3520796","cross_references":{"pubmed":["23251544"],"doi":["10.1371/journal.pone.0051470"]}}